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CSK Protein (GST tag)

Cette protéine Recombinant CSK est exprimée dans Baculovirus infected Insect Cells.
N° du produit ABIN7317088
746,00 €
Plus frais de livraison 40,00 € et TVA
50 μg
Destination: France
Envoi sous 9 à 13 jours ouvrables

Aperçu rapide pour CSK Protein (GST tag) (ABIN7317088)

Antigène

Voir toutes CSK Protéines
CSK (C-Src tyrosine Kinase (CSK))

Type de proteíne

Recombinant

Activité biologique

Active

Origine

  • 10
  • 3
  • 1
  • 1
  • 1
Humain

Source

  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
Baculovirus infected Insect Cells

Pureté

> 92 % as determined by reducing SDS-PAGE.
  • Purification/Conjugué

    Cette CSK protéine est marqué à la GST tag.

    Fonction

    Recombinant Human CSK/C-Src kinase Protein (GST Tag)(Active)

    Séquence

    Met 1-Leu 450

    Attributs du produit

    A DNA sequence encoding the human CSK (NP_004374.1) (Met 1-Leu 450) was fused with the GST tag at the N-terminus.

    niveau d'endotoxine

    < 1.0 EU per μg as determined by the LAL method.

    Biological Activity Comment

    The specific activity was determined to be 127 nmol/min/mg using Poly(Glu,Tyr) 4:1 as substrate.
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  • Restrictions

    For Research Use only
  • Format

    Frozen, Liquid

    Buffer

    Supplied as sterile 20 mM Tris, 500 mM NaCl, 0.5 mM PMSF, pH 7.4

    Stock

    -20 °C

    Stockage commentaire

    Store at < -20°C, stable for 6 months. Please minimize freeze-thaw cycles.
  • Antigène

    CSK (C-Src tyrosine Kinase (CSK))

    Autre désignation

    CSK/C-Src kinase

    Sujet

    Background: The tyrosine kinase c-Src has been implicated as a modulator of cell proliferation, spreading, and migration. These functions are also regulated by Met. The structure of a large fragment of the c-Src kinase comprises the regulatory and kinase domains and the carboxy-terminal tall. c-Src kinase interactions among domains and is stabilized by binding of the phosphorylated tail to the SH2 domain. This molecule is locked in a conformation that simultaneously disrupts the kinase active site and sequesters the binding surfaces of the SH2 and SH3 domains. The structure shows how appropriate cellular signals, or transforming mutations in v-Src, could break these interactions to produce an open, active kinase. The protein-tyrosine kinase activity of c-Src kinase is inhibited by phosphorylation of tyr527, within the c-Src c-terminal tail. Genetic and biochemical data have suggested that this negative regulation requires an intact Src homology 2 (SH2) domain. Since SH2 domains recognize phosphotyrosine, it is possible that these two non-catalytic domains associate, and thereby repress c-Src kinase activity. Experiments have suggested that c-Src kinase plays a role in the biological behaviour of colonic carcinoma cells induced by migratory factors such as EGF, perhaps acting in conjunction with FAK to regulate focal adhesion turnover and tumour cell motility. Furthermore, although c-Src kinase has been implicated in colonic tumour progression, in the adenoma to carcinoma in vitro model c-Src is not the driving force for this progression but co-operates with other molecules in carcinoma development. References

    Synonym: MGC117393,CSK

    Poids moléculaire

    77 kDa

    NCBI Accession

    NP_004374

    Pathways

    TCR Signaling, EGFR Signaling Pathway, Cell-Cell Junction Organization, CXCR4-mediated Signaling Events
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