GTX86973
AMPD1 antibody
Cannot supply to this region.
- SKU:
- GTX86973
- Additional Names:
- AMPD1 , MAD , MADA , MMDD , adenosine monophosphate deaminase 1
- Application:
- IHC-P
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- PBS, 150mM NaCl, 50% Glycerol, 0.02% Sodium azide.
- Immunogen:
- The antiserum was produced against synthesized peptide derived from human AMPD1 (261-310).
- Uniprot:
- P23109
- Synonyms:
- adenosine monophosphate deaminase 1 (isoform M);adenosine monophosphate deaminase-1 (muscle);AMP deaminase 1;AMP deaminase isoform M;AMPD;MAD;MADA;MMDD;myoadenylate deaminase;skeletal muscle AMPD
- Extra Details:
- 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.[provided by RefSeq, Feb 2010]
- Shipping Conditions:
- Blue Ice