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ALDH4A1 抗体
ALDH4A1
适用: 人, 小鼠, 大鼠
WB, IHC, ELISA
宿主: 兔
Polyclonal
unconjugated
ALDH4A1抗体详情
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抗原
See all ALDH4A1 抗体
ALDH4A1
(Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1))
适用
All reactivities for ALDH4A1 抗体
人, 小鼠, 大鼠
宿主
All hosts for ALDH4A1 抗体
兔
克隆类型
All clonalities for ALDH4A1 抗体
多克隆
标记
All conjugates for ALDH4A1 抗体
This ALDH4A1 antibody is un-conjugated
应用范围
All applications for ALDH4A1 抗体
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
产品特性
Polyclonal Antibody
纯化方法
Affinity purification
免疫原
Recombinant protein of human ALDH4A1
亚型
IgG
Top Product
Discover our top product ALDH4A1 Primary Antibody
Alternatives
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anti-Aldehyde Dehydrogenase 4 Family, Member A1 (ALDH4A1) (C-Term) antibody
ALDH4A1
适用: 人, 小鼠, 大鼠, Cow, 马, 兔, 斑马鱼, 猴, 非洲爪蟾
WB, IHC, IHC (p)
宿主: 兔
Polyclonal
unconjugated
使用细节
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应用备注
WB 1:500-1:2000, IHC 1:50-1:200
限制
仅限研究用
贮存及处理
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状态
Liquid
浓度
0.3 mg/mL
缓冲液
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
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.
储存条件
-20 °C
储存方法
Store at -20°C. Avoid freeze / thaw cycles.
ALDH4A1目标详情
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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
This protein 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. Alternatively spliced transcript variants encoding different isoforms have been identified for this gene.
分子量
62 kDa
UniProt
P30038
途径
Monocarboxylic Acid Catabolic Process
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