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Recombinant Human Short transient receptor potential channel 6 (TRPC6), Truncated

ACP01388

Number
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Specifications


Cat.No ACP01388 Target NameTRPC6
FormLiquid or Lyophilized powderExpression SystemMammalian cell
Expression Range543-592aaMol Weight34.7 kDa
Protein LengthPartialPurityGreater than 85% as determined by SDS-PAGE.
Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDQ9Y210
Background Information
  • Uniprot Id

    Q9Y210

  • Target Species

    Human

  • Target Name

    TRPC6

  • Target Full Name

    Short transient receptor potential channel 6

  • Target Function

    Thought to form a receptor-activated non-selective calcium permeant cation channel. Probably is operated by a phosphatidylinositol second messenger system activated by receptor tyrosine kinases or G-protein coupled receptors. Activated by diacylglycerol (DAG) in a membrane-delimited fashion, independently of protein kinase C. Seems not to be activated by intracellular calcium store depletion.

  • Target Involvement

    Focal segmental glomerulosclerosis 2 (FSGS2)

  • Target Subcellular Location

    Cell membrane; Multi-pass membrane protein.

  • Target Protein Families

    Transient receptor (TC 1.A.4) family, STrpC subfamily, TRPC6 sub-subfamily

  • Target Tissue Specificity

    Expressed primarily in placenta, lung, spleen, ovary and small intestine. Expressed in podocytes and is a component of the glomerular slit diaphragm.

  • Target Research Area

    Neuroscience

  • Target Synonyms

    TRP6; FSGS2; TRPC6

  • Target 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).

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