V900403
Gly-Gly
99%, Vetec™
Sinonimo/i:
Diglicina, Glicil-glicina
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About This Item
Formula condensata:
NH2CH2CONHCH2COOH
Numero CAS:
Peso molecolare:
132.12
Beilstein:
1765223
Numero CE:
Numero MDL:
Codice UNSPSC:
12352209
ID PubChem:
Prezzi e disponibilità al momento non sono disponibili
Prodotti consigliati
Nome del prodotto
Gly-Gly, Vetec™, reagent grade, 99%
Grado
reagent grade
Nome Commerciale
Vetec™
Saggio
99%
Stato
powder
tecniche
ligand binding assay: suitable
Colore
white
Intervallo di pH utile
7.5-8.9
pKa (25 °C)
8.2
Punto di fusione
255-260 °C
Stringa SMILE
NCC(=O)NCC(O)=O
InChI
1S/C4H8N2O3/c5-1-3(7)6-2-4(8)9/h1-2,5H2,(H,6,7)(H,8,9)
YMAWOPBAYDPSLA-UHFFFAOYSA-N
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Note legali
Vetec is a trademark of Merck KGaA, Darmstadt, Germany
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
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A Chatterjee et al.
Langmuir : the ACS journal of surfaces and colloids, 28(34), 12502-12508 (2012-08-21)
The early adsorption stage of glycylglycine on Si(111)7×7 surface has been studied by scanning tunneling microscopy (STM). Filled-state imaging shows that glycylglycine adsorbs dissociatively in a bidentate fashion on two adjacent Si adatoms across a dimer wall or an adatom-restatom
Lasse Jenner et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(10), 3812-3816 (2013-02-23)
Here we present an X-ray crystallography structure of the clinically relevant tigecycline antibiotic bound to the 70S ribosome. Our structural and biochemical analysis indicate that the enhanced potency of tigecycline results from a stacking interaction with nucleobase C1054 within the
Francis Impens et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(34), 12432-12437 (2014-08-13)
SUMOylation is an essential ubiquitin-like modification involved in important biological processes in eukaryotic cells. Identification of small ubiquitin-related modifier (SUMO)-conjugated residues in proteins is critical for understanding the role of SUMOylation but remains experimentally challenging. We have set up a
Eduard Schreiner et al.
Journal of the American Chemical Society, 133(21), 8216-8226 (2011-05-13)
A comprehensive study of free energy landscapes and mechanisms of COS-mediated polymerization of glycine via N-carboxy anhydrides (NCAs, "Leuchs anhydrides") and peptide hydrolysis at the water-pyrite interface at extreme thermodynamic conditions is presented. Particular emphasis is set on the catalytic
Namrata D Udeshi et al.
Molecular & cellular proteomics : MCP, 12(3), 825-831 (2012-12-26)
Detection of endogenous ubiquitination sites by mass spectrometry has dramatically improved with the commercialization of anti-di-glycine remnant (K-ε-GG) antibodies. Here, we describe a number of improvements to the K-ε-GG enrichment workflow, including optimized antibody and peptide input requirements, antibody cross-linking
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