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Results for "

1a

" in MedChemExpress (MCE) Product Catalog:

By Targets:	5-HT Receptor (18) Acyltransferase (1) ADC Cytotoxin (1) Adenosine Receptor (5) Adrenergic Receptor (11) Aldehyde Dehydrogenase (ALDH) (11) Amyloid-β (2) Antibiotic (4) Apoptosis (20) Aurora Kinase (1) Autophagy (6) Bacterial (5) Bcl-2 Family (2) Biochemical Assay Reagents (1) Calcineurin (1) Calcium Channel (1) Cannabinoid Receptor (1) Carboxylesterase (1) Caspase (3) CDK (3) CRFR (1) Cyclophilin (2) DNA Methyltransferase (3) DNA/RNA Synthesis (5) Dopamine Receptor (9) Drug Metabolite (1) Dynamin (1) DYRK (15) EGFR (1) Endogenous Metabolite (3) Epigenetic Reader Domain (3) Fluorescent Dye (1) Fungal (3) GHSR (6) GSK-3 (1) HBV (2) HCV (21) HCV Protease (4) HDAC (2) Histamine Receptor (5) Histone Demethylase (5) HIV (2) HIV Integrase (1) HSP (2) iGluR (2) Influenza Virus (2) Integrin (1) IRE1 (2) Isotope-Labeled Compounds (5) Ligands for E3 Ligase (1) Ligands for Target Protein for PROTAC (1) Liposome (1) Mas-related G-protein-coupled Receptor (MRGPR) (1) mGluR (2) MicroRNA (8) Necroptosis (1) Notch (1) Nucleoside Antimetabolite/Analog (1) Opioid Receptor (1) Oxytocin Receptor (2) p38 MAPK (1) Parasite (5) Phosphatase (1) Phosphodiesterase (PDE) (1) Potassium Channel (3) Prostaglandin Receptor (2) PROTACs (1) Proteasome (1) Ras (3) Reactive Oxygen Species (3) SARS-CoV (9) Sigma Receptor (1) Sirtuin (1) Small Interfering RNA (siRNA) (162) Sodium Channel (15) STING (2) Thyroid Hormone Receptor (1) TMV (1) Toll-like Receptor (TLR) (1) Topoisomerase (1) UGT (2) Vasopressin Receptor (4) VD/VDR (1) Virus Protease (2) γ-secretase (1)
By Research Areas:	Cancer (82) Cardiovascular Disease (7) Endocrinology (16) Infection (44) Inflammation/Immunology (24) Metabolic Disease (20) Neurological Disease (66)
Oligonucleotides:	miRNA mimics (2) miRNA agomirs (2) miRNA antagomirs (2) MicroRNAs (8) Aptamers (1) Pre-designed siRNA Sets (162) Cationic Lipids (1) miRNA inhibitors (2) siRNAs (162)

386

Inhibitors & Agonists

Fluorescent Dye

Biochemical Assay Reagents

Peptides

Inhibitory Antibodies

Natural
Products

485

Recombinant Proteins

Isotope-Labeled Compounds

130

Antibodies

172

Oligonucleotides

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-137584

1a,1b-Dihomo prostaglandin E1 1a,1b-Dihomo PGE1	Prostaglandin Receptor	Endocrinology
1a,1b-Dihomo prostaglandin E1 (1a,1b-Dihomo PGE1) is a class of prostaglandin compound ^[1].

HY-104064

1A-116 5 Publications Verification	Ras Apoptosis	Cancer
1A-116, a potent *Rac1* inhibitor, is specific for W56 residues, can prevent EGF-induced *Rac1* activation and block *Rac1-P-Rex1* interaction. 1A-116 can induce apoptosis and inhibit cell proliferation, migration and cycle progression in a concentration-dependent manner. 1A-116 also demonstrates a high antimetastatic activity in vivo ^[1] .

HY-W128112

1-(a-D-ribofuranosyl)uracil alpha-D-Ribofuranoside,2,4(1H,3H)-pyrimidinedione-1	Nucleoside Antimetabolite/Analog	Cancer
1-(a-D-ribofuranosyl)uracil is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc ^[1].

HY-50202A

Etomoxir sodium salt Maximum Cited Publications 80 Publications Verification (R)-(+)-Etomoxir sodium salt	Apoptosis	Metabolic Disease Cancer
Etomoxir((R)-(+)-Etomoxir) sodium salt is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig ^[1].

HY-131632

1a,1b-Dihomo prostaglandin F2α 1a,1b-Dihomo-PGF2α	Endogenous Metabolite	Others
1a,1b-Dihomo prostaglandin F2α (1a,1b-Dihomo-PGF2α) is the derivative of Prostaglandin F2α (HY-12956) ^[1].

HY-131626

1a,1b-Dihomo prostaglandin E2 1a,1b-Dihomo PGE2	Others	Metabolic Disease
1a,1b-Dihomo Prostaglandin E2 (PGE2) is a rare polyunsaturated fatty acid first identified in extracts of sheep vesicular gland microsomes, known to contain COX, incubated with adrenic acid. 1a,1b-Dihomo PGE2 has also been identified in conditioned media of RAW 264.7 macrophages stimulated with endotoxin and arachidonic acid. This product is thought to be produced by elongation of AA to adrenic acid, which is then metabolized sequentially by COX and PGE synthase.

HY-159675

1-A-N	Liposome	Inflammation/Immunology
1-A-N is a lipid nanoparticle (LNP) used for in vivo delivery of siRNA. 1-A-N can regulate immune response by delivering siCD45 (siRNA targeting CD45) to T cells and silencing the CD45 gene ^[1].

HY-P3915

Esculentin 1A	Bacterial	Infection
Esculentin 1A is a frog skin-derived antimicrobial peptide (AMP) with potent in vitro anti-Pseudomonas activity ^[1].

HY-146483

Anti-Aβ agent 1A	Amyloid-β	Neurological Disease Inflammation/Immunology
Anti-Aβ agent 1A (compound M15) has potent activity against amyloid-β. Anti-Aβ agent 1A possesses can significantly inhibit LPS-induced levels of IL-1β, IL-6 and TNF-α, and reduces the apoptosis of SH-SY5Y induced by H₂O₂ through mitochondria pathway. Anti-Aβ agent 1A possesses antioxidant, anti-inflammatory, anti-Aβ toxicity and neuroprotective activities. Anti-Aβ agent 1A can be used for researching Alzheimer’s disease (AD) ^[1].

HY-108790

Peginterferon beta-1a Peginterferon β-1a	Apoptosis	Neurological Disease Cancer
Peginterferon beta-1a (Peginterferon β-1a) is the first pegylated interferon beta-1a molecule. Peginterferon beta-1a induces cancer cells apoptosis and shows anti-tumor activities in nude mice models. Peginterferon beta-1a can be used for the research of cancer and multiple sclerosis (RMS) ^[1].

HY-100431A

IMR-1A 1 Publications Verification	Notch Drug Metabolite	Cancer
IMR-1A, a acid metabolite of IMR-1, is a Notch inhibitor with an IC₅₀ of 0.5 μM. IMR-1A has a 50-fold increase in potency with respect to IMR-1. IMR-1 can metabolize in vivo to IMR-1A ^[1].

HY-100840

(S)-4C3HPG (S)-4-Carboxy-3-hydroxyphenylglycine	mGluR	Neurological Disease
(S)-4C3HPG ((S)-4-Carboxy-3-hydroxyphenylglycine) is an antagonist of metabotropic glutamate receptor 1a (mGluR 1a) and an agonist of GluR2. (S)-4C3HPG has the anticonvulsant activity and protects against audiogenic seizures in DBA/2 mice ^[1].

HY-P99138

Anti-Mouse IL-1a Antibody (ALF-161)	Integrin	Inflammation/Immunology
Anti-Mouse IL-1a Antibody is an anti-mouse IL-1a IgG1 antibody inhibitor derived from host Armenian Hamster.

HY-136267

HCV-IN-30	HCV	Infection
HCV-IN-30 (compound 48) is a HCV NS5A replication complex inhibitor, with IC₅₀s of 901 and 102 nM for genotypes 1a and 1b replicons, respectively ^[1].

HY-136972

(-)-GB-1a (-)-Biflavanone GB-1a	Others	Others
(-)-GB-1a is a potent antioxidant agent with an IC₅₀ value of 148 µM ^[1].

HY-136532

ZT-1a 1 Publications Verification	Others	Neurological Disease
ZT-1a is a potent, non-ATP-competitive and selective SPAK inhibitor. ZT-1a inhibits SPAK activity with IC₅₀s of 44.3, 35.0, 46.7 μM at ATP concentrations of 0.01, 0.1 and 1 mM, respectively ^[1].

HY-118335

Prazobind SZL 49	Adrenergic Receptor	Neurological Disease
Prazobind (SZL 49), a prazosin analog, is a potent alpha 1-adrenoceptor blocker. Prazobind competes for alpha 1-adrenoceptor binding sites with a similar potency (IC₅₀=1 nM) in tissues enriched in both the alpha 1A (hippocampus) and alpha 1B (liver) subtypes ^[1] .

HY-50202

Etomoxir Maximum Cited Publications 80 Publications Verification (R)-(+)-Etomoxir	Apoptosis	Metabolic Disease Cancer
Etomoxir ((R)-(+)-Etomoxir) is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig.

HY-W420033

(S)-(+)-Etomoxir	Others	Others
(S)-(+)-Etomoxir is the S enantiomer of Etomoxir (HY-50202). Etomoxir is an irreversible inhibitor of carnitine palmitoyltransferase 1a (CPT-1a), inhibits fatty acid oxidation (FAO) through CPT-1a and inhibits palmitate β-oxidation in human, rat and guinea pig ^[1].

HY-131994

STING agonist-16	STING	Infection Cancer
STING agonist-16 (1a) is a specific stimulator of interferon genes (STING) agonist. STING agonist-16 (1a) can be used as a potential antiviral and antitumor tool ^[1].

HY-R02806

mmu-miR-1a-1-5p mimic	MicroRNA	Cancer
mmu-miR-1a-1-5p mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.

mmu-miR-1a-1-5p mimic mmu-miR-1a-1-5p mimic

HY-R02807

mmu-miR-1a-2-5p mimic	MicroRNA	Cancer
mmu-miR-1a-2-5p mimics are small, chemically synthesized double-stranded RNAs that mimic endogenous miRNAs and enable miRNA functional analysis by up-regulation of miRNA activity.

mmu-miR-1a-2-5p mimic mmu-miR-1a-2-5p mimic

HY-164220

PPM1A-IN-1	Phosphatase Bacterial	Infection
PPM1A-IN-1 (Compound IV-4) is an inhibitor for PP2C Ser/Thr phosphatase protein phosphatase Mg2+/Mn2+-dependent 1A. PPM1A-IN-1 exhibits antibacterial activity against Mycobacterium tuberculosis ^[1].

HY-15522

WAY-267464	Oxytocin Receptor	Neurological Disease
WAY-267464 is a non-peptide oxytocin receptor (OTR) agonist. WAY-267464 can impair social recognition memory in rats through a vasopressin 1A receptor antagonist action. WAY-267464 can be used for the research of psychiatric disorders, such disorders include autism spectrum disorder, schizophrenia, and social anxiety disorder ^[1].

HY-157448

CBR1-IN-6	Apoptosis	Cancer
CBR1-IN-6 (compound 1a) is a *CBR1* inhibitor with chemosensitizing and cardioprotective activities ^[1].

HY-RI02806

mmu-miR-1a-1-5p inhibitor	MicroRNA	Cancer
mmu-miR-1a-1-5p inhibitors are chemically-modified oligonucleotides that hybridize with mature miRNAs. The miRNA inhibitors have full-length nucleotide 2'-methoxy modification. The miRNA inhibitors strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes, thereby inhibiting miRNAs from functioning.

mmu-miR-1a-1-5p inhibitor mmu-miR-1a-1-5p inhibitor

HY-RI02807

mmu-miR-1a-2-5p inhibitor	MicroRNA	Cancer
mmu-miR-1a-2-5p inhibitors are chemically-modified oligonucleotides that hybridize with mature miRNAs. The miRNA inhibitors have full-length nucleotide 2'-methoxy modification. The miRNA inhibitors strongly compete with mature miRNAs to prevent the complementary pairing of miRNAs and their target genes, thereby inhibiting miRNAs from functioning.

mmu-miR-1a-2-5p inhibitor mmu-miR-1a-2-5p inhibitor

HY-12294

PEAQX NVP-AAM077	Caspase Apoptosis iGluR	Neurological Disease
PEAQX (NVP-AAM077) is an orally active and selective NMDA antagonist, with IC₅₀ values of 270 nM and 29.6 μM for hNMDAR 1A/2A and hNMDAR 1A/2B, respectively. PEAQX can promote the activation of caspase-3 and induce cell apoptosis in cortical striatal slice cultures ^[1] .

HY-U00433

JMV 2959 2 Publications Verification	GHSR	Neurological Disease Endocrinology
JMV 2959 is a growth hormone secretagogue receptor type 1a (GHS-R_1a) antagonist with an IC₅₀ of 32 nM.

HY-161978

CDK4/6-IN-22	CDK	Cancer
CDK4/6-IN-22 (Compound 1-A) is a CDK4 and CDK6 dual inhibitor ^[1].

HY-149694

Aurora kinase inhibitor-12	Aurora Kinase	Cancer
Aurora Kinase Inhibitor-12 (Compound 1a ) is the inhibitor of aurora kinase which is a key enzyme that is implicated in tumor growth ^[1].

HY-129314

CM-39	Aldehyde Dehydrogenase (ALDH)	Cancer
CM-39 is a non-covalent and reversible inhibitor for aldehyde dehydrogenase 1A (ALDH1A) with an IC₅₀ of 0.9 μM ^[1].

HY-12782T

Iadademstat dihydrochloride 3 Publications Verification ORY-1001 dihydrochloride; RG6016 dihydrochloride; RO 7051790 dihydrochloride	Histone Demethylase	Cancer
Iadademstat (ORY-1001) dihydrochloride is a selective irreversible lysine (K)-specific demethylase 1A (KDM1A/LSD1) inhibitor.

HY-115938

BEC2	Others	Metabolic Disease
BEC2 is an ester derivative of Baicalin, with good lipid-lowering activity. BEC2 can direct activate the carnitine palmitoyltransferase 1A (CPT1A) ^[1].

HY-147060

Dyrk1A-IN-3	DYRK	Neurological Disease
Dyrk1A-IN-3 (Compound 8b), a highly selective dual-specificity tyrosine-regulated kinase 1A (DYRK1A) inhibitor, maintains high levels of DYRK1A binding affinity (IC₅₀=76 nM). Dyrk1A-IN-3 can be used for the research of neurodegenerative disorders such as Alzheimer’s Disease, Huntington’s Disease, and Parkinson’s Disease ^[1].

HY-115995

Antitumor agent-50	Others	Cancer
Antitumor agent-50 (compound 1a), a thiazolidinone, is a potent antitumor agent. Antitumor agent-50 has the potential for osteosarcoma (OS) research ^[1].

HY-150074

STING agonist-18	Others	Cancer
STING agonist-18 (compound 1a) can be used for synthesis of antibody-drug conjugates (ADCs), such Trastuzumab (HY-P9907) conjugate ^[1].

HY-19880

RWJ-676070	Vasopressin Receptor	Endocrinology
RWJ-676070 is a dual vasopressin V(1A)/V(2) receptor antagonist with an K_i value of 1.4 nM and 14 nM respectly ^[1].

HY-112078

(S,R,S)-AHPC-Me VHL ligand 2; E3 ligase Ligand 1a	Ligands for E3 Ligase	Cancer
(S,R,S)-AHPC-Me (VHL ligand 2) is the (S,R,S)-AHPC-based VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein ^[1]. (S,R,S)-AHPC-Me can be used to synthesize ARV-771, a von Hippel-Landau (VHL) E3 ligase-based BET PROTAC degrader. ARV-771 potently degrades BET protein in castration-resistant prostate cancer (CRPC) cells with a DC₅₀ <1 nM .

HY-12294A

PEAQX tetrasodium hydrate 5 Publications Verification NVP-AAM077 tetrasodium hydrate	Apoptosis Caspase iGluR	Neurological Disease
PEAQX tetrasodium hydrate (NVP-AAM077 tetrasodium hydrate) is a tetrasodium hydrate of PEAQX (HY-12294). PEAQX tetrasodium hydrate is an orally active and selective NMDA antagonist, with IC₅₀ values of 270 nM and 29.6 μM for hNMDAR 1A/2A and hNMDAR 1A/2B, respectively. PEAQX tetrasodium hydrate can promote the activation of caspase-3 and induce cell apoptosis in cortical striatal slice cultures ^[1] .

HY-19612B

DDP-38003 trihydrochloride	Histone Demethylase	Cancer
DDP-38003 trihydrochloride is an novel, orally available inhibitor of histone lysine-specific demethylase 1A (KDM1A/LSD1) with an IC₅₀ of 84 nM.

HY-150074A

STING agonist-18 diTFA	Others	Cancer
STING agonist-18 diTFA (compound 1a) can be used for synthesis of antibody-drug conjugates (ADCs), such Trastuzumab (HY-P9907) conjugate ^[1].

HY-12981

RG7713 2 Publications Verification RO5028442	Vasopressin Receptor	Neurological Disease Endocrinology
RG7713 (RO5028442) is a highly potent and selective Brain-Penetrant Vasopressin 1a (V1a) receptor antagonist with K_is of 1 nM (hV1a) and 39 nM (mV1a).

HY-U00433A

JMV 2959 hydrochloride 2 Publications Verification	GHSR	Neurological Disease Endocrinology
JMV 2959 hydrochloride is a growth hormone secretagogue receptor type 1a (GHS-R_1a) antagonist with an IC₅₀ of 32±3 nM in LLC-PK₁ cells.

HY-19612A

DDP-38003 dihydrochloride	Histone Demethylase	Cancer
DDP-38003 dihydrochloride is an novel, orally available inhibitor of histone lysine-specific demethylase 1A (KDM1A/LSD1) with an IC₅₀ of 84 nM ^[1].

HY-D1453

Immune initiator-1	Biochemical Assay Reagents	Cancer
Immune initiator-1 (Compound 1a) is an amino acid-modified near-infrared Aza-BODIPY photosensitizer, acts as an immune initiator for potent photodynamic research in melanoma ^[1].

HY-12369

GGTI-2133	Others	Inflammation/Immunology
GGTI-2133 is an inhibitor for geranylgeranyltransferase I (GGTase-I) with an IC₅₀ of 38 nM. GGTI-2133 inhibits the geranylation of *Rap-1A* with an IC₅₀ of 10 μM ^[1].

HY-118932

HCV-IN-45	HCV	Infection
HCV-IN-45 (Compound EI-1) is an inhibitor for hepatitis C virus (HCV), that inhibits 1a and 1b HCV pseudoparticles with EC₅₀ of 0.134 and 0.027 μM. HCV-IN-45 inhibits 1a/2a and 1b/2a cell culture-adapted HCV (HCVcc), with EC₅₀ of 0.024 and 0.012μM. HCV-IN-45 inhibits the entry of the virus into hepatocyte, and blocks the cell-cell spread ^[1].

HY-12731

GSK2236805	HCV	Infection
GSK2236805 is a potent hepatitis C virus inhibitor with pEC₅₀ values of 10.4, 11.1 for HCV genotype 1a (gt1a) and gt1b, respectively ^[1].

HY-R02806A

mmu-miR-1a-1-5p agomir	MicroRNA	Cancer
mmu-miR-1a-1-5p agomirs are chemically-modified double-strand miRNA mimics with modified mature miRNA strand: 2 phosphorothioates at the 5' end, 4 phosphorothioates at the 3' end, 3' end cholesterol group, and full-length nucleotide 2'-methoxy modification. They are designed to mimic endogenous miRNAs and recommended for miRNA functional studies. Compared with miRNA mimics, they exhibits enhanced cellular uptake, stability and regulatory activity in vivo.

mmu-miR-1a-1-5p agomir mmu-miR-1a-1-5p agomir

Cat. No.	Product Name	Type

HY-159114

Whole Glucan Particles	Carbohydrates
Whole Glucan Particles is a *Dectin-1a* agonist. Whole Glucan Particles activates the innate immune system to improve the function of macrophages, monocytes and other immune cells ^[1].

HY-E70140

α-1,4-N-Acetylglucosaminyltransferase 4 EC 2.4.1; A4GNT	Enzyme Substrates
α-1,4-N-Acetylglucosaminyltransferase 4 (EC 2.4.1, A4GNT) catalyzes the transfer of N-acetylglucosamine (GlcNAc) to core 2 branched O-glycans and suppresses H. pylori growth ^[1].

HY-158458

A2[3]G1F1(α-1-3) glycan A2[3]G1F1(a1-3) glycan	Carbohydrates
A2[3]G1F1(α-1-3) glycan (A2[3]G1F1(a1-3) glycan) is an asymmetric Lewis X polysaccharide and N-glycan. SLeX is a ligand for the cell adhesion molecule E-selectin, which is specifically expressed at sites of inflammatory lesions. Designing SLeX-polysaccharide conjugates to deliver drugs to inflammatory lesions ^[1].

Cat. No.	Product Name	Target	Research Area

HY-N11615

Cyclo(Pro-Val)	Peptides	Others
Cyclo(Pro-Val) can be isolated from Pseudomonas fluorescens GcM5-1A and has cytotoxicity ^[1].

HY-19884B

Relamorelin TFA RM-131 TFA; BIM-28131 TFA	GHSR	Metabolic Disease
Relamorelin (RM-131) TFA, a pentapeptide ghrelin analog, is a selective ghrelin/growth hormone secretagogue receptor (GHSR) agonist with a K_i of 0.42 nM for *GHS-1a* receptor. Relamorelin TFA is centrally penetrant. Relamorelin TFA increases growth hormone levels and accelerates gastric emptying. Relamorelin TFA has the potential for cachexia, gastroparesis, and gastric/intestinal dysmobility disorders research ^[1] .

HY-P1411

Psalmotoxin 1 1 Publications Verification PcTx1; Psalmopoeus cambridgei toxin-1	Sodium Channel Apoptosis	Neurological Disease Cancer
Psalmotoxin 1 (PcTx1) is a protein toxin that can bind at subunit-subunit interfaces of acid-sensing ion channel 1a (ASIC1a). Psalmotoxin 1 is a potent and slective ASIC1a inhibitor (IC₅₀: 0.9 nM) by increasing the apparent affinity for H ⁺ of ASIC1a. Psalmotoxin 1 can induce cell apoptosis, also inhibits cell migration, proferliration and invasion of cancer cells. Psalmotoxin 1 can be used in the research of cancers, or neurological disease ^[1] .

HY-P3915

Esculentin 1A	Bacterial	Infection
Esculentin 1A is a frog skin-derived antimicrobial peptide (AMP) with potent in vitro anti-Pseudomonas activity ^[1].

HY-P5176

Latartoxin-1a LtTx-1a	Peptides	Neurological Disease
Latartoxin-1a (LtTx-1a) is a peptide toxin can be isolated from L. tarabaevi. Latartoxin-1a is paralytic and lethal to insects and has membrane-bound activity ^[1].

HY-P1610

Asudemotide	Peptides	Cancer
Asudemotide (S-588410) is a peptide of human DEP domain-containing protein 1A. Asudemotide is an immunostimulant. Asudemotide has a sequence of H-Glu-Tyr-Tyr-Glu-Leu-Phe-Val-Asn-Ile-OH. Asudemotide induces a tumor immune response in esophageal cancer. ^[1].

HY-P5780

π-TRTX-Hm3a	Sodium Channel	Neurological Disease
π-TRTX-Hm3a is a 37-amino acid peptide isolated from Togo starburst tarantula (Heteroscodra maculata) venom. π-TRTX-Hm3a pH-dependently inhibits acid-sensing ion channel 1a (ASIC1a) with an IC₅₀ of 1-2 nM and potentiates *ASIC1b* with an EC₅₀ of 46.5 nM ^[1].

HY-19884

Relamorelin RM-131; BIM-28131	GHSR	Metabolic Disease
Relamorelin (RM-131), a pentapeptide ghrelin analog, is a selective ghrelin/growth hormone secretagogue receptor (GHSR) agonist with a K_i of 0.42 nM for *GHS-1a* receptor. Relamorelin is centrally penetrant. Relamorelin increases growth hormone levels and accelerates gastric emptying. Relamorelin has the potential for cachexia, gastroparesis, and gastric/intestinal dysmobility disorders research ^[1] .

HY-19884A

Relamorelin acetate RM-131 acetate; BIM-28131 acetate	GHSR	Metabolic Disease
Relamorelin (RM-131) acetate, a pentapeptide ghrelin analog, is a selective ghrelin/growth hormone secretagogue receptor (GHSR) agonist with a K_i of 0.42 nM for *GHS-1a* receptor. Relamorelin acetate is centrally penetrant. Relamorelin acetate increases growth hormone levels and accelerates gastric emptying. Relamorelin acetate has the potential for cachexia, gastroparesis, and gastric/intestinal dysmobility disorders research ^[1] .

HY-P4542

(D-Phe12,Nle21,38,α-Me-Leu37)-CRF (12-41) (human, rat)	CRFR	Endocrinology
(D-Phe12,Nle21,38,α-Me-Leu37)-CRF (12-41) (human, rat) is a CRF antagonist. (D-Phe12,Nle21,38,α-Me-Leu37)-CRF (12-41) (human, rat) prevents the IL-1a induced Luteinizing hormone (LH) inhibition ^[1].

HY-P1411A

Psalmotoxin 1 TFA 1 Publications Verification PcTx1 TFA; Psalmopoeus cambridgei toxin-1 TFA	Sodium Channel Apoptosis	Neurological Disease Cancer
Psalmotoxin 1 (PcTx1) TFA is a protein toxin that can bind at subunit-subunit interfaces of acid-sensing ion channel 1a (ASIC1a). Psalmotoxin 1 TFA is a potent and slective ASIC1a inhibitor (IC₅₀: 0.9 nM) by increasing the apparent affinity for H ⁺ of ASIC1a. Psalmotoxin 1 TFA can induce cell apoptosis, also inhibits cell migration, proferliration and invasion of cancer cells. Psalmotoxin 1 TFA can be used in the research of cancers, or neurological disease ^[1] .

HY-P5865

Tap1a Theraphotoxin-Tap1a; TRTX-Tap1a; µ/ω-TRTX-Tap1a	Sodium Channel	Neurological Disease
Tap1a (Theraphotoxin-Tap1a) is a spider venom peptide that inhibits sodium channels with IC₅₀s of 80 nM and 301 nM against Na_v1.7 and Na_v1.1, respectively. Tap1a shows analgesic effects ^[1].

HY-P5813

Cd1a β-TRTX-cd1a; β-Theraphotoxin-cd1a	Peptides	Neurological Disease
Cd1a is a β-toxin derived from the African spider Ceratogyrus darlingi. Cd1a can regulate calcium ion channels. Cd1a inhibits human calcium ion channels (Ca_v2.2)(IC₅₀2.6 μM) and mouse sodium ion channels (Na_v1.7). Cd1a can be used in the development of peripheral pain treatment drugs ^[1].

HY-P5801

Phlo1a μ-TrTx-Phlo1a	Sodium Channel	Neurological Disease
Phlo1a (μ-TrTx-Phlo1a) is a peptide toxin contains 35-amino acid residues. Phlo1b is a selective *Nav1.7* inhibitor. Phlo1a has a weak inhibitory effect on Nav1.2 and Nav1.5 ^[1].

HY-P5162

Dc1a	Sodium Channel	Inflammation/Immunology
Dc1a potently promotes opening of the German cockroach Na_v channel (BgNa_v1). Dc1a is a toxin can be isolated from the desert bush spider Diguetia canities ^[1].

HY-P5183

Hm1a	Sodium Channel	Neurological Disease
Hm1a is a disulfide-rich spider-venom peptide, and a *NaV1.1* activator. Hm1a restores the function of inhibitory interneurons in Dravet syndrome (DS) mouse model ^[1].

HY-P5637

Tur1A	Bacterial	Infection
Tur1A is an antimicrobial peptide derived from bottlenose dolphins Tursiops truncates. Tur1A inhibits bacterial protein synthesis by binding to ribosomes and blocking the transition from the initiation stage to the extension stage ^[1].

HY-P2265

SAH-SOS1A	Ras	Cancer
SAH-SOS1A is a peptide-based *SOS1/KRAS* protein interaction inhibitor. SAH-SOS1A binds to wild-type and mutant KRAS (G12D, G12V, G12C, G12S, and Q61H) with nanomolar affinity (EC₅₀=106-175 nM), directly and independently blocks nucleotide association, impairs KRAS-driven cancer cell viability, and exerts its effects by on-mechanism blockade of the ERK-MAPK phosphosignaling cascade downstream of KRAS ^[1].

HY-P2265A

SAH-SOS1A TFA	Ras	Cancer
SAH-SOS1A TFA is a peptide-based *SOS1/KRAS* protein interaction inhibitor. SAH-SOS1A TFA binds to wild-type and mutant KRAS (G12D, G12V, G12C, G12S, and Q61H) with nanomolar affinity (EC₅₀=106-175 nM). SAH-SOS1A TFA directly and independently blocks nucleotide association. SAH-SOS1A TFA impairs KRAS-driven cancer cell viability and exerts its effects by on-mechanism blockade of the ERK-MAPK phosphosignaling cascade downstream of KRAS ^[1].

HY-P3058

Ederimotide WT-1 A1	Peptides	Cancer
Ederimotide(WT-1 A1) can be used as a potential target for studying pancreatic cancer ^[1].

HY-P5790

μ-TRTX-Hd1a	Sodium Channel	Neurological Disease
μ-TRTX-Hd1a, a spider venom, is a selective NaV 1.7 inhibitor. μ-TRTX-Hd1a is a gating modifier that inhibits human NaV 1.7 by interacting with the S3b-S4 paddle motif in channel domain II ^[1].

HY-P5784

δ-Buthitoxin-Hj1a	Sodium Channel	Neurological Disease
δ-Buthitoxin-Hj1a, a scorpion-venom peptide, is a potent *NaV1.1* agonist with an EC₅₀ of 17nM. δ-Buthitoxin-Hj1a can be used for the Dravet syndrome (DS) research ^[1].

HY-P1355

Cyclosporin A-Derivative 1	Calcineurin Cyclophilin	Inflammation/Immunology
Cyclosporin A-Derivative 1 is a crystalline intermediate derived from the opening of cyclosporin A extracted from patent WO 2013167703 A1. Cyclosporin A is an immunosuppressive agent which can bind to the cyclophilin and inhibit calcineurin.

HY-P5782

δ-Theraphotoxin-Hm1a toxin	Sodium Channel	Neurological Disease
δ-Theraphotoxin-Hm1a toxin is a selective *Na_v1.1* activator. δ-Theraphotoxin-Hm1a toxin elicits pain and touch sensitivity. δ-Theraphotoxin-Hm1a toxin can be used for the research of irritable bowel syndrome ^[1].

HY-P5153

ProTx-III μ-TRTX-Tp1a	Sodium Channel	Neurological Disease
ProTx-III is a selective and potent inhibitor of voltage-gated sodium channel *Na_v1.7, with an IC₅₀* of 2.1 nM. ProTx-III is a spider venom peptide isolated from the venom of the Peruvian green velvet tarantella. ProTx-III has a typical inhibitor cystine knot motif (ICK). ProTx-III is able to reverse the pain response. ProTx-III can be used to study diseases such as chronic pain, epilepsy, and arrhythmia ^[1].

HY-P5811

Ceratotoxin-1 CcoTx1; β-TRTX-cm1a	Sodium Channel	Neurological Disease
Ceratotoxin-1 (CcoTx1), a peptide toxin, is an voltage-gated sodium channel subtypes inhibitor. Ceratotoxin-1 inhibits *Nav1.1/β1, Nav1.2/β1, Nav1.4/β1, and Nav1.5/β1* with IC₅₀ of 523 nM, 3 nM, 888 nM, and 323 nM, respectively. Ceratotoxin-1 also inhibits *Nav1.8/β1* ^[1].

HY-P5142

ω-Hexatoxin-Hv1a ω-ACTX-Hv1; ω-Atracotoxin-HV1	Calcium Channel	Neurological Disease
ω-Hexatoxin-Hv1a is a neurotoxin that can be isolated from the venom spider (Hadronyche versuta).ω-Hexatoxin-Hv1a blocks voltage-gated calcium channels ^[1] .

Cat. No.	Product Name	Category	Target	Chemical Structure

HY-P99231

Edrecolomab Panorex; CO17-1a	Classification of Application Fields Disease Research Fields Cancer	Others
Edrecolomab (Panorex) is a murine monoclonal antibody to the cell-surface glycoprotein 17-1A, expressed on epithelial tissues and on various carcinomas. Edrecolomab shows anti-tumor activity and can be used in colorectal carcinoma research ^[1] .

HY-N11615

Cyclo(Pro-Val)	Structural Classification Alkaloids Microorganisms Other Alkaloids Source classification	Others
Cyclo(Pro-Val) can be isolated from Pseudomonas fluorescens GcM5-1A and has cytotoxicity ^[1].

HY-B1167

Ajmaline Cardiorythmine; (+)-Ajmaline	Apocynaceae Cardiovascular Disease Alkaloids Piperidine Alkaloids Structural Classification Rauvolfia serpentina Classification of Application Fields Source classification Plants Disease Research Fields Indole Alkaloids	Sodium Channel
Ajmaline (Cardiorythmine) is a sodium channel blocking, class 1A anti-arrhythmic agent. Ajmaline blocks HERG currents with an IC₅₀ of 1 μM in HEK cells and 42.3 μM in Xenopus oocytes. Ajmaline can be used for the research of the ventricular tachyarrhythmia ^[1] .

HY-N12625

(R)-(+)-O-Demethylbuchenavianine	Structural Classification Alkaloids Flavonoids Flavones Other Alkaloids Buchenavia macrophylla Spruce ex Eichler Combretaceae Source classification Plants	CDK DYRK GSK-3
(R)-(+)-O-Demethylbuchenavianine is an inhibitor for Cyclin-dependent kinases (CDK). (R)-(+)-O-Demethylbuchenavianine inhibits CDK1, CDK5, glycogen synthase kinase-3 (GSK3), cdc2-like kinase (CLK1) and dual specificity tyrosine-phosphorylation-regulated kinase 1A (DYRK1A), with IC₅₀s of 1.1, 0.95, >10, >10 and >10 μM, respectively ^[1].

HY-N6615

Aflatoxin B1 4 Publications Verification	Infection Structural Classification Human Gut Microbiota Metabolites Microorganisms Classification of Application Fields Source classification Endogenous metabolite Disease Research Fields	Apoptosis Reactive Oxygen Species Bcl-2 Family Caspase
Aflatoxin B1 (AFB1) is a Group 1A carcinogen and a secondary metabolite produced by Aspergillus flavus and A. parasiticus. Aflatoxin B1 (AFB1) primarily induces mutations by causing a G to T transversion at the third nucleotide of codon 249 in the tumor suppressor gene p53. In the body, Aflatoxin B1 (AFB1) can cause damage to the intestines and kidneys and has some teratogenic effects ^[1] .

HY-19828

Herboxidiene GEX1a	Microorganisms Classification of Application Fields Ketones, Aldehydes, Acids Source classification Disease Research Fields Biological Pesticide Research Cancer Agricultural Research	DNA/RNA Synthesis
Herboxidiene (GEX1A) is a potent phytotoxic polyketide from Streptomyces sp. A7847 with a diverse range of activities, including herbicidal, anti-cholesterol, anti-tumor effects. Herboxidiene inhibits the pre-mRNA splicing process by binding to spliceosome-associated protein (SAP) 155, a subunit of SF3b, in the splicesome ^[1] .

HY-136972

(-)-GB-1a (-)-Biflavanone GB-1a	Garcinia prainiana King Structural Classification Flavonoids Flavonones Source classification Guttiferae Plants	Others
(-)-GB-1a is a potent antioxidant agent with an IC₅₀ value of 148 µM ^[1].

HY-B1167R

Ajmaline (Standard)	Apocynaceae Alkaloids Piperidine Alkaloids Structural Classification Rauvolfia serpentina Source classification Plants Indole Alkaloids	Sodium Channel
Ajmaline (Standard) is the analytical standard of Ajmaline. This product is intended for research and analytical applications. Ajmaline (Cardiorythmine) is a sodium channel blocking, class 1A anti-arrhythmic agent. Ajmaline blocks HERG currents with an IC₅₀ of 1 μM in HEK cells and 42.3 μM in Xenopus oocytes. Ajmaline can be used for the research of the ventricular tachyarrhythmia ^[1] .

HY-N12697A

Polycarpine hydrochloride	Structural Classification Alkaloids Animals Other Alkaloids Source classification	SARS-CoV Virus Protease Influenza Virus Fungal
Polycarpine hydrochloride (1a) is a broad-spectrum Mpro inhibitor (IC₅₀ = 30 nM) that can be isolated from the Polycarpa aurata and also serves as an anti-coronaviral agent. Polycarpine hydrochloride possesses antiviral and antifungal activities, with IC₅₀ values of 30.0 nM and 0.12 μM against SARS-CoV-2 Mpro and PEDV Mpro, respectively ^[1].

HY-N6615R

Aflatoxin B1 (Standard)	Infection Structural Classification Microorganisms Classification of Application Fields Source classification Phenylpropanoids Endogenous metabolite Disease Research Fields	Bacterial Endogenous Metabolite Parasite
Aflatoxin B1 (Standard) is the analytical standard of Aflatoxin B1. This product is intended for research and analytical applications. Aflatoxin B1 (AFB1) is a Class 1A carcinogen, which is a secondary metabolite of Aspergillus flavus and A. parasiticus. Aflatoxin B1 (AFB1) mainly induces the transversion of G-->T in the third position of codon 249 of the p53 tumor suppressor gene, resulting in mutation ^[1] .

HY-N10985

Xanthone V1a	Structural Classification Flavonoids Maclura fruticosa (Roxburgh) Corner Source classification Plants Moraceae Other Flavonoids	Others
Xanthone V1a has antioxidant activity against the DPPH radical (IC₅₀: 10.43 µM). Xanthone V1a has cytotoxicity against cancer cells ^[1] .

HY-N10511

GM1a Ganglioside oligosaccharide	Structural Classification Natural Products Polysaccharides Classification of Application Fields Endogenous metabolite Inflammation/Immunology Disease Research Fields Saccharides	Others
GM1a Ganglioside oligosaccharide is a semisynthetic form of ganglioside GM1. Ganglioside GM1 is the natural receptor for cholera toxin and plays an important role not only in general growth regulation but also in the coupling of hormone-induced responses ^[1].

HY-123686

Ivermectin B1a monosaccharide	Structural Classification Natural Products Microorganisms Source classification	Parasite
Ivermectin B1a monosaccharide is a modified Ivermectin B1a (HY-126937). Ivermectin B1a monosaccharide is an antiparasite agent with a minimum concentration for full activity in Haemonchus contortus larval development of 0.001 μg/mL ^[1].

HY-15311

Avermectin B1 4 Publications Verification Abamectin; Avermectin B1a-Avermectin B1b mixt.	Structural Classification Classification of Application Fields Source classification Anti-parasitic Antibacterial Disease Research Biological Pesticide Research Agricultural Research Infection Microorganisms Macrolide Antibiotics Antibiotics Animal Husbandry Inflammation/Immunology Disease Research Fields	Parasite Autophagy Apoptosis Reactive Oxygen Species Antibiotic
Avermectin B1 (Abamectin) is a mixture of two similar segments of avermectin. Avermectin B1 is an orally anti-infection agent, which can be used in the research of parasitic worms, insect pests, agriculture and animal husbandry. Avermectin B1 can also induce the production of ROS and induces cytotoxicity, apoptosis and autophagy ^[1] .

Cat. No.	Product Name	Chemical Structure

HY-15602S

Ledipasvir-d6
Ledipasvir-d₆ is the deuterium labeled Ledipasvir. Ledipasvir (GS-5885) is an inhibitor of the hepatitis C virus NS5A, with EC50s of 34 pM and 4 pM against genotype 1a and 1b replicon, respectively. Ledipasvir is also a SARS-CoV 3CLpro inhibitor with an IC50 of 1.62 μM[3].

HY-A0077S1

Perphenazine-d4
Perphenazine-d₄ is the deuterium labeled Perphenazine. Perphenazine is a typical antipsychotic agent, inhibits 5-HT2Areceptor, Alpha-1A adrenergic receptor, Dopamine receptor D2/D3, D2L receptor, and Histamine H1 receptor, with Ki values of 5.6, 10, 0.765/0.13, 3.4, and 8 nM, respectively.

HY-137083S

Trifluoperazine N-glucuronide-d3
Trifluoperazine N-glucuronide-d₃ is deuterium labeled Trifluoperazine N-Glucuronide. Trifluoperazine N-Glucuronide (UGT1A4), as one of the human UGT1A isoforms, is expressed in the liver. Trifluoperazine N-Glucuronide catalyzes the imipramine and trifluoperazine Nglucuronide formation[1].

HY-16567S

Asenapine-13C,d3 hydrochloride
Asenapine- ¹³C,d₃ (hydrochloride) is the ¹³C- and deuterium labeled Asenapine (hydrochloride). Asenapine hydrochloride, an antipsychotic, is a 5-HT (1A, 1B, 2A, 2B, 2C, 5A, 6, 7) and Dopamine (D2, D3, D4) receptor antagonist with Ki values of 0.03-4.0 nM for 5-HT and 1.3, 0.42, 1.1 nM for Dopamine receptor, respectively.

HY-A0077S2

Perphenazine-d6 fumarate

Perphenazine-d6 (fumarate) is a deuterated labeled Perphenazine ^[1]. Perphenazine is an orally active dopamine receptor and histamine-1 receptor antagonist, with K_i values of 0.56 nM (D2), 0.43 nM (D3), 6 nM (5-HT2A), respectively. Perphenazine also binds to Alpha-1A adrenergic receptor. Perphenazine inhibits cancer cell proliferation, and induces apoptosis. Perphenazine can be used in the research of mental disease, cancer, inflammation .

HY-N6615S

Aflatoxin B1-13C17

Aflatoxin B1- ¹³C₁₇ is ¹³C- and ¹⁵N-labeled Aflatoxin B1 (HY-N6615). Aflatoxin B1 (AFB1) is a Group 1A carcinogen and a secondary metabolite produced by Aspergillus flavus and Aspergillus parasiticus. Aflatoxin B1 (AFB1) primarily induces mutations by causing a G to T transversion at the third nucleotide of codon 249 in the tumor suppressor gene p53. In the body, Aflatoxin B1 (AFB1) can cause damage to the intestines and kidneys and has some teratogenic effects ^[1].

HY-113459S

Prostaglandin F1a-d9
Prostaglandin F1a-d₉ is the deuterium labeled Prostaglandin F1a[1].

Cat. No.	Compare	Product Name	Application	Reactivity

HY-P81119

	MTNR1A Antibody MTR1a_HUMAN; Melatonin receptor type 1a; Melatonin Receptor 1a; Mel-1a-R; Mel1a receptor; MT1; MT 1; Mel 1a R	WB, ELISA, IHC-P, IHC-F, ICC/IF	Human, Mouse, Rat
	MTNR1A Antibody is an unconjugated, approximately 39 kDa, rabbit-derived, anti-MTNR1A polyclonal antibody. MTNR1A Antibody can be used for: WB, ELISA, IHC-P, IHC-F, IF expriments in human, mouse, rat, and predicted: chicken, dog, pig, cow, sheep, guinea pig background without labeling.

HY-P82256

	Syntaxin 1A Antibody (YA2001) STX1a; STX1; Syntaxin-1a; Neuron-specific antigen HPC-1	WB, IP, FC	Human, Mouse, Rat
	Syntaxin 1A Antibody (YA2001) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA2001), targeting Syntaxin 1A, with a predicted molecular weight of 33 kDa (observed band size: 33 kDa). Syntaxin 1A Antibody (YA2001) can be used for WB, IP, FC experiment in human, mouse, rat background.

HY-P80848

	Phospho-RSK1 p90 (Ser380) Antibody RPS6KA1; MAPKAPK1a; RSK1; Ribosomal protein S6 kinase alpha-1; S6K-alpha-1; 90 kDa ribosomal protein S6 kinase 1; p90-RSK 1; p90RSK1; p90S6K; MAP kinase-activated protein kinase 1a; MAPK-activated protein kinase 1a; MAPKAP kinase 1a; MAPKAP	WB, ICC/IF, IP	Human, Rat, Mouse
	Phospho-RSK1 p90 (Ser380) Antibody is a non-conjugated and Rabbit origined monoclonal antibody about 83 kDa, targeting to Phospho-RSK1 p90 (Ser380). It can be used for WB, ICC/IF, IP assays with tag free, in the background of Human, Mouse and Rat.

HY-P80712

	Hsp70 1A Antibody (YA727) HSP72; HSPA1; HSP70I; HSPA1B; HSP70-1; HSP70-1a.	WB, IHC-F, IHC-P, ICC/IF	Human, Mouse, Rat
	Hsp70 1A Antibody (YA727) is a non-conjugated and Mouse origined monoclonal antibody about 70 kDa, targeting to Hsp70 1A (1D9). It can be used for WB,IHC-F,IHC-P,ICC/IF assays with tag free, in the background of Human, Mouse, Rat.

HY-P80849

	Phospho-RSK1 p90 (Thr359/Ser363) Antibody RPS6KA1; MAPKAPK1a; RSK1; Ribosomal protein S6 kinase alpha-1; S6K-alpha-1; 90 kDa ribosomal protein S6 kinase 1; p90-RSK 1; p90RSK1; p90S6K; MAP kinase-activated protein kinase 1a; MAPK-activated protein kinase 1a; MAPKAP kinase 1a; MAPKAP	WB, IP	Human, Mouse, Rat
	Phospho-RSK1 p90 (Thr359/Ser363) Antibody is a non-conjugated and Rabbit origined monoclonal antibody about 83 kDa, targeting to Phospho-RSK1 p90 (Thr359/Ser363). It can be used for WB,IP assays with tag free, in the background of Human, Mouse, Rat.

HY-P83190

	Torsin 1A Antibody (YA2935) TOR1a; DQ2; DYT1; TorsinA	WB, FC	Human
	Torsin 1A Antibody (YA2935) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA2935), targeting Torsin 1A, with a predicted molecular weight of 38 kDa (observed band size: 35 kDa). Torsin 1A Antibody (YA2935) can be used for WB, FC experiment in human background.

HY-P81962

	PTF1A Antibody (YA1707) Pancreas-specific transcription factor 1a; bHLH transcription factor p48; PTF1-p48	WB, IP	Human, Rat
	PTF1A Antibody (YA1707) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA1707), targeting PTF1A, with a predicted molecular weight of 35 kDa (observed band size: 48 kDa). PTF1A Antibody (YA1707) can be used for WB, IP experiment in human, rat background.

HY-P80886

	RSK1 p90 Antibody (YA676) RPS6KA1; MAPKAPK1a; RSK1; Ribosomal protein S6 kinase alpha-1; S6K-alpha-1; 90 kDa ribosomal protein S6 kinase 1; p90-RSK 1; p90RSK1; p90S6K; MAP kinase-activated protein kinase 1a; MAPK-activated protein kinase 1a; MAPKAP kinase 1a; MAPKAP	WB, IP	Human, Mouse, Monkey
	RSK1 p90 Antibody (YA676) is a non-conjugated and Mouse origined monoclonal antibody about 83 kDa, targeting to RSK1 p90 (6B9). It can be used for WB,IP assays with tag free, in the background of Human, Mouse, Monkey.

HY-P81282

	Ikaros Antibody (YA987) CLL associated antigen KW 6; DNA-binding protein Ikaros; hIk 1; hIk-1; Hs.54452; IK1; Ikaros (zinc finger protein); IKAROS; IKAROS family zinc finger 1 (Ikaros); Ikaros family zinc finger protein 1; Ikzf1; IKZF1_HUMAN; LYF1; Lymphoid transcription factor LyF-1; PRO0758; Zinc finger protein subfamily 1a 1 (Ikaros); zinc finger protein subfamily 1a 1; Zinc finger protein; subfamily 1a; member 1; ZNFN1a1.	WB, IP	Human
	Ikaros Antibody (YA987) is a mouse-derived non-conjugated IgG1 antibody (Clone NO.: YA987), targeting Ikaros, with a predicted molecular weight of 58 kDa (observed band size: 58 kDa). Ikaros Antibody (YA987) can be used for WB, IP experiment in human background.

HY-P81282A

	Ikaros Antibody (YA988) CLL associated antigen KW 6; DNA-binding protein Ikaros; hIk 1; hIk-1; Hs.54452; IK1; Ikaros (zinc finger protein); IKAROS; IKAROS family zinc finger 1 (Ikaros); Ikaros family zinc finger protein 1; Ikzf1; IKZF1_HUMAN; LYF1; Lymphoid transcription factor LyF-1; PRO0758; Zinc finger protein subfamily 1a 1 (Ikaros); zinc finger protein subfamily 1a 1; Zinc finger protein; subfamily 1a; member 1; ZNFN1a1.	IHC-P	Human
	Ikaros Antibody (YA988) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA988), targeting Ikaros. Ikaros Antibody (YA988) can be used for IHC-P experiment in human background.

HY-P83257

	CC2D1A Antibody (YA3002) Coiled coil and C2 domain containing 1a; FREUD 1; Freud 1/Aki1; MRT3	WB, ICC/IF, FC	Human, Mouse, Rat
	CC2D1A Antibody (YA3002) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA3002), targeting CC2D1A, with a predicted molecular weight of 104 kDa (observed band size: 130 kDa). CC2D1A Antibody (YA3002) can be used for WB, ICC/IF, FC experiment in human, mouse, rat background.

HY-P81959

	T Cell Leukemia/Lymphoma Protein 1A Antibody (YA1704) Anti TCL1a; P14 TCL1; T cell leukemia 1; TCL1; TCL1 PEN; Tcl1a	WB, IHC-P, ICC/IF, FC	Human
	T Cell Leukemia/Lymphoma Protein 1A Antibody (YA1704) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA1704), targeting T Cell Leukemia/Lymphoma Protein 1A, with a predicted molecular weight of 13 kDa (observed band size: 13 kDa). T Cell Leukemia/Lymphoma Protein 1A Antibody (YA1704) can be used for WB, IHC-P, ICC/IF, FC experiment in human background.

HY-P82254

	p60 CAF1 Antibody (YA1999) CAF 1a; CAF IP60; CAF-1; CAF1; CAF1a; CAF1P60; CHAF1B; MPHOSPH7; MPP7	WB, IHC-P, ICC/IF, IP, FC	Human
	p60 CAF1 Antibody (YA1999) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA1999), targeting p60 CAF1, with a predicted molecular weight of 61 kDa (observed band size: 70 kDa). p60 CAF1 Antibody (YA1999) can be used for WB, IHC-P, ICC/IF, IP, FC experiment in human background.

HY-P83364

	PPP1R1A Antibody (YA3109) I 1; I1; Inhibitor 1; IPP1; Ppp1r1a; Protein phosphatase 1 regulatory (inhibitor) subunit 1a	WB, IHC-P, ICC/IF, IP, FC	Human, Mouse, Rat
	PPP1R1A Antibody (YA3109) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA3109), targeting PPP1R1A, with a predicted molecular weight of 19 kDa (observed band size: 27 kDa). PPP1R1A Antibody (YA3109) can be used for WB, IHC-P, ICC/IF, IP, FC experiment in human, mouse, rat background.

HY-P82314

	alpha 1a Adrenergic Receptor Antibody (YA2059) ADRA1a; ADRA1C; Alpha-1a adrenergic receptor; Alpha-1a adrenoreceptor; Alpha-1a adrenoceptor; Alpha-1C adrenergic receptor; Alpha-adrenergic receptor 1c	WB, IHC-P	Rat
	alpha 1a Adrenergic Receptor Antibody (YA2059) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA2059), targeting alpha 1a Adrenergic Receptor, with a predicted molecular weight of 51 kDa (observed band size: 51 kDa). alpha 1a Adrenergic Receptor Antibody (YA2059) can be used for WB, IHC-P experiment in rat background.

HY-P80731

	KDM1A Antibody (YA718) KDM1a; AOF2; KDM1; KIAA0601; LSD1; Lysine-specific histone demethylase 1a; BRAF35-HDAC complex protein BHC110; Flavin-containing amine oxidase domain-containing protein 2	WB	Human, Mouse, Monkey
	KDM1A Antibody (YA718) is a non-conjugated and Mouse origined monoclonal antibody about 93 kDa, targeting to KDM1A (1B2). It can be used for WB assays with tag free, in the background of Human, Mouse, Monkey.

HY-P81167

	CPT1A Antibody CPT 1; CPT1a; CPTI-L; CPT1-L; carnitine palmitoyl transferase 1; Carnitine O-palmitoyltransferase 1, liver isoform; CPT I; Carnitine palmitoyltransferase 1a; carnitine O-palmitoyltransferase 1, liver isoform isoform 1; CPT1a_HUMAN.	WB, ELISA	Mouse
	CPT1A Antibody is an unconjugated, approximately 86 kDa, rabbit-derived, anti-CPT1A polyclonal antibody. CPT1A Antibody can be used for: WB, ELISA expriments in mouse, and predicted: human, rat background without labeling.

HY-P80894

	SMC1A Antibody (YA673) Chromosome segregation protein SmcB; DXS423E; KIAA0178; MGC138332; Sb1.8; Segregation of mitotic chromosomes 1; SMC protein 1a; SMC-1-alpha; SMC-1a; SMC1 (structural maintenance of chromosomes 1 yeast) like 1; SMC1; SMC1 structural maintenance of chromoso	WB, ICC/IF	Human
	SMC1A Antibody (YA673) is a non-conjugated and Mouse origined monoclonal antibody about 143 kDa, targeting to SMC1A (4C5). It can be used for WB,ICC/IF assays with tag free, in the background of Human.

HY-P81115

	IL-1 alpha Antibody interleukin-1 alpha; Hematopoietin 1; IL 1 alpha; IL1 alpha; IL 1; IL 1a; Il-1a; IL1; IL1a; IL1F1; ilia; Interleukin 1 alpha; Interleukin 1 alpha precursor; Interleukin1 alpha; Preinterleukin 1 alpha; Pro interleukin 1 alpha; Prointerleukin 1 alpha; IL1a_HUMAN.	WB, ELISA, IHC-P, IHC-F, FC, ICC/IF	Human, Mouse
	IL-1 alpha Antibody is a rabbit-derived non-conjugated IgG antibody, targeting IL-1 alpha, with a predicted molecular weight of 31 kDa. IL-1 alpha Antibody can be used for WB, ELISA, IHC-P, IHC-F, FC, ICC/IF experiments in human, mouse backgrounds.

HY-P80706

	Histone H2B Antibody (YA737) H2BK5ac; H2B 1a; H2B; H2B histone family; H2B2f; H2Ba; H2Bf; HIST2H2BF; histone H2B; histone H2B type 1; Histone H2B type 2-F	WB, IHC-P	Human, Mouse, Rat
	Histone H2B Antibody (YA737) is a non-conjugated and Mouse origined monoclonal antibody about 14 kDa, targeting to Histone H2B (7E2). It can be used for WB,IHC-P assays with tag free, in the background of Human, Mouse, Rat.

HY-P80728

	JNK Antibody AI849689; c Jun N terminal kinase 1; C-JUN kinase 1; c-Jun N-terminal kinase 1; EC 2.7.11.24; JAK 1a; JAK1a; JNK 1; JNK 46; JNK; JNK-46; JNK1a2; JNK21B1/2; MAP kinase 8; MAPK 8; MAPK8; Mitogen activated protein kinase 8; Mitogen-activated protein kinase 8	WB, IP	Human, Mouse, Rat, Hamster
	JNK Antibody is a non-conjugated and Rabbit origined monoclonal antibody about 48 kDa, targeting to JNK. It can be used for WB,IP assays with tag free, in the background of Human, Mouse, Rat, Hamster.

HY-P80729

	JNK1 Antibody (YA720) AI849689; c Jun N terminal kinase 1; C-JUN kinase 1; c-Jun N-terminal kinase 1; EC 2.7.11.24; JAK 1a; JAK1a; JNK 1; JNK 46; JNK; JNK-46; JNK1a2; JNK21B1/2; MAP kinase 8; MAPK 8; MAPK8; Mitogen activated protein kinase 8; Mitogen-activated protein kinase 8	WB, ICC/IF	Human, Mouse, Rat
	JNK1 (1A4) Antibody is a non-conjugated and Mouse origined monoclonal antibody about 48 kDa, targeting to JNK1 (1A4). It can be used for WB,ICC/IF assays with tag free, in the background of Human, Mouse, Rat.

HY-P80831

	Phospho-JNK1 (Thr183/Tyr185) Antibody AI849689; c Jun N terminal kinase 1; C-JUN kinase 1; c-Jun N-terminal kinase 1; EC 2.7.11.24; JAK 1a; JAK1a; JNK 1; JNK 46; JNK; JNK-46; JNK1a2; JNK21B1/2; MAP kinase 8; MAPK 8; MAPK8; Mitogen activated protein kinase 8; Mitogen-activated protein kinase 8	WB, IP	Human, Rat
	Phospho-JNK1 (Thr183/Tyr185) Antibody is a non-conjugated and Rabbit origined monoclonal antibody about 48 kDa, targeting to Phospho-JNK1 (Thr183/Tyr185). It can be used for WB,IP assays with tag free, in the background of Human, Rat.

HY-P82405

	MARK3 Antibody (YA2150) C-TAK1 antibody; Cdc25C associated protein kinase 1 antibody; Cdc25C-associated protein kinase 1 antibody; cTAK1 antibody; ELKL motif kinase 2 antibody; EMK-2 antibody; Emk2 antibody; ETK 1 antibody; KIAA4230 antibody; KP78 antibody; MAP microtubule affinity regulating kinase 3 antibody; MAP/microtubule affinity-regulating kinase 3 antibody; Mark3 antibody; MARK3_HUMAN antibody; Par 1a antibody; PAR1a antibody; Protein kinase STK10 antibody; Ser/Thr protein kinase PAR-1 antibody; Serine threonine protein kinase p78 antibody; Serine/threonine-protein kinase p78 antibody; SerThr protein kinase PAR 1 antibody	WB, ICC/IF, IP, FC	Mouse, Human
	MARK3 Antibody (YA2150) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA2150), targeting MARK3, with a predicted molecular weight of 84 kDa (observed band size: 84 kDa). MARK3 Antibody (YA2150) can be used for WB, ICC/IF, IP, FC experiment in mouse, human background.

HY-P82015

	U1A Antibody (YA1760) Mud1; snRNP A; SNRPA; U1-A; U1a	WB, ICC/IF, IP	Human, Mouse, Rat
	U1A Antibody (YA1760) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA1760), targeting U1A, with a predicted molecular weight of 31 kDa (observed band size: 31 kDa). U1A Antibody (YA1760) can be used for WB, ICC/IF, IP experiment in human, mouse, rat background.

HY-P80654

	Elongation Factor 1A1 Antibody EEF1a1; CCS-3; CCS3; EEF-1; EEF1a; EF-Tu; EF1a; GRAF-1EF; LENG7; PTI1; eEF1a-1	WB, IHC-P, IP	Human, Mouse, Rat
	Elongation Factor 1A1 Antibody is a non-conjugated and Rabbit origined monoclonal antibody about 50 kDa, targeting to Elongation Factor 1A1. It can be used for WB,IHC-P,IP assays with tag free, in the background of Human, Mouse, Rat.

HY-P80132

	FOXO1A Antibody	WB, ICC/IF, IHC-P	Human, Mouse
	FOXO1A Antibody is a non-conjugated and Rabbit origined monoclonal antibody about 70 kDa, targeting to FOXO1A. It can be used for WB,ICC,IHC-P assays with tag free, in the background of Human, Mouse.

HY-P80649

	eIF1A Antibody EIF1a; EIF4C; eIF-1a; eIF-4C; EIF1aP1	WB, IHC-F, IHC-P, ICC/IF, IP	Human, Mouse, Rat
	eIF1A Antibody is a non-conjugated and Rabbit origined monoclonal antibody about 16 kDa, targeting to eIF1A. It can be used for WB,IHC-F,IHC-P,ICC/IF,IP assays with tag free, in the background of Human, Mouse, Rat.

HY-P83634

	CD1a Antibody (YA3379) CD1a; T-cell surface glycoprotein CD1a; T-cell surface antigen T6/Leu-6; hTa1 thymocyte antigen; CD antigen CD1a	WB, IHC-P	Human
	CD1a Antibody (YA3379) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA3379), targeting CD1a, with a predicted molecular weight of 37 kDa (observed band size: 37 kDa). CD1a Antibody (YA3379) can be used for WB, IHC-P experiment in human background.

HY-P82606

	RING1 Antibody (YA2351) Ring1a; Ring1; RING1a; Rnf1	WB, IHC-P, ICC/IF	Human
	RING1 Antibody (YA2351) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA2351), targeting RING1, with a predicted molecular weight of 42 kDa (observed band size: 50 kDa). RING1 Antibody (YA2351) can be used for WB, IHC-P, ICC/IF experiment in human background.

HY-P82741

	Carboxypeptidase A1/A2/B Antibody (YA2486) Carboxypeptidase A1+A2+B	WB, IHC-P, ICC/IF	Human, Mouse, Rat
	Carboxypeptidase A1/A2/B Antibody (YA2486) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA2486), targeting Carboxypeptidase A1/A2/B, with a predicted molecular weight of 47 kDa (observed band size: 44 kDa). Carboxypeptidase A1/A2/B Antibody (YA2486) can be used for WB, IHC-P, ICC/IF experiment in human, mouse, rat background.

HY-P83454

	MAT1A Antibody (YA3199) MAT; SAMS; MATA1; SAMS1; MAT1a	WB, IP	Human, Mouse, Rat
	MAT1A Antibody (YA3199) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA3199), targeting MAT1A, with a predicted molecular weight of 44 kDa (observed band size: 44 kDa). MAT1A Antibody (YA3199) can be used for WB, IP experiment in human, mouse, rat background.

HY-P82717

	ATP1A3 Antibody (YA2462) AHC2; Atp1a3; DYT12; RDP	WB	Human, Mouse, Rat
	ATP1A3 Antibody (YA2462) is a biotin-conjugated non-conjugated IgG antibody, targeting ATP1A3, with a predicted molecular weight of 112 kDa (observed band size: 100-150 kDa). ATP1A3 Antibody (YA2462) can be used for WB experiment in human, mouse, rat background.

HY-P81923

	FHL1 Antibody (YA1668) FHL1; FHL1a; FHL1B; FLH1a; RBMX1a; RBMX1B; SLIM1; SLIMMER; XMPMA	WB, IHC-P, IP	Human, Mouse, Rat
	FHL1 Antibody (YA1668) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA1668), targeting FHL1, with a predicted molecular weight of 36 kDa (observed band size: 30 kDa). FHL1 Antibody (YA1668) can be used for WB, IHC-P, IP experiment in human, mouse, rat background.

HY-P83189

	ATP1A2 Antibody (YA2934) Atp1a2; FHM2; KIAA0778; MHP2	WB	Human, Mouse, Rat
	ATP1A2 Antibody (YA2934) is a biotin-conjugated non-conjugated IgG antibody, targeting ATP1A2, with a predicted molecular weight of 112 kDa (observed band size: 102 kDa). ATP1A2 Antibody (YA2934) can be used for WB experiment in human, mouse, rat background.

HY-P80537

	ATP1A1 Antibody A1a1; AT1a1; ATP1a1; Na+/K+ transporting; alpha 1 polypeptide; Na+/K+ ATPase 1; Na; K-ATPase 1; Sodium pump 1	WB, IHC-P, ICC/IF, FC	Human, Mouse, Rat
	alpha 1 Sodium Potassium ATPase Antibody is a non-conjugated and Rabbit origined polyclonal antibody about 113 kDa, targeting to alpha 1 Sodium Potassium ATPase. It can be used for WB,IHC-P,ICC/IF,FC assays with tag free, in the background of Human, Mouse, Rat.

HY-P82830

	NCF1 Antibody (YA2575) NCF1; NCF1a; NOXO2; SH3PXD1a; p47phox	WB, IP	Human
	NCF1 Antibody (YA2575) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA2575), targeting NCF1, with a predicted molecular weight of 45 kDa (observed band size: 45 kDa). NCF1 Antibody (YA2575) can be used for WB, IP experiment in human background.

HY-P82528

	TRIM24 Antibody (YA2273) PTC6; TF1a; TIF1; RNF82; TIF1a; hTIF1; TIF1aLPHA	WB	Human
	TRIM24 Antibody (YA2273) is a biotin-conjugated non-conjugated IgG antibody, targeting TRIM24, with a predicted molecular weight of 117 kDa (observed band size: 117 kDa). TRIM24 Antibody (YA2273) can be used for WB experiment in human background.

HY-P82632

	Estrogen Inducible Protein pS2 Antibody (YA2377) hP1.A; HP1a; HPS2; pNR2; pS2; TFF1	WB, IHC-P, ICC/IF, IP, FC	Human
	Estrogen Inducible Protein pS2 Antibody (YA2377) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA2377), targeting Estrogen Inducible Protein pS2, with a predicted molecular weight of 9 kDa (observed band size: 9 kDa). Estrogen Inducible Protein pS2 Antibody (YA2377) can be used for WB, IHC-P, ICC/IF, IP, FC experiment in human background.

HY-P81074

	FOXO1 Antibody FOXO1; FKHR; FOXO1a; Forkhead box protein O1; Forkhead box protein O1a; Forkhead in rhabdomyosarcoma	WB, IHC-F, IHC-P, ICC/IF, ELISA, ChIP	Human, Mouse, Rat, Pig
	FOXO1 Antibody is a rabbit-derived non-conjugated IgG antibody, targeting FOXO1, with a predicted molecular weight of 78 kDa . FOXO1 Antibody can be used for WB, IHC-F, IHC-P, ICC/IF, ELISA, ChIP experiments in human, mouse, rat, pig backgrounds.

HY-P82768

	OR1A1 Antibody (YA2513) OR17-7	WB, IP	Human, Mouse, Rat
	OR1A1 Antibody (YA2513) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA2513), targeting OR1A1, with a predicted molecular weight of 35 kDa (observed band size: 35 kDa). OR1A1 Antibody (YA2513) can be used for WB, IP experiment in human, mouse, rat background.

HY-P83096

	FNTA Antibody (YA2841) FPTA; PTAR2; PGGT1a	WB, IHC-F, IHC-P, ICC/IF	Human, Rat
	FNTA Antibody (YA2841) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA2841), targeting FNTA, with a predicted molecular weight of 44 kDa (observed band size: 44 kDa). FNTA Antibody (YA2841) can be used for WB, IHC-F, IHC-P, ICC/IF experiment in human, rat background.

HY-P83192

	Guanylyl Cyclase alpha 1 Antibody (YA2937) GUCY1a3; GC-S-alpha-1; GUC1a3; GUCA3; GCS-alpha-3; GUCY1a1; GC-SA3; GCS-alpha-1; GUCSA3	WB	Human
	Guanylyl Cyclase alpha 1 Antibody (YA2937) is a biotin-conjugated non-conjugated IgG antibody, targeting Guanylyl Cyclase alpha 1, with a predicted molecular weight of 77 kDa (observed band size: 73 kDa). Guanylyl Cyclase alpha 1 Antibody (YA2937) can be used for WB experiment in human background.

HY-P80676

	FOXO1 Antibody (YA430) FOXO1; FKHR; FOXO1a; Forkhead box protein O1; Forkhead box protein O1a; Forkhead in rhabdomyosarcoma	WB, IHC-F, IHC-P, ICC/IF	Human
	FOXO1 Antibody is a non-conjugated and Rabbit origined monoclonal antibody about 70 kDa, targeting to FOXO1. It can be used for WB,IHC-F,IHC-P,ICC/IF assays with tag free, in the background of Human.

HY-P83214

	HCE Antibody (YA2959) HCE; HCE1; hCAP; CAP1a	WB, ICC/IF, IP	Human, Rat
	HCE Antibody (YA2959) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA2959), targeting HCE, with a predicted molecular weight of 69 kDa (observed band size: 69 kDa). HCE Antibody (YA2959) can be used for WB, ICC/IF, IP experiment in human, rat background.

HY-P82205

	SH2D1A Antibody (YA1950) LYP; SAP; XLP; DSHP; EBVS; IMD5; XLPD; MTCP1; XLPD1; SAP/SH2D1a	WB	Human, Mouse, Rat
	SH2D1A Antibody (YA1950) is a biotin-conjugated non-conjugated IgG antibody, targeting SH2D1A, with a predicted molecular weight of 14 kDa (observed band size: 14 kDa). SH2D1A Antibody (YA1950) can be used for WB experiment in human, mouse, rat background.

HY-P83134

	Elongation Factor 1A2 Antibody (YA2879) HS1; STN; EF1a; STNL; MRD38; EEF1aL; EIEE33; EF-1-alpha-2	WB, IP	Human, Mouse, Rat
	Elongation Factor 1A2 Antibody (YA2879) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA2879), targeting Elongation Factor 1A2, with a predicted molecular weight of 50 kDa (observed band size: 50 kDa). Elongation Factor 1A2 Antibody (YA2879) can be used for WB, IP experiment in human, mouse, rat background.

HY-P83135

	RNF20 Antibody (YA2880) BRE1-A; hBRE1; RING finger protein 20; E3 ubiquitin-protein ligase BRE1a; RNF20	WB, ICC/IF, IP, FC	Human, Mouse
	RNF20 Antibody (YA2880) is a rabbit-derived non-conjugated IgG antibody (Clone NO.: YA2880), targeting RNF20, with a predicted molecular weight of 114 kDa (observed band size: 114 kDa). RNF20 Antibody (YA2880) can be used for WB, ICC/IF, IP, FC experiment in human, mouse background.

HY-P83525

	Dopamine Receptor D1 Antibody (YA3270) D(1a) dopamine receptor; DADR; Dopamine D1 receptor; DR D1al; DRD1; DRD1a	WB	Human, Mouse, Rat
	Dopamine Receptor D1 Antibody (YA3270) is a biotin-conjugated non-conjugated IgG antibody, targeting Dopamine Receptor D1, with a predicted molecular weight of 49 kDa (observed band size: 75 kDa). Dopamine Receptor D1 Antibody (YA3270) can be used for WB experiment in human, mouse, rat background.

HY-P80878

	Pyruvate Dehydrogenase E1 alpha Antibody (YA681) mitochondrial; ODPA_HUMAN; PDH; PDHA; PDHA1; PDHCE1a; PDHE1 A type I; PDHE1-A type I; PHE1a; Pyruvate Dehydrogenase (lipoamide) alpha 1; Pyruvate dehydrogenase complex; E1 alpha polypeptide 1; Pyruvate Dehydrogenase E1 alpha; Pyruvate dehydrogenase E1 com	WB, ICC/IF	Human, Mouse
	Pyruvate Dehydrogenase E1 alpha Antibody (YA681) is a non-conjugated and Mouse origined monoclonal antibody about 43 kDa, targeting to Pyruvate Dehydrogenase E1 alpha (3H2). It can be used for WB,ICC/IF assays with tag free, in the background of Human, Mouse.

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