AMPD1 Antibody
Product Specifications
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.
NCBI Gene ID
270
Swiss Prot
P23109
Host
Rabbit
Reactivity
Human, Mouse, Rat
Immunogen
A synthetic peptide of human AMPD1
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cancer, Signal Transduction
Purification
Affinity purification
Positive Control
HT-29
Concentration
Batch dependent
Buffer
PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
Store at -20˚ C. Avoid freeze / thaw cycles.
Calculated Molecular Weight
Observed: 80kDa
Fragment
IgG
Symbol
AMPD1
Positive Control 2
Mouse skeletal muscle
Positive Control 3
Mouse thymus
Positive Control 4
Mouse pancreas
NCBI Official Name
Adenosine monophosphate deaminase 1
NCBI Organism
Homo sapiens
Other Product Names
AMPD1, adenosine monophosphate deaminase 1 (isoform M), MAD, MADA, Adenosine monophosphate deaminase-1 (muscle), OTTHUMP00000059283, MMDD
Tested Applications
WB, IHC
Physical Properties
Liquid
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