ALDH3A2 抗体 (AA 101-200)
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- 抗原 See all ALDH3A2 抗体
- ALDH3A2 (Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2))
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抗原表位
- AA 101-200
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适用
- 人
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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 ALDH3A2 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunocytochemistry (ICC)
- 预测反应
- Human,Mouse,Rat
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human ALDH3A2
- 亚型
- IgG
- Top Product
- Discover our top product ALDH3A2 Primary Antibody
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anti-Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) (AA 1-508) antibody
ALDH3A2 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) (AA 1-508) antibodyALDH3A2 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) antibodyALDH3A2 适用: 人, 大鼠, 猴, 犬 WB 宿主: 小鼠 Monoclonal 2D3 unconjugated
anti-Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) (Internal Region) antibodyVerified ALDH3A2 适用: 人, 大鼠 WB, ELISA, IHC 宿主: 山羊 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) (AA 250-320) antibodyALDH3A2 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) (C-Term) antibodyALDH3A2 适用: 人, 大鼠, 小鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) (C-Term) antibodyALDH3A2 适用: 人, 大鼠, 小鼠, 兔, Cow, 犬, 豚鼠, 马, Pig WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) (AA 179-228) antibodyALDH3A2 适用: 人, 大鼠, 小鼠, 兔, 猴, Cow, 犬, 豚鼠, 马, Pig, 小鸡, Bat, 非洲爪蟾, 斑马鱼 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) (AA 1-100) antibodyALDH3A2 适用: 人, 大鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2) antibodyALDH3A2 适用: 人 WB, IHC (p) 宿主: 小鼠 Monoclonal 151CT1-3-1 unconjugated
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- 应用备注
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- ALDH3A2 (Aldehyde Dehydrogenase 3 Family, Member A2 (ALDH3A2))
- 别名
- ALDH3A2 (ALDH3A2 产品)
- 背景
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Synonyms: Ahd 3, Ahd 3r, Ahd3, Ahd3 r, AL3A2_HUMAN, Aldehyde dehydrogenase 10, Aldehyde dehydrogenase 3, Aldehyde dehydrogenase 3 family, member A2, Aldehyde dehydrogenase family 3 member A2, Aldehyde dehydrogenase family 3, subfamily A2, Aldehyde dehydrogenase, family 3, subfamily A, member 2, ALDH10, Aldh3, ALDH3A2, Aldh4, Aldh4 r, Aldh4r, FALDH, Fatty aldehyde dehydrogenase, FLJ20851, Microsomal aldehyde dehydrogenase, msALDH, SLS.
Background: Aldehyde dehydrogenases (ALDHs) mediate the NADP+-dependent oxidation of aldehydes into acids and play an important role in the detoxification of alcohol-derived acetaldehyde, as well as in lipid peroxidation and in the metabolism of corticosteroids, biogenic amines and neurotransmitters. ALDH3A2 (aldehyde dehydrogenase 3 family, member A2), also known as SLS, FALDH or ALDH10, is a 485 amino acid single-pass membrane protein that localizes to the cytoplasmic side of the endoplasmic reticulum and belongs to the aldehyde dehydrogenase family. Expressed in a variety of tissues, including liver, heart, lung, brain, kidney and placenta, ALDH3A2 catalyzes the NAD+-dependent oxidation of long-chain aliphatic aldehydes to fatty acids, a process that is necessary for detoxification and lipid metabolism. Defects in the gene encoding ALDH3A2 are the cause of Sjoegren-Larsson syndrome (SLS), an autosomal recessive neurocutaneous disorder characterized by severe mental retardation, seizures and speech defects. Multiple isoforms of ALDH3A2 exist due to alternative splicing events.
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