Chemodex

(+)-Biotin N-hydroxysuccinimide ester

CHF 66.00
In stock
CDX-B0145-M100100 mgCHF 66.00
CDX-B0145-M250250 mgCHF 150.00
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Product Details
Synonyms (+)-Biotin N-succinimidyl ester; d-Biotin NHS ester; BNHS; Biotinyl-N-hydroxy-succinimide; N-Hydroxysuccinimidobiotin; N-Succinimidyl D-biotinate; NHS-Biotin; Biotin-Osu; NSC 345668
Product Type Chemical
Properties
Formula

C14H19N3O5S

MW 341.38
CAS 35013-72-0
Source/Host Chemicals Synthetic.
Purity Chemicals ≥98% (HPLC)
Appearance White to off-white powder.
Solubility Soluble in DMSO or DMF.
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key YMXHPSHLTSZXKH-RVBZMBCESA-N
Smiles O=C(ON1C(CCC1=O)=O)CCCC[C@@H]2SC[C@@]3([H])[C@]2([H])NC(N3)=O
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description

Biotin succinimidyl ester is the most popular amine-reactive biotinylating agent for modifying proteins, peptides, antibodies, oligonucleotides, microbeads and other biological molecules. It forms irreversible amide bonds. Typically coupled to primary amine in the pH range 6.5-8.5. This cell-permable activated biotin derivative can be readily coupled to primary or secondary amines of analyte compounds or proteins under mild conditions. The resulting biotinylated derivatives have been widely used in streptavidin or avidin systems and labeling methods, with many applications in immunology and histochemistry. It is used to selectively label Escherichia coli cell envelope proteins in vivo. It preferentially labels outer membrane, periplasmic, and inner membrane proteins as well as a specific inner membrane marker protein (Tet-LacZ).

Product References

(1) D.M. Boorsma, et al.; J. Microsc. 143, 197 (1986) | (2) P. Kongtawelert & P. Ghosh; Clin. Chem. Acta 195, 17 (1990) | (3) G. Paganelli, et al.; Int. J. Cancer 45, 1184 (1990) | (4) C. Wagener, et al.; Meth. Enzymol. 184, 518 (1990) | (5) B. Baumeister, et al.; Int. J. Pep. Res. Therap. 11, 139 (2005) | (6) G.T. Hermanson; Bioconjugate Techn. 2nd p506-545 (2008)

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