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AMPD1 Antibody

https://www.academycancerimmunology.org/web/image/product.template/4223/image_1920?unique=d05de28
Size : 50 µL Clone Number: Aliases: AMPD1AMP deaminase 1 antibody; EC 3.5.4.6 antibody; AMP deaminase isoform M antibody; Myoadenylate deaminase antibody Product Type: Polyclonal Antibody Immunogen Species: Homo sapiens (Human) UniProt ID: P23109 Immunogen: Synthetic peptide of Human AMPD1 Host: Rabbit Reactivity: Human Tested Applications: ELISA, WB, IHC; ELISA: 1: 2000-1: 10000, WB: 1: 500-1: 2000, IHC: 1: 100-1: 300 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. Clonality: Polyclonal Isotype: IgG Purification Method: Antigen affinity purification Conjugate: Non-conjugated Buffer: -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol Form: Liquid Stroage: Upon receipt, store at -20°C or -80°C. Avoid repeated freeze. Target Names: AMPD1 Research Areas: Cancer;Metabolism;Signal transduction

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