ALDH4A1 抗体 (C-Term)
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- 抗原 See all ALDH4A1 抗体
- ALDH4A1 (Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))
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抗原表位
- C-Term
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适用
- 人, 小鼠, 犬, 斑马鱼
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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 ALDH4A1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC)
- 特异性
- ALDH4 A1 antibody was raised against the C terminal of ALDH4 1
- 纯化方法
- Purified
- 免疫原
- ALDH4 A1 antibody was raised using the C terminal of ALDH4 1 corresponding to a region with amino acids RNAAGNFYINDKSTGSIVGQQPFGGARASGTNDKPGGPHYILRWTSPQVI
- Top Product
- Discover our top product ALDH4A1 Primary Antibody
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- 应用备注
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WB: 1.25 µg/mL, IHC: 4-8 µg/mL
Optimal conditions should be determined by the investigator. - 说明
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ALDH4A1 Blocking Peptide, catalog no. 33R-8071, is also available for use as a blocking control in assays to test for specificity of this ALDH4A1 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 ALDH0 1 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
- ALDH4A1 (Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))
- 别名
- ALDH4A1 (ALDH4A1 产品)
- 别名
- aldh4 antibody, p5cd antibody, p5cdh antibody, ALDH4 antibody, P5CD antibody, P5CDh antibody, A930035F14Rik antibody, Ahd-1 antibody, Ahd1 antibody, Aldh4 antibody, Aldh5a1 antibody, E330022C09 antibody, P5cd antibody, P5cdh antibody, P5cdhl antibody, P5cdhs antibody, Ssdh1 antibody, zgc:63592 antibody, aldehyde dehydrogenase 4 family member A1 antibody, aldehyde dehydrogenase 4 family, member A1 antibody, aldehyde dehydrogenase 4 family member A1 L homeolog antibody, aldh4a1 antibody, ALDH4A1 antibody, Aldh4a1 antibody, aldh4a1.L antibody
- 背景
- ALDH4A1 belongs to the aldehyde dehydrogenase family of proteins. This enzyme is a mitochondrial matrix NAD-dependent dehydrogenase which catalyzes the second step of the proline degradation pathway, converting pyrroline-5-carboxylate to glutamate. Deficiency of this enzyme is associated with type II hyperprolinemia, an autosomal recessive disorder characterized by accumulation of delta-1-pyrroline-5-carboxylate (P5C) and proline.
- 分子量
- 62 kDa (MW of target protein)
- 途径
- Monocarboxylic Acid Catabolic Process
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