MECR 抗体 (AA 39-359) (FITC)
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北京 101111
Quick Overview for MECR 抗体 (AA 39-359) (FITC) (ABIN8010767)
抗原
See all MECR 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 39-359
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原理
- Anti-MECR Antibody FITC 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 MECR recombinant protein (Position: E39-A359).
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亚型
- IgG
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anti-Mitochondrial Trans-2-Enoyl-CoA Reductase (MECR) antibody
MECR 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Mitochondrial Trans-2-Enoyl-CoA Reductase (MECR) (AA 1-373) antibodyMECR 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-Mitochondrial Trans-2-Enoyl-CoA Reductase (MECR) (AA 211-373) antibodyMECR 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Mitochondrial Trans-2-Enoyl-CoA Reductase (MECR) (AA 1-373) antibodyMECR 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Mitochondrial Trans-2-Enoyl-CoA Reductase (MECR) (AA 201-229) antibodyMECR 适用: 人 WB 宿主: 兔 Polyclonal RB42835 unconjugated
anti-Mitochondrial Trans-2-Enoyl-CoA Reductase (MECR) (C-Term) antibodyMECR 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Mitochondrial Trans-2-Enoyl-CoA Reductase (MECR) (AA 167-216) antibodyMECR 适用: 人, 小鼠, 大鼠, Cow, Pig, 犬, 马, 兔, Bat, 猴, Hamster WB 宿主: 兔 Polyclonal unconjugated
anti-Mitochondrial Trans-2-Enoyl-CoA Reductase (MECR) (AA 289-338) antibodyMECR 适用: 人, 小鼠, 大鼠, Cow, Pig, Bat, 猴 WB 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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- MECR (Mitochondrial Trans-2-Enoyl-CoA Reductase (MECR))
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别名
- MECR
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背景
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Background: Trans-2-enoyl-CoA reductase, mitochondrial is an enzyme that in humans is encoded by the MECR gene. The protein encoded by this gene is an oxidoreductase that catalyzes the last step in mitochondrial fatty acid synthesis. Defects in this gene are a cause of childhood-onset dystonia and optic atrophy.
Gene Full Name: mitochondrial trans-2-enoyl-CoA reductase
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基因ID
- 51102
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UniProt
- Q9BV79
抗原
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