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The protein encoded by AGAP2 belongs to the centaurin gamma-like family. Additionally we are shipping ArfGAP with GTPase Domain, Ankyrin Repeat and PH Domain 2 Antibodies (103) and ArfGAP with GTPase Domain, Ankyrin Repeat and PH Domain 2 Proteins (3) and many more products for this protein.
these findings support that PIKE amplification or overexpression coordinately acts with CDK4 (show CDK4 ELISA Kits) to drive glioblastoma tumorigenesis.
Studies showed that overexpression or mutation of PIKE has been observed in a variety of tumors, promoting cancer cell growth, transformation and invasion through AKT signaling or other signaling pathways, such as focal adhesion kinase. [review]
Mutation of Fyn (show FYN ELISA Kits) phosphorylation sites on PIKE-A, depletion of Fyn (show FYN ELISA Kits), or pharmacological inhibition of Fyn (show FYN ELISA Kits) blunts the association between PIKE-A and AMPK (show PRKAA1 ELISA Kits), resulting in loss of its inhibitory effect on AMPK (show PRKAA1 ELISA Kits).
expression of PLC-gamma1 (show PLCG1 ELISA Kits) and PIKE positively correlated with the tumor differentiation of oral squamous cell carcinoma.
PIKE reduction rescued PI3K (show PIK3CA ELISA Kits)-dependent and -independent neuronal defects in fragile X (show FMR1 ELISA Kits) syndrome.
In this review the CENTG1 gene is amplified in a variety of human cancers which lead to the enhancement of tumor invasion.
AGAP2 plays a role in the signalling and recycling of beta2-adrenergic receptors.
Fyn (show FYN ELISA Kits) regulates the activity of the adipogenic transcription factor signal transducer and activator of transcription 5a (STAT5a (show STAT5A ELISA Kits)) through enhancing its interaction with the GTPase (show RACGAP1 ELISA Kits) phosphoinositide 3-kinase enhancer A (PIKE-A).
PIKE is highly expressed in human squamous cell carcinoma and has a critical role in EGF (show EGF ELISA Kits)-induced squamous cell carcinoma proliferation.
The presence of heterogeneous missense mutations of GGAP2 in prostate cancer was associated with aggressive clinical behavior.
Depletion of PIKE-A in C2C12 myotubes diminished the inhibitory activities of TNF-alpha (show TNF ELISA Kits) on mitochondrial respiration and lipid oxidation, whereas PIKE-A overexpression exacerbated these cellular responses.
PIKE plays pivotal roles to advance oligodendroglia development and myelinogenesis through Akt (show AKT1 ELISA Kits)/mTOR (show FRAP1 ELISA Kits) activation.
Results demonstrate that the integrity of PIKE signaling is essential for protecting the neurons from excitotoxicity-stimulated damage both in vitro and in vivo.
PIKE is a critical factor in controlling synaptic AMPA (show GRIA3 ELISA Kits) receptor insertion.
data established the critical role of PIKE in regulating neuronal survival and development by substantiating the PI3K/Akt (show AKT1 ELISA Kits) pathway.
PIKE-A is required for prolactin (show PRL ELISA Kits)-mediated STAT5a (show STAT5A ELISA Kits) activation in mammary gland development.
PIKE knockout mice show augmented lipid oxidation, which is accompanied by enhanced AMPK (show PRKAA1 ELISA Kits) phosphorylation in muscle and adipose tissue and is implicated in obesity and diabetes development.
PIKE-L acts as a downstream survival effector for netrin-1 (show NTN1 ELISA Kits) through UNC5B (show UNC5B ELISA Kits) in the nervous system
The protein encoded by this gene belongs to the centaurin gamma-like family. It mediates anti-apoptotic effects of nerve growth factor by activating nuclear phosphoinositide 3-kinase. It is overexpressed in cancer cells, and promotes cancer cell invasion. Alternatively spliced transcript variants encoding different isoforms have been described for this gene.
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 2
, Arf GAP with GTP-binding protein-like, ANK repeat and PH domains 2
, GTP-binding and GTPase activating protein 2
, centaurin, gamma 1
, phosphatidylinositol 3-kinase enhancer
, phosphatidylinositol-3-kinase enhancer
, phosphoinositide 3-kinase enhancer
, nuclear GTPase PIKE