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IHC-P analysis of human heart tissue using GTX46734 ATP2C1 antibody at 1:100. Left to right : DAPI, ATP2C1, Merge. Low pH, heat-induced antigen retrieval method utilizing Sodium Citrate buffer.
IHC-P analysis of human heart tissue using GTX46734 ATP2C1 antibody at 1:100. Left to right : DAPI, ATP2C1, Merge. Low pH, heat-induced antigen retrieval method utilizing Sodium Citrate buffer.
IHC-P analysis of human heart tissue using GTX46734 ATP2C1 antibody at 1:100. Left to right : DAPI, ATP2C1, Merge. Low pH, heat-induced antigen retrieval method utilizing Sodium Citrate buffer.

ATP2C1 antibody, C-term

GTX46734
GeneTex
ApplicationsWestern Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetATP2C1
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Overview

  • Supplier
    GeneTex
  • Product Name
    ATP2C1 antibody, C-term
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 0.2-2.5 ug/ml. IHC-P: 2-10 ug/ml. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot, ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    0.5-1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID27032
  • Target name
    ATP2C1
  • Target description
    ATPase secretory pathway Ca2+ transporting 1
  • Target synonyms
    ATP2C1A; ATPase 2C1; ATPase, Ca(2+)-sequestering; ATPase, Ca++ transporting, type 2C, member 1; ATP-dependent Ca(2+) pump PMR1; BCPM; Ca(2+)/Mn(2+)-ATPase 2C1; calcium-transporting ATPase type 2C member 1; HHD; hSPCA1; HUSSY-28; PMR1; secretory pathway Ca(2+)-transporting ATPase type 1; secretory pathway Ca2+/Mn2+ ATPase 1; SPCA1
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDP98194
  • Protein Name
    Calcium-transporting ATPase type 2C member 1
  • Scientific Description
    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 calcium ions. 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, Aug 2011]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203