BAAT 抗体
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- 抗原 See all BAAT 抗体
- BAAT (Bile Acid CoA: Amino Acid N-Acyltransferase (Glycine N-Choloyltransferase) (BAAT))
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适用
- 人, 小鼠, 大鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This BAAT antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human BAAT
- 亚型
- IgG
- Top Product
- Discover our top product BAAT Primary Antibody
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- 应用备注
- WB 1:500 - 1:2000
- 限制
- 仅限研究用
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- 浓度
- 1 mg/mL
- 缓冲液
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- 抗原
- BAAT (Bile Acid CoA: Amino Acid N-Acyltransferase (Glycine N-Choloyltransferase) (BAAT))
- 别名
- BAAT (BAAT 产品)
- 别名
- BACAT antibody, BAT antibody, AI118337 antibody, AI158864 antibody, kan-1 antibody, BAAT antibody, bile acid-CoA:amino acid N-acyltransferase antibody, Bile acid-CoA:amino acid N-acyltransferase antibody, bile acid-Coenzyme A: amino acid N-acyltransferase antibody, bile acid CoA:amino acid N-acyltransferase antibody, BAAT antibody, RPIC_RS10270 antibody, Bcav_2277 antibody, Rpic12D_1765 antibody, Baat antibody, LOC481635 antibody, LOC100054567 antibody, LOC786798 antibody
- 背景
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Synonyms: FLJ20300,BAAT,BAAT,BACAT,BAT,Bile acid CoA: amino acid N-acyltransferase (glycine N-choloyltransferase),Bile acid CoA:amino acid N acyltransferase,Bile acid Coenzyme A amino acid N acyltransferase glycine N choloyltransferase,Bile acid Coenzyme A: amino acid N acyltransferase,Bile acid-CoA:amino acid N-acyltransferase,Glycine N choloyltransferase,Glycine N-choloyltransferase,Long chain fatty acyl CoA hydrolase,Long-chain fatty-acyl-CoA hydrolase,MGC104432
Background: The protein encoded by this gene is a liver enzyme that catalyzes the transfer of C24 bile acids from the acyl-CoA thioester to either glycine or taurine, the second step in the formation of bile acid-amino acid conjugates. The bile acid conjugates then act as a detergent in the gastrointestinal tract, which enhances lipid and fat-soluble vitamin absorption. Defects in this gene are a cause of familial hypercholanemia (FHCA). Two transcript variants encoding the same protein have been found for this gene.
- 分子量
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Observed_MW: 46kDa
Calculated_MW: 46kDa
- 基因ID
- 570
- UniProt
- Q14032
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