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Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD) (AA 1-220) 抗体

Cited in 1 publication. This anti-Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial antibody is a 兔 多克隆 antibody detecting Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial in WB 和 IF. Suitable for 人.
产品编号 ABIN1678521
发货至: 中国
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Quick Overview for Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD) (AA 1-220) 抗体 (ABIN1678521)

抗原

Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD)

适用

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宿主

  • 83
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克隆类型

  • 55
  • 34
多克隆

标记

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非结合性

应用范围

  • 61
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Western Blotting (WB), Immunofluorescence (IF)
  • 抗原表位

    • 15
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    AA 1-220

    序列

    MAAGFGRCCR VLRSISRFHW RSQHTKANRQ REPGLGFSFE FTEQQKEFQA TARKFAREEI IPVAAEYDKT GEYPVPLIRR AWELGLMNTH IPENCGGLGL GTFDACLISE ELAYGCTGVQ TAIEGNSLGQ MPIIIAGNDQ QKKKYLGRMT EEPLMCAYCV TEPGAGSDVA GIKTKAEKKG DEYIINGQKM WITNGGKANW YFLLARSDPD PKAPANKAFT

    交叉反应

    人, 小鼠, 大鼠

    产品特性

    Polyclonal Antibodies

    纯化方法

    Affinity purification

    免疫原

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-220 of human ACADM (NP_000007.1).

    亚型

    IgG
  • 应用备注

    WB,1:500 - 1:2000,IF,1:50 - 1:200

    限制

    仅限研究用
  • 缓冲液

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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.
  • Fan, Long, Yan, Wang, Shi, Bao, Hu, Li, Chen, Zheng, Yan: "Dietary leucine supplementation alters energy metabolism and induces slow-to-fast transitions in longissimus dorsi muscle of weanling piglets." in: The British journal of nutrition, Vol. 117, Issue 9, pp. 1222-1234, (2017) (PubMed).

  • 抗原

    Medium-Chain Specific Acyl-CoA Dehydrogenase, Mitochondrial (MCAD)

    别名

    ACADM

    背景

    This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Defects in this gene cause medium-chain acyl-CoA dehydrogenase deficiency, a disease characterized by hepatic dysfunction, fasting hypoglycemia, and encephalopathy, which can result in infantile death. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.,ACADM,ACAD1,MCAD,MCADH,Cancer,Signal Transduction,Endocrine & Metabolism,Mitochondrial metabolism,Mitochondrial markers,Lipid Metabolism,Cardiovascular,Lipids,Fatty Acids,ACADM

    分子量

    46 kDa/47 kDa

    基因ID

    34

    UniProt

    P11310
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