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Please note: We are reviewing Western blot images included in the antibody testing data in our catalog, including those provided by third parties. Unless expressly labeled or annotated as “raw-unedited”, Western blot images included in the antibody testing data in our catalog may have been edited, optimized or otherwise adjusted for presentation.
AMPD3 is a member of the AMP deaminase gene family. This protein is a highly regulated enzyme that catalyzes the hydrolytic deamination of adenosine monophosphate to inosine monophosphate, a branch point in the adenylate catabolic pathway. The protein is the erythrocyte (E) isoforms, whereas other family members isoforms predominate in muscle (M) and liver (L) cells. Mutations in this gene lead to the clinically asymptomatic, autosomal recessive condition erythrocyte AMP deaminase deficiency.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: AMP deaminase 3; AMP deaminase H-type; AMP deaminase isoform E; Erythrocyte AMP deaminase; Heart-type AMPD
基因别名: AMPD3
UniProt ID: (Mouse) O08739
Entrez Gene ID: (Mouse) 11717