AMPD1 antibody

Catalog No. ABIN6571423

Product Details anti-AMPD1 Antibody

Target: AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This AMPD1 antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Purification: Affinity purification

Immunogen: A synthetic peptide of human AMPD1

Isotype: IgG

Application Details

Application Notes: WB 1:500 - 1:2000 IHC 1:50 - 1:100

Restrictions: For Research Use only

Handling

Concentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

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

Target Details for AMPD1

Target: AMPD1 (Adenosine Monophosphate Deaminase 1 (AMPD1))

Alternative Name: AMPD1 (AMPD1 Products)

Synonyms: ampd1 antibody, MAD antibody, MADA antibody, AI553520 antibody, Ampd-1 antibody, Ampd01 antibody, RATAMPD01 antibody, zgc:77905 antibody, adenosine monophosphate deaminase 1 antibody, N-acetyl-anhydromuranmyl-L-alanine amidase antibody, N-acetylmuramoyl-L-alanine amidase antibody, Negative regulator of beta-lactamase expression antibody, adenosine monophosphate deaminase 1 (isoform M) antibody, AMPD1 antibody, ampD1 antibody, ampd1 antibody, Ampd1 antibody

Background:

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

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.

Molecular Weight:

Observed_MW: 80kDa

Calculated_MW: 89kDa/90kDa

Gene ID: 270

UniProt: P23109