兔抗AMPD1多克隆抗体

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.

Applications:

ELISA, WB, IHC

Name of antibody:

AMPD1

Immunogen:

Synthetic peptide of human AMPD1

Full name:

adenosine monophosphate deaminase 1

Synonyms：

MAD; MADA

SwissProt:

P23109

ELISA Recommended dilution:

2000-10000

IHC positive control:

Human liver cancer and Human thyroid cancer

IHC Recommend dilution:

100-300

WB Predicted band size:

90 kDa

WB Positive control:

Human fetal muscle tissue

WB Recommended dilution:

500-2000