SCP0158
Granzyme B Substrate
≥95% (HPLC), lyophilized
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About This Item
Formule empirique (notation de Hill):
C32H41N5O11
Poids moléculaire :
671.69
Code UNSPSC :
12352204
Nomenclature NACRES :
NA.32
Produits recommandés
product name
Granzyme B Substrate,
Pureté
≥95% (HPLC)
Forme
lyophilized
Composition
Peptide Content, ≥85%
Conditions de stockage
protect from light
Température de stockage
−20°C
Amino Acid Sequence
Ac-Ile-Glu-Pro-Asp-AMC
Application
Granzyme B Substrate (Ac-IEPD-AMC) is a fluorogenic substrate for the detection and assay of caspase 8 and granzyme B which is involved in the rapid induction of target cell apoptosis by CTL in cell-mediated immune response.
Actions biochimiques/physiologiques
Granzymes belongs to serine proteinase family enzymes and it localizes along with perforin in granules. It is predominant in cytotoxic T cells. Granzyme B induces caspases dependent and independent cell death. It possesses specific cleavage action at aspartate residue in the substrate.
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Certificats d'analyse (COA)
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Fundamental Immunology, 1083-1083 (2008)
Kazimierz Weglarczyk et al.
Infection and immunity, 72(5), 2590-2597 (2004-04-23)
Human peripheral blood monocytes become apoptotic following phagocytosis and killing of Staphylococcus aureus. Although this type of monocyte apoptosis is known to be initiated by Fas-Fas ligand (FasL) interactions, the downstream signaling pathway has not been determined. In this work
Hideaki Toda et al.
Veterinary immunology and immunopathology, 141(1-2), 168-172 (2011-03-26)
Granzyme B plays an important role in granule-mediated apoptosis by CTL. It is a well characterized component of the cytolytic machinery in mammals and a candidate for the evaluation of cytotoxic activity of CTL as an alternative to conventional cytotoxicity
Basic Concepts of Molecular Pathology, 32-32 (2009)
M Hayashida et al.
Proceedings of the Society for Experimental Biology and Medicine. Society for Experimental Biology and Medicine (New York, N.Y.), 225(2), 143-150 (2000-10-24)
Cell death induction by cytotoxic T lymphocytes (CTLs) is an important thesis for the understanding of tumor immunotherapy. In the current study we investigated the molecular machinery of CTL-induced cell death in human hepatocellular carcinoma cell lines (HCC lines). CTLs
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