DLD 抗体
Quick Overview for DLD 抗体 (ABIN2719487)
抗原
See all DLD 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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产品特性
- Homo sapiens dihydrolipoamide dehydrogenase (DLD)
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纯化方法
- Purified from mouse ascites fluids by affinity chromatography
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免疫原
- Full length human recombinant protein of human DLD(NP_000099) produced in HEK293T cell.
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亚型
- IgG1
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anti-Dihydrolipoamide Dehydrogenase (DLD) (AA 45-271) antibody
DLD 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Dihydrolipoamide Dehydrogenase (DLD) antibodyDLD 适用: 大鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Dihydrolipoamide Dehydrogenase (DLD) antibodyDLD 适用: 人 WB, IHC, IF 宿主: 兔 Monoclonal unconjugated
anti-Dihydrolipoamide Dehydrogenase (DLD) antibodyKO Validated DLD 适用: 人 WB, IF, ICC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Dihydrolipoamide Dehydrogenase (DLD) (AA 36-300) antibodyDLD 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Dihydrolipoamide Dehydrogenase (DLD) (AA 1-509) antibodyDLD 适用: 人 WB, ELISA, IHC (p) 宿主: 小鼠 Monoclonal 3C1 unconjugated
anti-Dihydrolipoamide Dehydrogenase (DLD) (AA 238-466) antibodyDLD 适用: 大鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Dihydrolipoamide Dehydrogenase (DLD) antibodyDLD 适用: 人, 小鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Dihydrolipoamide Dehydrogenase (DLD) antibodyDLD 适用: 人, 小鼠, 大鼠, 犬, 猴 WB, IF, FACS 宿主: 小鼠 Monoclonal 5G7 unconjugated
anti-Dihydrolipoamide Dehydrogenase (DLD) (AA 280-487) antibodyDLD 适用: 人 WB, IHC, IF, ICC 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB 1:2000, IF 1:100, FLOW 1:100,
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说明
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The concentration of the product may vary between diferrent lots.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.5-1.0 mg/mL
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缓冲液
- PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 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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- DLD (Dihydrolipoamide Dehydrogenase (DLD))
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别名
- DLD
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背景
- This gene encodes the L protein of the mitochondrial glycine cleavage system. The L protein, also named dihydrolipoamide dehydrogenase, is also a component of the pyruvate dehydrogenase complex, the alpha-ketoglutarate dehydrogenase complex, and the branched-chain alpha-keto acide dehydrogenase complex. Mutations in this gene have been identified in patients with E3-deficient maple syrup urine disease and lipoamide dehydrogenase deficiency.
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分子量
- 50.1 kDa
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基因ID
- 1738
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NCBI登录号
- NM_000108
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HGNC
- 1738
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途径
- Ribonucleoside Biosynthetic Process, Cell RedoxHomeostasis
抗原
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