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AMPD3 monoclonal antibody, clone AMPD3/901

  • Catalog # : MAB13288
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  • Specification
  • Product Description:
  • Mouse monoclonal antibody raised against full length recombinant human AMPD3.
  • Immunogen:
  • Recombinant protein corresponding to full length human AMPD3.
  • Host:
  • Mouse
  • Theoretical MW (kDa):
  • ~90
  • Reactivity:
  • Human
  • Form:
  • Liquid
  • Purification:
  • Protein A/G purification
  • Isotype:
  • IgG2b, kappa
  • Recommend Usage:
  • Flow Cytometry (1-2 ug/106 cells in 0.1 mL)
    Immunocytochemistry (1-2 ug/mL)
    Immunofluorescence (0.5-1 ug/mL)
    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (2-4 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In 10 mM PBS.
  • Storage Instruction:
  • Store at -20 to -80°C.
    Aliquot to avoid repeated freezing and thawing.
  • Applications
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemical staining (Formalin-fixed paraffin-embedded sections) of human tonsil (A) and human placenta (B) with AMPD3 monoclonal antibody, clone AMPD3/901 (Cat # MAB13288).
  • Immunocytochemistry
  • Immunofluorescence
  • Flow Cytometry
  • Application Image
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
  • enlarge
  • Immunocytochemistry
  • Immunofluorescence
  • Flow Cytometry
  • Gene Information
  • Entrez GeneID:
  • 272
  • Gene Name:
  • AMPD3
  • Gene Alias:
  • -
  • Gene Description:
  • adenosine monophosphate deaminase (isoform E)
  • Gene Summary:
  • This gene encodes a member of the AMP deaminase gene family. The encoded protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. This gene encodes the erythrocyte (E) isoforms, whereas other family members encode isoforms that predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency. Alternatively spliced transcript variants encoding different isoforms of this gene have been described. [provided by RefSeq
  • Other Designations:
  • AMP aminohydrolase,AMP deaminase 3,adenosine monophosphate deaminase 3,erythrocyte type AMP deaminase,erythrocyte-specific AMP deaminase,myoadenylate deaminase
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