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AMPD1 Polyclonal Antibody, Invitrogen™
Rabbit Polyclonal Antibody
Brand: Thermo Scientific PA555316
Additional Details : Weight : 0.02000kg
Description
Immunogen sequence: SETSSTKLSH IDEYISSSPT YQTVPDFQRV QITGDYASGV TVEDFEIVCK GLYRALCIRE KYMQKSFQRF PKTPSKYLRN IDGEAWVANE Highest antigen sequence identity to the following orthologs: Mouse - 92%, Rat - 92%.
AMP deaminase (AMPD) is an allosteric enzyme involved in the regulation of adenosine metabolism. It catalyzes a central reaction in purine nucleotide biosynthesis where AMP is deaminated to IMP, liberating ammonia. There are three functional isoforms of AMPD. AMPD1 (E.C. No 3.5.4.6.) is the skeletal muscle-specific isoform M located in type II muscle fibers, neuromuscular junctions and in capillaries. This protein is the predominant member of AMPD multi-gene family and is considered as the sensor of the cell’s changing energy requirements. AMPD1 deficiency causes irregular muscle metabolism due to lower rate of ATP degradation, phosphocreatine hydrolysis and accumulation of lactic acid. Mutated AMPD1 expression has been detected in neuromuscular disorders, exercise-induced skeletal muscle myopathies and congestive heart failures due to coronary artery diseases.Specifications
AMPD1 | |
Polyclonal | |
Unconjugated | |
AMPD1 | |
adenosine monophosphate deaminase 1; adenosine monophosphate deaminase 1 (isoform M); adenosine monophosphate deaminase-1 (muscle); AI553520; AMP deaminase 1; AMP deaminase isoform M; Ampd; Ampd01; AMPD1; Ampd-1; MAD; MADA; MMDD; myoadenylate deaminase; RATAMPD01; RP5-1000E10.1; skeletal muscle AMPD | |
Rabbit | |
Antigen affinity chromatography | |
RUO | |
270 | |
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
Liquid |
Immunohistochemistry | |
0.2 mg/mL | |
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2 | |
P23109 | |
AMPD1 | |
Recombinant protein corresponding to Human AMPD1 | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
Research Use Only