ALDH5A1 抗体 (AA 48-535)
Quick Overview for ALDH5A1 抗体 (AA 48-535) (ABIN5775900)
抗原
See all ALDH5A1 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 48-535
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免疫原
- Recombinant human ALDH5A1 (48-535aa) purified from E. coli
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亚型
- IgG2a kappa
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anti-Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1) (AA 48-535) antibody
ALDH5A1 适用: 人 ELISA, WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1) (C-Term) antibodyALDH5A1 适用: 人, 大鼠, 小鼠 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1) (AA 1-535) antibodyALDH5A1 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1) antibodyALDH5A1 适用: 人, 大鼠, 小鼠 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1) (AA 485-496) antibodyVerified ALDH5A1 适用: 人, 大鼠, 小鼠 ELISA, WB, IHC 宿主: 山羊 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1) (AA 1-535) antibodyALDH5A1 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1) (AA 128-157) antibodyALDH5A1 适用: 人 WB, IHC, FACS, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1) (AA 301-312) antibodyVerified ALDH5A1 适用: 人, 大鼠, 小鼠 ELISA, WB, IHC 宿主: 山羊 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1) (AA 485-496) antibody (Biotin)Verified ALDH5A1 适用: 人 ELISA, WB 宿主: 山羊 Polyclonal Biotin
anti-Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1) (AA 161-210) antibodyALDH5A1 适用: 人, Cow, 兔, 豚鼠, Pig WB 宿主: 兔 Polyclonal unconjugated
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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储存条件
- 4 °C,-20 °C,-80 °C
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储存方法
- Can be stored at +2°C to +8°C for 1 week. For long term storage, aliquot and store at -20°C to -80°C. Avoid repeated freezing and thawing cycles.
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- ALDH5A1 (Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))
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别名
- ALDH5A1
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背景
- This protein belongs to the aldehyde dehydrogenase family of proteins. This gene encodes a mitochondrial NAD+-dependent succinic semialdehyde dehydrogenase. A deficiency of this enzyme, known as 4-hydroxybutyricaciduria, is a rare inborn error in the metabolism of the neurotransmitter gamma-aminobutyric acid (GABA). In response to the defect, physiologic fluids from patients accumulate GHB, a compound with numerous neuromodulatory properties. Two transcript variants encoding distinct isoforms have been identified for this gene.
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NCBI登录号
- NP_001071
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途径
- Monocarboxylic Acid Catabolic Process
抗原
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