AMPD1 Polyclonal Antibody

• Background:

  Adenosine monophosphate deaminase 1 catalyzes the deamination of AMP to IMP in skeletal muscle and plays an important role in the purine nucleotide cycle. Two other genes have been identified, AMPD2 and AMPD3, for the liver- and erythocyte-specific isoforms, respectively. Deficiency of the muscle-specific enzyme is apparently a common cause of exercise-induced myopathy and probably the most common cause of metabolic myopathy in the human. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.

• Description:

  This is a AMPD1 Polyclonal Antibody from Reddot Biotech. This product is for Research Use Only.

• Synonyms:

  Adenosine monophosphate deaminase 1 (isoform M), Adenosine monophosphate deaminase 1, AMP deaminase 1, AMP deaminase isoform M, AMPD 1, AMPD, Ampd01, MAD, MADA, Myoadenylate deaminase, RATAMPD01, Skeletal muscle AMPD

• Swiss Prot:

  P23109

• Accession Number:

  NP_000027

• Reactivity:

  Human

• Immunogen:

  Synthetic peptide of human AMPD1

• Clonality:

  Polyclonal

• Conjugation:

  Unconjugated

• Type:

  Polyclonal Antibody

• Applications:

  WB, IHC, ELISA

• Purification Method:

  Affinity purification

• Assay Type:

  Antibody

• Concentration:

  1 mg/mL

• Dilution:

  WB 1:1000-1:5000, IHC 1:100-1:300

• Buffer:

  PBS with 0.05% sodium azide and 50% glycerol, PH7.4

• Storage Conditions:

  Store at -20°C. Avoid freeze / thaw cycles.

• Calculated Molecular Weight:

  90 kDa

• Host or Source:

  Rabbit

• Isotype:

  IgG