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Results for "

bioconjugates

" in MedChemExpress (MCE) Product Catalog:

12

Inhibitors & Agonists

1

Screening Libraries

4

Fluorescent Dye

1

Biochemical Assay Reagents

1

Click Chemistry

1

Oligonucleotides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-134566

    Fluorescent Dye Others
    NBD-X, SE, the acceptor fluorophore, can be used to create environment sensitive bioconjugates .
    NBD-X, SE
  • HY-W105411

    Biochemical Assay Reagents Others
    N,N'-Diacryloylpiperazine can be used to synthesize bioconjugates and other compounds, and can also be used in the fields of medicine and biotechnology. N,N'-Diacryloylpiperazine is a biomaterial or organic compound that can be used for life science research .
    N,N'-Diacryloylpiperazine
  • HY-135140A

    Others Others
    Methyltetrazine-Amine, a tetrazine compound, is used for the site-specific dual functionalization of the resulting bioconjugates .
    Methyltetrazine-amine hydrochloride
  • HY-15943
    6-TAMRA
    1 Publications Verification

    6-Carboxytetramethylrhodamine

    DNA Stain Others
    6-TAMRA has been a widely used fluorophore for preparing bioconjugates, especially fluorescent antibody and avidin derivatives used in immunochemistry.
    6-TAMRA
  • HY-149744

    Others Inflammation/Immunology
    FXb is an immunizing and functionalized hapten and can be used for protein bioconjugates preparation .
    FXb
  • HY-W040291

    Fluorescent Dye Cancer
    7-Hydroxy-4-methylcoumarin-3-acetic acid, SE is a blue fluorophore that has pH-dependent and environment-sensitive fluorescence. It is widely used for preparing bioconjugates of blue fluorescence.
    7-Hydroxy-4-methylcoumarin-3-acetic acid, SE
  • HY-164084

    Biochemical Assay Reagents Others
    DBCO-NHCO-C5-O-phenylethenesulfonyl fluoride is a DBCO containing linker, which can be used in bioconjugate, drug delivery and other biochemical research .
    DBCO-NHCO-C5-O-phenylethenesulfonyl fluoride
  • HY-155466

    Dopamine Receptor Neurological Disease
    Boc-MIF-1-Am (compound 2) is a human dopamine D2 receptor enhancer (EC50=17.82 nM) and is a bioconjugate of melanostatin (MIF-1) and amantadine. Boc-MIF-1-Am (200 μM) exhibited mild neurotoxicity in SH-SY5Y cells .
    Boc-MIF-1-Am
  • HY-160045

    Cholecystokinin Receptor Cancer
    AP1153 aptamer sodium is a DNA aptamer that specifically binds to the cholecystokinin receptor CCKBR (Kd: ~15 pM), but does not activate CCKBR-related signaling pathways. AP1153 aptamer sodium is internalized by pancreatic ductal adenocarcinoma (PDAC) cells in a receptor-mediated manner. AP1153 aptamer sodium can bioconjugate to the surface of fluorescent nanoparticles to facilitate nanoparticle delivery to PDAC tumors in vivo .
    AP1153 aptamer sodium
  • HY-D2165

    Fluorescent Dye Others
    AF 594 streptavidin is a bioconjugating agent. It consists of AF 594 and streptomycin, a streptomycin derivative of the red fluorescent dye AF 594. AF 594 has high fluorescence quantum yield and high photostability (Ex=594 nm, Em=615 nm). AF 594 streptavidin can be selectively conjugated to streptavidin-modified molecules via a streptomycin-modifying group for fluorescent labeling and spectroscopic analysis .
    AF 594 streptavidin
  • HY-161177

    PROTACs Ras Infection
    PROTAC KRAS G12D degrades SARS-CoV-2, 3-curd trypsin-like protease (3CLPro). Protac KRAS G12D degrades SARS-CoV-2, 3-curd trypsin-like protease (3CLPRO). The PROTAC molecule is designed by partially coupling a GC-376-based dipeptidyl 3CLPro ligand with pomadomide via a piperazine-piperidine linker .
    PROTAC KRAS G12D degrader 2
  • HY-125372

    ABAO

    Biochemical Assay Reagents Others
    2-Amino benzamidoxime (ABAO compound 6) can react quickly with aldehydes to form stable 1, 2-dihydroquinazoline 3-oxides in aqueous solutions. The 2-Amino benzamidoxime reaction process consists of the formation of a Schiff base as a rate-determining step, followed by rapid intramolecular cyclization. The reaction rate is dependent on pH, indicating that protonated benzamidoxime is involved in the formation of Schiff bases as an internal generalized acid. Substituents on the aromatic ring can increase the alkalinity of the aromatic amine, thus speeding up the reaction. The reactive properties of 2-Amino benzamidoxime make it a potential platform for the development of new bioconjugated strategies, fluorescent probes, and post-translational diversification of genetic coding libraries .
    2-Amino benzamidoxime

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