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Molecular Probes™ Fluoresceinyl Glycine Amide (5-(Aminoacetamido)Fluorescein) Non-distribution product as customer accommodation.

Fluoresceinyl Glycine Amide (5-(Aminoacetamido)Fluorescein)

Manufacturer:  Molecular Probes™ A1363

Catalog No. A1363


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Description

Description

The primary aliphatic amine of 5-(aminoacetamido)fluorescein (fluoresceinyl glycine amide) can be reversibly coupled to aldehydes and ketones to form a Schiff base - which can be reduced to a stable amine derivative by sodium borohydride (NaBH4) or sodium cyanoborohydride (NaCNH3) to form new probes. Carboxylic acids of proteins and other water-soluble biopolymers can be coupled to this molecule in aqueous solution using water-soluble carbodiimides such as EDAC (E2247). The glycine may be the better amine probe for direct carbodiimide-mediated coupling, since it is likely to remain unprotonated at a lower pH than other aliphatic amines.
Specifications

Specifications

Fluoresceinyl Glycine Amide (5-(Aminoacetamido)Fluorescein), 10mg, Orange, Solid, C22H16N2O6 Molecular Formula, 404.38 Molecular Weight, FITC (Fluorescein) Label, Aldehyde, Carboxylic Acid, Ketone Chemical Reactivity, 515/491nm Excitation/Emission Wavelen
Orange
FITC (Fluorescein)
Room temperature
404.38kDa
515nm
Solid
Labeling chemistry, protein labeling and crosslinking
Fluoresceinyl Glycine Amide (5-(Aminoacetamido)Fluorescein)
10mg
491nm
HPLC, 98% at 254nm
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