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IHC-P analysis of human tonsil tissue using GTX34411 AMPD3 antibody [AMPD3/901].
IHC-P analysis of human tonsil tissue using GTX34411 AMPD3 antibody [AMPD3/901].
IHC-P analysis of human tonsil tissue using GTX34411 AMPD3 antibody [AMPD3/901].

AMPD3 antibody [AMPD3/901]

GTX34411
GeneTex
ApplicationsImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
Product group Antibodies
ReactivityHuman
TargetAMPD3
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Overview

  • Supplier
    GeneTex
  • Product Name
    AMPD3 antibody [AMPD3/901]
  • Delivery Days Customer
    9
  • Antibody Specificity
    This antibody recognizes a protein of ~90kDa, which is identified as Adenosine Monophosphate Deaminase, isoform E (AMPD3). It shows reactivity with cells of the erythroid lineage at all stages of maturation in the peripheral blood, bone marrow, and fetal
  • Application Supplier Note
    IHC-P: 2-4microg/ml for 30 minutes at RT. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoHistoChemistry, ImmunoHistoChemistry Paraffin
  • Certification
    Research Use Only
  • Clonality
    Monoclonal
  • Clone ID
    AMPD3/901
  • Concentration
    0.2 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID272
  • Target name
    AMPD3
  • Target description
    adenosine monophosphate deaminase 3
  • Target synonyms
    adenosine monophosphate deaminase (isoform E); AMP aminohydrolase; AMP deaminase 3; erythrocyte AMP deaminase; erythrocyte type AMP deaminase; erythrocyte-specific AMP deaminase; myoadenylate deaminase
  • Host
    Mouse
  • Isotype
    IgG2b
  • Protein IDQ01432
  • Protein Name
    AMP deaminase 3
  • Scientific Description
    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, Jul 2008]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203