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Merck
CN

ALD00031

Biotin-PEG4-TPG hydrate

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关于此项目

经验公式(希尔记法):
C29H42N6O9S
分子量:
650.74
PubChem Substance ID:
UNSPSC Code:
12352200
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reaction suitability

reagent type: cross-linking reagent

SMILES string

O=CC(C1=CC=C(N2C=C(COCCOCCOCCOCCNC(CCCC[C@@H]3C4C(NC(N4)=O)CS3)=O)N=N2)C=C1)=O.O

InChI

1S/C29H40N6O8S.H2O/c36-18-25(37)21-5-7-23(8-6-21)35-17-22(33-34-35)19-43-16-15-42-14-13-41-12-11-40-10-9-30-27(38)4-2-1-3-26-28-24(20-44-26)31-29(39)32-28;/h5-8,17-18,24,26,28H,1-4,9-16,19-20H2,(H,30,38)(H2,31,32,39);1H2/t24?,26-,28?;/m1./s1

InChI key

ISXVHRHXXBUQMK-JOOSLKMSSA-N

Application

This compound is for specifically labeling arginines with biotin. This reagent contains a phenylglyoxyl group that reacts specifically with the guanidinyl group of arginine. The PEG linker improves aqueous solubility. After attachment to arginine the biotin can be used for capture by streptavidin. See the associated publication by Thompson et al. for more details about the compound.


存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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分析证书(COA)

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Darren A Thompson et al.
Journal of peptide science : an official publication of the European Peptide Society, 22(5), 311-319 (2016-03-24)
A new class of arginine-specific bioconjugation reagents for protein labeling has been developed. This method utilizes a triazolyl-phenylglyoxal group on the probe molecule that reacts selectively with the guandinyl group of Arg residues in a protein or peptide. The reaction