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NISCH encodes a nonadrenergic imidazoline-1 receptor protein that localizes to the cytosol and anchors to the inner layer of the plasma membrane. Additionally we are shipping Nischarin Kits (6) and Nischarin Proteins (6) and many more products for this protein.
Showing 10 out of 19 products:
Human Monoclonal Nischarin Primary Antibody for IF, WB - ABIN967586
Alahari: Nischarin inhibits Rac induced migration and invasion of epithelial cells by affecting signaling cascades involving PAK. in Experimental cell research 2003
Show all 5 references for ABIN967586
Nischarin inhibits neurite outgrowth by blocking PAK1 (show PAK1 Antibodies) activation in neurons.
Data from studies using various receptor antagonists/agonists suggest that imidazoline receptors (Nisch I-1), alpha2-adrenoceptors, and endothelin-A receptors are involved in body temperature regulation in mice.
Data suggest that both IR1 and IR2 (imidazoline receptor 2) play roles in acquisition of behavioral responses in alcoholism; activation of IR1 and IR2 may serve as molecular targets in prevention (and possibly treatment) of alcoholism.
Activation of I-1 R may activate FXR (show NR1H4 Antibodies) to lower plasma lipids, suggesting I-1 R as a new target for the treatment of hyperlipidemia.
guanidine increases glucose uptake via an activation of imidazoline I2 receptor through AMPK (show PRKAA1 Antibodies) activation in skeletal muscle cell.
Nisch regulates cell movement by inhibiting PAK.
Data suggest that nischarin, in addition to regulating the p21-activated kinase (PAK) strand of Rac1 signaling, can also regulate other links in the web of Rac1 signaling pathways.
Nischarin may serve as the functional I1-receptor
Data found that NISCH was significantly downregulated in ovarian neoplasm through its promotor silencing with hypermethylation and its expression was correlated with poor prognosis.
Nischarin expression may therefore be used as a marker to predict the invasiveness and metastasis of primary breast cancer
Tobacco smoke induces methylation changes in the NISCH gene promoter before any detectable cancer.
unctional interaction between LKB1 (show STK11 Antibodies) and Nischarin to inhibit cell migration and breast tumor progression
Imidazoline receptor 1 gene plays a role in the development of cardiac hypertrophy and ventirular remodeling.
Nischarin reduces alpha5 integrin expression leading to reduction of FAK (show PTK2 Antibodies) phosphorylation and Rac (show AKT1 Antibodies) GTP (show AK3 Antibodies) loading, which in turn reduces tumor growth. NISCH also regulates PAK and LIMK (show LIMK1 Antibodies) signaling.
Insulin receptor substrate 4 (show IRS4 Antibodies) associates with the protein IRAS (IRAS protein)
I(1)-receptors can abrogate the primary signaling cascade activated by NGF (show NGFB Antibodies), most likely by increasing levels of a specific phosphatase to return dually phosphorylated ERK (show EPHB2 Antibodies) to its unphosphorylated state.
hIRAS expression in PC12 cells resulted in protection against apoptosis
Results suggest that IRAS may represent a previously unknown anti-apoptotic protein involved in the regulation of cell survival.
This gene encodes a nonadrenergic imidazoline-1 receptor protein that localizes to the cytosol and anchors to the inner layer of the plasma membrane. The orthologous mouse protein has been shown to influence cytoskeletal organization and cell migration by binding to alpha-5-beta-1 integrin. In humans, this protein has been shown to bind to the adapter insulin receptor substrate 4 (IRS4) to mediate translocation of alpha-5 integrin from the cell membrane to endosomes. Expression of this protein was reduced in human breast cancers while its overexpression reduced tumor growth and metastasis\; possibly by limiting the expression of alpha-5 integrin. In human cardiac tissue, this gene was found to affect cell growth and death while in neural tissue it affected neuronal growth and differentiation. Alternative splicing results in multiple transcript variants encoding differerent isoforms. Some isoforms lack the expected C-terminal domains of a functional imidazoline receptor.
, imidazoline receptor 1
, imidazoline receptor I-1-like protein
, imidazoline-1 receptor
, I-1 receptor candidate protein
, imidazoline receptor I-1
, I1R candidate protein
, imidazoline receptor antisera selected