AMPD1 Antibody (Center) Blocking Peptide
€363.00
In stock
SKU
AC-BP9591c
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.
Other Names:
AMP deaminase 1, AMP deaminase isoform M, Myoadenylate deaminase, AMPD1
Gene Name: AMPD1 (HGNC:468)
Gene ID: 270
Primary Accession: P23109
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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.
Other Names:
AMP deaminase 1, AMP deaminase isoform M, Myoadenylate deaminase, AMPD1
Gene Name: AMPD1 (HGNC:468)
Gene ID: 270
Primary Accession: P23109
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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