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ALDH5A1 抗体 (Internal Region)
ALDH5A1
适用: 人, 大鼠, 小鼠, Cow, 犬
WB, EIA
宿主: 山羊
Polyclonal
unconjugated
ALDH5A1抗体详情
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抗原
See all ALDH5A1 抗体
ALDH5A1
(Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))
抗原表位
All epitopes for ALDH5A1 抗体
AA 301-312, Internal Region
适用
All reactivities for ALDH5A1 抗体
人, 大鼠, 小鼠, Cow, 犬
宿主
All hosts for ALDH5A1 抗体
山羊
克隆类型
All clonalities for ALDH5A1 抗体
多克隆
标记
All conjugates for ALDH5A1 抗体
This ALDH5A1 antibody is un-conjugated
应用范围
All applications for ALDH5A1 抗体
Western Blotting (WB), Enzyme Immunoassay (EIA)
序列
C-TGKILLHHAA NS
特异性
This antibody is expected to recognize both reported isoforms (NP_733936.1, NP_001071.1).
交叉反应 (详细)
Species reactivity (expected):Canine (Dog), Bovine. Species reactivity (tested):Human, Mouse, Rat.
纯化方法
Ammonium Sulphate Precipitation followed by antigen Affinity Chromatography using the immunizing peptide
免疫原
Peptide with sequence from the internal region of the protein sequence according to NP_733936.1 NP_001071.1.
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使用细节
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应用备注
Optimal working dilution should be determined by the investigator.
限制
仅限研究用
贮存及处理
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浓度
0.5 mg/mL
缓冲液
Tris saline, pH ~7.3 with 0.02 % Sodium Azide and 0.5 % BSA
储存液
Sodium azide
注意事项
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
注意事项
Avoid repeated freezing and thawing.
储存条件
4 °C/-20 °C
储存方法
Store the antibody undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
ALDH5A1目标详情
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抗原
ALDH5A1
(Aldehyde Dehydrogenase 5 Family, Member A1 (ALDH5A1))
别名
ALDH5A1 / SSADH (ALDH5A1 产品 )
别名
SSADH antibody, SSDH antibody, Ssadh antibody, 6330403E24Rik antibody, Ahd-1 antibody, Ahd1 antibody, D630032B01Rik antibody, OTTMUSG00000000613 antibody, Ssdh1 antibody, aldehyde dehydrogenase 5 family member A1 antibody, aldehyde dehydrogenase 5 family, member A1 antibody, aldhehyde dehydrogenase family 5, subfamily A1 antibody, ALDH5A1 antibody, aldh5a1 antibody, Aldh5a1 antibody
背景
Defects in ALDH5A1 are the cause of succinate semialdehyde dehydrogenase deficiency (SSADH deficiency) [MIM:271980]. SSADH deficiency is a rare inborn error in the metabolism of 4-aminobutyric acid (GABA) which leads to accumulation of 4-hydroxybutyric acid in physiologic fluids of patients. The disease is characterized by severe ataxia and by mildly retarded psychomotor development.Synonyms: Aldehyde dehydrogenase family 5 member A1, NAD(+)-dependent succinic semialdehyde dehydrogenase, Succinate-semialdehyde dehydrogenase, mitochondrial
分子量
58.7kDa (NP_733936.1).
基因ID
7915
NCBI登录号
NP_001071
UniProt
P51649
途径
Monocarboxylic Acid Catabolic Process
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