MECR 抗体 (AA 39-359)
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Quick Overview for MECR 抗体 (AA 39-359) (ABIN7874598)
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
- MECR Antibody / 2-Enoyl thioester reductase
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纯化方法
- Antigen affinity purified
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免疫原
- An E.coli-derived human recombinant protein (E39-A359) was used as the immunogen for the MECR antibody.
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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) (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
anti-Mitochondrial Trans-2-Enoyl-CoA Reductase (MECR) (AA 201-229) antibodyMECR 适用: 人 WB 宿主: 兔 Polyclonal RB42835 unconjugated
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应用备注
- Optimal dilution of the MECR antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the MECR antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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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
- 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.
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UniProt
- Q9BV79
抗原
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