Anti-Human AMPD1 Polyclonal Antibody

AMPD1多克隆抗体

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.
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基本信息

数据文档 查看数据文档
货号 PA09973
规格 100μl
宿主 Rabbit
免疫原 Synthetic peptide of human AMPD1
特异性
亚型 IgG
反应性 Human
克隆
Uniprot P23109
浓度 0.5 mg/mL
推荐稀释度 WB 1:500-1:2000, IHC 1:100-1:300
配方
应用范围 WB,IHC,ELISA
别名 Adenosine monophosphate deaminase 1 (isoform M),Adenosine monophosphate deaminase 1,AMP deaminase 1,AMP deaminase isoform M,AMPD 1,AMPD,Ampd01,MAD,MADA,Myoadenylate deaminase,RATAMPD01,Skeletal muscle AMPD
保存条件 冻干产品: 2 - 8°C保存5年; 液体: -20°C保存2年.
注意 仅用于科学研究, 不能用于疾病诊断.

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