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ATP2C1 polyclonal antibody

  • Catalog # : PAB19368
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  • Specification
  • Product Description:
  • Rabbit polyclonal antibody raised against synthetic peptide of ATP2C1.
  • Immunogen:
  • A synthetic peptide corresponding to 19 amino acids near C-terminus of human ATP2C1.
  • Host:
  • Rabbit
  • Reactivity:
  • Human, Mouse
  • Specificity:
  • At least four isoforms of ATP2C1 are known to exist; this antibody will recognize only the three longest isoforms. ATP2C1 antibody will not cross-react with ATP2C2.
  • Form:
  • Liquid
  • Purification:
  • Peptide affinity purification
  • Concentration:
  • 1 mg/mL
  • Recommend Usage:
  • Western Blot (1 ug/mL)
    Immunohistochemistry (5 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS (0.02% sodium azide)
  • Storage Instruction:
  • Store at 4°C for three months. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.
  • Note:
  • This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
  • Applications
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • Western blot analysis of ATP2C1 in mouse brain tissue lysate with ATP2C1 polyclonal antibody (Cat # PAB19368) at 1 ug/mL in (1) the absence and (2) the presence of blocking peptide.
  • Immunohistochemistry
  • Immunohistochemistry
  • Immunohistochemical staining of mouse brain cells with ATP2C1 polyclonal antibody (Cat # PAB19368) at 5 ug/mL.
  • ELISA
  • Application Image
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • enlarge
  • ELISA
  • Gene Information
  • Gene Name:
  • ATP2C1
  • Gene Alias:
  • ATP2C1A,BCPM,HHD,KIAA1347,PMR1,SPCA1,hSPCA1
  • Gene Description:
  • ATPase, Ca++ transporting, type 2C, member 1
  • Gene Summary:
  • The protein encoded by this gene belongs to the family of P-type cation transport ATPases. This magnesium-dependent enzyme catalyzes the hydrolysis of ATP coupled with the transport of the calcium. Defects in this gene cause Hailey-Hailey disease, an autosomal dominant disorder. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq
  • Other Designations:
  • ATP-dependent Ca(2+) pump,ATPase 2C1,ATPase, Ca(2+)-sequestering,HUSSY-28,calcium-transporting ATPase 2C1,secretory pathway Ca2+/Mn2+ ATPase
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