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G5136

Sigma-Aldrich

γ-Glu-ε-Lys

≥98.0% (TLC)

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About This Item

Empirische Formel (Hill-System):
C11H21N3O5
CAS-Nummer:
17105-15-6
Molekulargewicht:
275.30
MDL-Nummer:
MFCD00055787
UNSPSC-Code:
12352209
PubChem Substanz-ID:
24895198
NACRES:
NA.26

product name

γ-Glu-ε-Lys,

Assay

≥98.0% (TLC)

Qualitätsniveau

200

Form

powder

Farbe

white

Lagertemp.

−20°C

SMILES String

NC(CCCCNC(=O)CCC(N)C(O)=O)C(O)=O

InChI

1S/C11H21N3O5/c12-7(10(16)17)3-1-2-6-14-9(15)5-4-8(13)11(18)19/h7-8H,1-6,12-13H2,(H,14,15)(H,16,17)(H,18,19)

InChIKey

JPKNLFVGUZRHOB-UHFFFAOYSA-N

Anwendung

GammaGlu-epsilonLys (γ-Glu-ε-Lys) is used to study the functions and processing of endo-epsilon(-gamma-Glu)-Lys isopeptide bonds in biological processes.

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Transglutaminase aus Meerschweinchenleber lyophilized powder, ≥1.5 units/mg protein

Sigma-Aldrich

T5398

Transglutaminase aus Meerschweinchenleber

Pronase from Streptomyces griseus

Roche

PRON-RO

Pronase

Julian L Wong et al.
Development (Cambridge, England), 136(11), 1835-1847 (2009-05-01)
Fertilization is accompanied by the construction of an extracellular matrix that protects the new zygote. In sea urchins, this structure is built from glycoproteins residing at the egg surface and in secretory vesicles at the egg cortex. Four enzymatic activities
L Zavalova et al.
Molecular & general genetics : MGG, 253(1-2), 20-25 (1996-11-27)
We previously detected in salivary gland secretions of the medicinal leech (Hirudo medicinalis) a novel enzymatic activity, endo-epsilon(gamma-Glu)-Lys isopeptidase, which cleaves isopeptide bonds formed by transglutaminase (Factor XIIIa) between glutamine gamma-carboxamide and the epsilon-amino group of lysine. Such isopeptide bonds
Damien M O Halloran et al.
Tissue engineering, 12(6), 1467-1474 (2006-07-19)
This study investigated the effect on the mechanical and physicochemical properties of type II collagen scaffolds after cross-linking with microbial transglutaminase (mTGase). It is intended to develop a collagen-based scaffold to be used for the treatment of degenerated intervertebral discs.
I P Baskova et al.
Biochemistry. Biokhimiia, 66(12), 1368-1373 (2002-01-29)
Destabilase, endo-epsilon-(gamma-Glu)-Lys-isopeptidase, was prepared from the salivary gland secretion of the medicinal leech (Hirudo medicinalis). The secretion prepared by the known method of Rigbi et al. (1987) (secretion-K) lacks the destabilase-characteristic highly specific isopeptidase activity (the D-dimer-monomerizing activity) because of
Thomas M Jeitner et al.
Amino acids, 44(1), 129-142 (2012-03-13)
Transglutaminases catalyze the formation of γ-glutamylamines utilizing glutamyl residues and amine-bearing compounds such as lysyl residues and polyamines. These γ-glutamylamines can be released from proteins by proteases in an intact form. The free γ-glutamylamines can be catabolized to 5-oxo-L-proline and
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