BAAT 抗体 (N-Term)
Quick Overview for BAAT 抗体 (N-Term) (ABIN631444)
抗原
See all BAAT 抗体适用
宿主
克隆类型
标记
应用范围
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                                            抗原表位
- N-Term
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                                            特异性
- BAAT antibody was raised against the N terminal of BAAT
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                                            纯化方法
- Affinity purified
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                                            免疫原
- BAAT antibody was raised using the N terminal of BAAT corresponding to a region with amino acids IQLTATPVSALVDEPVHIRATGLIPFQMVSFQASLEDENGDMFYSQAHYR
 
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                                            应用备注
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                        WB: 1 µg/mL
 Optimal conditions should be determined by the investigator.
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                                            说明
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                        BAAT Blocking Peptide, (ABIN939504), is also available for use as a blocking control in assays to test for specificity of this BAAT antibody 
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                                            限制
- 仅限研究用
 
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                                            状态
- Lyophilized
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                                            溶解方式
- Lyophilized powder. Add distilled water for a 1 mg/mL concentration of BAAT antibody in PBS
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                                            浓度
- Lot specific
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                                            缓冲液
- PBS
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                                            注意事项
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                        Avoid repeated freeze/thaw cycles. 
 Dilute only prior to immediate use.
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                                            储存条件
- 4 °C/-20 °C
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                                            储存方法
- Store at 2-8 °C for short periods. For longer periods of storage, store at -20 °C.
 
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    - BAAT (Bile Acid CoA: Amino Acid N-Acyltransferase (Glycine N-Choloyltransferase) (BAAT))
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                                            别名
- BAAT
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                                            背景
- BAAT 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).
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                                            分子量
- 46 kDa (MW of target protein)
 抗原
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