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Last updated: 2018/1/14
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CACNA1H monoclonal antibody, clone S55-10

  • Catalog # : MAB6650
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  • Specification
  • Product Description:
  • Mouse monoclonal antibody raised against partial recombinant CACNA1H.
  • Immunogen:
  • Recombinant fusion protein corresponding to amino acids 1019-1293 (II-III loop) of human CACNA1H.
  • Host:
  • Mouse
  • Reactivity:
  • Human, Mouse, Rat
  • Specificity:
  • Detects ~260KDa. No cross-reactivity against Cav1.3.
  • Form:
  • Liquid
  • Isotype:
  • IgG1
  • Recommend Usage:
  • Western Blot (1-10 ug/mL)
    Immunohistochemistry (0.1-1.0 ug/mL)
    Immunocytochemistry (0.1-1.0 ug/mL)
    Immunofluorescence (1.0-10 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In PBS, pH 7.4 (50% glycerol, 0.09% sodium azide)
  • Storage Instruction:
  • 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.
  • Publication Reference
  • Applications
  • Western Blot
  • Immunocytochemistry
  • Immunofluorescence
  • Immunofluorescence
  • Immunofluorescence staining in human hippocampus with CACNA1H monoclonal antibody, clone S55-10 (Cat # MAB6650).
  • Immunoprecipitation
  • Application Image
  • Western Blot
  • Immunocytochemistry
  • Immunoprecipitation
  • Gene Information
  • Entrez GeneID:
  • 8912
  • Gene Name:
  • Gene Alias:
  • CACNA1HB,Cav3.2,EIG6,FLJ90484
  • Gene Description:
  • calcium channel, voltage-dependent, T type, alpha 1H subunit
  • Gene Summary:
  • This gene encodes a T-type member of the alpha-1 subunit family, a protein in the voltage-dependent calcium channel complex. Calcium channels mediate the influx of calcium ions into the cell upon membrane polarization and consist of a complex of alpha-1, alpha-2/delta, beta, and gamma subunits in a 1:1:1:1 ratio. The alpha-1 subunit has 24 transmembrane segments and forms the pore through which ions pass into the cell. There are multiple isoforms of each of the proteins in the complex, either encoded by different genes or the result of alternative splicing of transcripts. Alternate transcriptional splice variants, encoding different isoforms, have been characterized for the gene described here. Studies suggest certain mutations in this gene lead to childhood absence epilepsy (CAE). [provided by RefSeq
  • Other Designations:
  • calcium channel, voltage-dependent, T type, alpha 1Hb subunit,calcium channel, voltage-dependent, alpha 1H subunit,low-voltage-activated calcium channel alpha1 3.2 subunit,low-voltage-activated calcium channel alpha13.2 subunit,voltage dependent t-type ca
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