Anti-Human AGL Polyclonal Antibody

AGL多克隆抗体

This gene encodes the glycogen debrancher enzyme which is involved in glycogen degradation. This enzyme has two independent catalytic activities which occur at different sites on the protein: a 4-alpha-glucotransferase activity and a amylo-1,6-glucosidase activity. Mutations in this gene are associated with glycogen storage disease although a wide range of enzymatic and clinical variability occurs which may be due to tissue-specific alternative splicing. Alternatively spliced transcripts encoding different isoforms have been described. 
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基本信息

数据文档 查看数据文档
货号 PA09282
规格 100μl
宿主 Rabbit
免疫原 Synthetic peptide of human AGL
特异性 Liver, kidney and lymphoblastoid cells express predominantly isoform 1; whereas muscle and heart express not only isoform 1, but also muscle-specific isoform mRNAs (isoforms 2, 3 and 4). Isoforms 5 and 6 are present in both liver and muscle.
亚型 IgG
反应性 Human
克隆
Uniprot P35573
浓度 0.2 mg/mL
推荐稀释度 IHC 1:25-1:100
配方
应用范围 IHC,ELISA
别名 1110061O17Rik,4-1,4-glucantransferase,6-glucosidase,9430004C13Rik,9630046L06Rik,AGL,AI850929,Amylo 1 6 glucosidase 4 alpha glucanotransferase,Amylo-1,Amylo-alpha-1,C77197,Dextrin 6-alpha-D-glucosidase,GDE,GDE,Glycogen debrancher,Glycogen debranching enzyme,Glycogen storage disease type III,Oligo-1
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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