Skip to content

View Spec Sheet

open_in_new
  1. Shop all
  2. Polyclonal

GTX55510

AMPD1 antibody

Cannot supply to this region.

SKU:
GTX55510
Additional Names:
adenosine monophosphate deaminase 1 , MAD , MADA , MMDD
Application:
WB, 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, Mouse, Rat
Buffer:
PBS, 50% Glycerol, 0.02% Sodium azide.
Immunogen:
A synthetic peptide of human AMPD1
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