货品编号: bioss.bsm-33319M
品牌: bioss
品名: Mouse Anti-PTEN antibody
规格: 50ul
产品描述:
Potential tumor suppressor. Acts as a phosphoinositide3-phosphatase by regulating PtdIns (3,4,5)P3 levels. Involved in
regulation of the AKT1 signaling pathway. The unphosphorylated form cooperates with AIP1 to suppress AKT1 activation.
The PTEN/MMAC1 discovers the first to have the suppress of the phosphoric acid enzyme activity cancer gene currently.
The gene of PTEN locates the chromosome10q23 area, sending forth sex tumor and a few households cancers with the
variety to suffer from the comprehensive disease easilyrelevant.The activity that passes to repress the Akt regulates the
cell period, the cell ground rule decease and glues to connect.This text discussed PTEN structure, function and its
correlationses, the PTEN is in tumor repress function mechanism.
Function:
Tumor suppressor. Acts as a dual-specificity protein phosphatase, dephosphorylating tyrosine-, serine- and threonine-
phosphorylated proteins. Also acts as a lipid phosphatase, removing the phosphate in the D3 position of the inositol ring
from phosphatidylinositol 3,4,5-trisphosphate, phosphatidylinositol 3,4-diphosphate, phosphatidylinositol 3-phosphate and
inositol 1,3,4,5-tetrakisphosphate with order of substrate preference in vitro PtdIns(3,4,5)P3 > PtdIns(3,4)P2 > PtdIns3P >
Ins(1,3,4,5)P4. The lipid phosphatase activity is critical for its tumor suppressor function. Antagonizes the PI3K-AKT/PKB
signaling pathway by dephosphorylating phosphoinositides and thereby modulating cell cycle progression and cell survival.
The unphosphorylated form cooperates with AIP1 to suppress AKT1 activation. Dephosphorylates tyrosine-phosphorylated
focal adhesion kinase and inhibits cell migration and integrin-mediated cell spreading and focal adhesion formation. Plays a
role as a key modulator of the AKT-mTOR signaling pathway controlling the tempo of the process of newborn neurons integration
during adult neurogenesis, including correct neuron positioning, dendritic development and synapse formation. May be a negative
regulator of insulin signaling and glucose
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