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STAP2 encodes the substrate of breast tumor kinase, an Src-type non-receptor tyrosine kinase. Zusätzlich bieten wir Ihnen Signal Transducing Adaptor Family Member 2 Antikörper (98) und viele weitere Produktgruppen zu diesem Protein an.
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These findings indicate an essential role for STAP2 in the generation of a high-quality memory CD8 (zeige CD8A Proteine)+ CTLs periphery, and suggest the therapeutic potential of STAP2 in cancer patients.
High STAP2 expression is associated with prostate cancer.
The Pyk2 (zeige PTK2B Proteine)/STAP-2 interaction is a novel mechanism to regulate SDF-1alpha-dependent T-cell chemotaxis.
STAP2 is upregulated in uterosacral ligaments in pelvic organ prolapse
Our results demonstrate a critical contribution of STAP-2 in BCR-ABL (zeige ABL1 Proteine) activity.
STAP-2 is a novel participant in the regulation of T cell apoptosis after stimulation
Interactions of STAP-2 with Brk (zeige PTK6 Proteine) and STAT3 (zeige STAT3 Proteine) participate in cell growth of human breast cancer cells.
STAP-2 expression in Jurkat T cells affects migration following stromal cell-derived factor-1alpha (SDF-1alpha) treatment; STAP-2 association with Vav1, the guanine-nucleotide exchanging factor for Rac1, enhances downstream Vav1/Rac1 signaling.
These data indicate that STAP-2/BKS negatively controls the FcepsilonRI (zeige FCER1G Proteine)-mediated calcium mobilization and degranulation by direct modulation of tyrosine phosphorylation of PLC (zeige HSPG2 Proteine)-gamma.
STAP-2/BKS is a modulator of STAT5 (zeige STAT5A Proteine)-mediated signaling
results demonstrate a contribution of CCR7 (zeige CCR7 Proteine) to STAP-2-dependent enhancement of BCR-ABL (zeige ABL1 Proteine)-mediated cell growth in Ba/F3 cells
signal transducing adaptor protein 2 (STAP-2) is involved in cell migration, proliferation, and melanogenesis as well as chemokine receptor expression and tumorigenesis in B16F10 melanoma cells
STAP-2 has a potential to regulate plural molecular events during pathological inflammatory responses.
Signal-transducing adaptor protein-2 controls the IgE-mediated, mast cell-mediated anaphylactic responses.
STAP-2 directly binds to c-Fms (zeige CSF1R Proteine) and interferes with the PI3K signaling, which leads to macrophage motility, in Raw 264.7 cells
STAP-2 associates with FAK (zeige PTK2 Proteine) and enhances its degradation, proteasome inhibitors block FAK (zeige PTK2 Proteine) degradation, and STAP-2 recruits an endogenous E3 ubiquitin ligase (zeige MUL1 Proteine), Cbl (zeige CBL Proteine), to FAK (zeige PTK2 Proteine).
This gene encodes the substrate of breast tumor kinase, an Src-type non-receptor tyrosine kinase. The encoded protein possesses domains and several tyrosine phosphorylation sites characteristic of adaptor proteins that mediate the interactions linking proteins involved in signal transduction pathways. Alternative splicing results in multiple transcript variants.
signal-transducing adaptor protein 2
, BRK substrate
, breast tumor kinase substrate
, brk kinase substrate
, signal-transducing adaptor protein-2