TRPC6 rabbit pAb
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TRPC6 rabbit pAb
Background :
The protein encoded by this gene forms a receptor-activated calcium channel in the cell membrane. The channel is activated by diacylglycerol and is thought to be under the control of a phosphatidylinositol second messenger system. Activation of this channel occurs independently of protein kinase C and is not triggered by low levels of intracellular calcium. Defects in this gene are a cause of focal segmental glomerulosclerosis 2 (FSGS2) . [provided by RefSeq, Mar 2009]Description :
The protein encoded by this gene forms a receptor-activated calcium channel in the cell membrane. The channel is activated by diacylglycerol and is thought to be under the control of a phosphatidylinositol second messenger system. Activation of this channel occurs independently of protein kinase C and is not triggered by low levels of intracellular calcium. Defects in this gene are a cause of focal segmental glomerulosclerosis 2 (FSGS2). [provided by RefSeq, Mar 2009],UniProt :
Q9Y210Swiss Prot :
Q9Y210Reactivity :
Human; MouseImmunogen :
Synthesized peptide derived from human TRPC6 AA range: 412-462Clonality :
PolyclonalSource :
RabbitApplications :
WBConcentration :
1 mg/mlDilution :
WB 1: 500-2000Storage Conditions :
-20°C/1 yearFragment :
IgGSubcellular Location :
Cell membrane ; Multi-pass membrane protein .Gene ID (Human) :
7225

