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AMPD1 Polyclonal Antibody

CAT: 0965-JOT-AP00407-01Size: 20 µLDry Ice: NoHazardous: No
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CAT#:0965-JOT-AP00407-01Size:20 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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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.
CAS Number
9007-83-4
Synonyms
AMPD1; AMP deaminase 1; AMP deaminase isoform M; Myoadenylate deaminase
Host
Rabbit
Reactivity
Human;Mouse;Rat
Immunogen
The antiserum was produced against synthesized peptide derived from human AMPD1. AA range:261-310
Clonality
Polyclonal
Applications
IHC-p, ELISA
Stability
-20°C for one year
Concentration
1 mg/ml
Molecular Weight
86490
Antibody Type
Primary antibody
Isotype
IgG