ABHD5 抗体 (N-Term)
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- 抗原 See all ABHD5 抗体
- ABHD5 (Abhydrolase Domain Containing 5 (ABHD5))
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抗原表位
- N-Term
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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 ABHD5 antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 特异性
- ABHD5 antibody was raised against the N terminal of ABHD5
- 纯化方法
- Purified
- 免疫原
- ABHD5 antibody was raised using the N terminal of ABHD5 corresponding to a region with amino acids NRPVYAFDLLGFGRSSRPRFDSDAEEVENQFVESIEEWRCALGLDKMILL
- Top Product
- Discover our top product ABHD5 Primary Antibody
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- 应用备注
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WB: 5 µg/mL
Optimal conditions should be determined by the investigator. - 说明
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ABHD5 Blocking Peptide, catalog no. 33R-6861, is also available for use as a blocking control in assays to test for specificity of this ABHD5 antibody
- 限制
- 仅限研究用
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- 状态
- Lyophilized
- 溶解方式
- Lyophilized powder. Add distilled water for a 1 mg/mL concentration of ABHD5 antibody in PBS
- 浓度
- Lot specific
- 缓冲液
- PBS
- 注意事项
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Avoid repeated freeze/thaw cycles.
Dilute only prior to immediate use. - 储存条件
- 4 °C/-20 °C
- 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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- 抗原
- ABHD5 (Abhydrolase Domain Containing 5 (ABHD5))
- 别名
- ABHD5 (ABHD5 产品)
- 别名
- ABHD5 antibody, cds antibody, cgi58 antibody, iecn2 antibody, ncie2 antibody, abhd5 antibody, CDS antibody, CGI58 antibody, IECN2 antibody, NCIE2 antibody, 1300003D03Rik antibody, 2010002J10Rik antibody, CGI-58 antibody, IECN5 antibody, abhydrolase domain containing 5 antibody, abhydrolase domain containing 5a antibody, abhydrolase domain containing 5 L homeolog antibody, ABHD5 antibody, abhd5 antibody, abhd5a antibody, Abhd5 antibody, abhd5.L antibody
- 背景
- ABHD5 belongs to a large family of proteins defined by an alpha/beta hydrolase fold, and contains three sequence motifs that correspond to a catalytic triad found in the esterase/lipase/thioesterase subfamily. It differs from other members of this subfamily in that its putative catalytic triad contains an asparagine instead of the serine residue. Mutations in ABHD5 gene have been associated with Chanarin-Dorfman syndrome, a triglyceride storage disease with impaired long-chain fatty acid oxidation.
- 分子量
- 39 kDa (MW of target protein)
- 途径
- Lipid Metabolism
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