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CSK Protein (GST tag)

Dieses Recombinant CSK-Protein wird in Baculovirus infected Insect Cells exprimiert.
Produktnummer ABIN7317088
746,00 €
Zzgl. Versandkosten 20,00 € und MwSt
50 μg
Lieferung nach: Deutschland
Lieferung in 9 bis 13 Werktagen

Kurzübersicht für CSK Protein (GST tag) (ABIN7317088)

Target

Alle CSK Proteine anzeigen
CSK (C-Src tyrosine Kinase (CSK))

Protein-Typ

Recombinant

Biologische Aktivität

Active

Spezies

  • 10
  • 3
  • 1
  • 1
  • 1
Human

Quelle

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

Reinheit

> 92 % as determined by reducing SDS-PAGE.
  • Aufreinigungstag / Konjugat

    Dieses CSK Protein ist gelabelt mit GST tag.

    Verwendungszweck

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

    Sequenz

    Met 1-Leu 450

    Produktmerkmale

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

    Endotoxin-Niveau

    < 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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  • Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Frozen, Liquid

    Buffer

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

    Lagerung

    -20 °C

    Informationen zur Lagerung

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

    CSK (C-Src tyrosine Kinase (CSK))

    Andere Bezeichnung

    CSK/C-Src kinase

    Hintergrund

    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

    Molekulargewicht

    77 kDa

    NCBI Accession

    NP_004374

    Pathways

    T-Zell Rezeptor Signalweg, EGFR Signaling Pathway, Cell-Cell Junction Organization, CXCR4-mediated Signaling Events
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