alpha KGDHC 抗体 (AA 1-1023) (Fluoro594)
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北京 101111
Quick Overview for alpha KGDHC 抗体 (AA 1-1023) (Fluoro594) (ABIN7967842)
抗原
See all alpha KGDHC (alphaKGDHC) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 1-1023
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原理
- Anti-OGDH Antibody Fluoro594 Conjugated
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交叉反应 （详细）
- No cross-reactivity with other proteins.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E.coli-derived human OGDH recombinant protein (Position: M1-S1023).
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亚型
- IgG
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anti-alpha Ketoglutarate Dehydrogenase (alphaKGDHC) (C-Term) antibody
alphaKGDHC 适用: 人 WB, IF, ICC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-alpha Ketoglutarate Dehydrogenase (alphaKGDHC) (AA 381-410), (C-Term) antibodyalphaKGDHC 适用: 人 WB, IHC (p) 宿主: 兔 Polyclonal RB32469 unconjugated
anti-alpha Ketoglutarate Dehydrogenase (alphaKGDHC) (N-Term) antibodyalphaKGDHC 适用: 人, Cow, 马, Bat, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-alpha Ketoglutarate Dehydrogenase (alphaKGDHC) (AA 41-423) antibodyalphaKGDHC 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-alpha Ketoglutarate Dehydrogenase (alphaKGDHC) (N-Term) antibodyalphaKGDHC 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-alpha Ketoglutarate Dehydrogenase (alphaKGDHC) (AA 1-1023) antibodyalphaKGDHC 适用: 人, 小鼠, 大鼠 WB, ELISA, FACS 宿主: 兔 Polyclonal unconjugated
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应用备注
- Flow Cytometry, Optimal dilutions should be determined by end users.
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
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有效期
- 12 months
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- alpha KGDHC (alphaKGDHC) (alpha Ketoglutarate Dehydrogenase (alphaKGDHC))
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别名
- OGDH
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背景
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Background: Alpha-ketoglutarate dehydrogenase also known as 2-oxoglutarate dehydrogenase E1 component, mitochondrial is an enzyme that in humans is encoded by the OGDH gene. This gene encodes one subunit of the 2-oxoglutarate dehydrogenase complex. This complex catalyzes the overall conversion of 2-oxoglutarate (alpha-ketoglutarate) to succinyl-CoA and CO(2) during the Krebs cycle. The protein is located in the mitochondrial matrix and uses thiamine pyrophosphate as a cofactor. A congenital deficiency in 2-oxoglutarate dehydrogenase activity is believed to lead to hypotonia, metabolic acidosis, and hyperlactatemia. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[
Gene Full Name: oxoglutarate dehydrogenase
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基因ID
- 4967
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UniProt
- Q02218
抗原
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