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Results for "

BDP TR amine

" in MedChemExpress (MCE) Product Catalog:

By Targets:	Fluorescent Dye (2)

Inhibitors & Agonists

Fluorescent Dye

Targets Recommended: Trace Amine-associated Receptor (TAAR) VAP-1

Cat. No.	Product Name	Target	Research Areas	Chemical Structure

HY-D1371

BDP TR amine hydrochloride	Fluorescent Dye
BDP TR amine hydrochlorideis one of a class of boron diindolyl methylene (BDI) dyes suitable for TAMRA channels. Commonly used for oligonucleotide labeling and amino acid sequencing.

HY-W414380

Bdp tr nhs ester	Fluorescent Dye	Others
Bdp tr nhs ester is a chemiluminescent coupling compound with a long excited state lifetime for immunoassays and is suitable for microscopy and fluorescence polarization analysis applications. NHS ester can react specifically and efficiently with the side chains of primary amines such as lysine residues or amino silane coated surfaces under neutral or weakly basic conditions to form covalent bonds .

Cat. No.	Product Name	Type

HY-D1371

BDP TR amine hydrochloride	Dyes
BDP TR amine hydrochlorideis one of a class of boron diindolyl methylene (BDI) dyes suitable for TAMRA channels. Commonly used for oligonucleotide labeling and amino acid sequencing.

HY-W414380

Bdp tr nhs ester	Fluorescent Dyes/Probes
Bdp tr nhs ester is a chemiluminescent coupling compound with a long excited state lifetime for immunoassays and is suitable for microscopy and fluorescence polarization analysis applications. NHS ester can react specifically and efficiently with the side chains of primary amines such as lysine residues or amino silane coated surfaces under neutral or weakly basic conditions to form covalent bonds .

Bdp tr nhs ester

Fluorescent Dyes/Probes

Bdp tr nhs ester is a chemiluminescent coupling compound with a long excited state lifetime for immunoassays and is suitable for microscopy and fluorescence polarization analysis applications. NHS ester can react specifically and efficiently with the side chains of primary amines such as lysine residues or amino silane coated surfaces under neutral or weakly basic conditions to form covalent bonds .

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