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    2. 最近搜索:細胞培養 微生物學 分子生物 生物化學
      首頁>>免疫學>>一抗>>NADH脫氫酶黃素蛋白1抗體
      NADH脫氫酶黃素蛋白1抗體
      • 產品貨號:
        BN40985R
      • 中文名稱:
        NADH脫氫酶黃素蛋白1抗體
      • 英文名稱:
        Rabbit anti-NDUFV1 Polyclonal antibody
      • 品牌:
        Biorigin
      • 貨號

        產品規格

        售價

        備注

      • BN40985R-100ul

        100ul

        ¥2360.00

        交叉反應:Human,Mouse,Rat(predicted:Dog,Pig,Cow,Horse) 推薦應用:WB,IHC-P,IHC-F,IF,ELISA

      • BN40985R-200ul

        200ul

        ¥3490.00

        交叉反應:Human,Mouse,Rat(predicted:Dog,Pig,Cow,Horse) 推薦應用:WB,IHC-P,IHC-F,IF,ELISA

      產品描述

      英文名稱NDUFV1
      中文名稱NADH脫氫酶黃素蛋白1抗體
      別    名CI 51kD; Complex I 51kD; NADH dehydrogenase (ubiquinone) flavoprotein 1; NADH dehydrogenase [ubiquinone] flavoprotein 1, mitochondrial; NADH dehydrogenase flavoprotein 1; NADH ubiquinone oxidoreductase 51 kDa subunit; NADH ubiquinone oxidoreductase; NDUFV 1; UQOR1; NDUV1_HUMAN.  
      研究領域腫瘤  細胞生物  免疫學  線粒體  
      抗體來源Rabbit
      克隆類型Polyclonal
      交叉反應Human, Mouse, Rat,  (predicted: Dog, Pig, Cow, Horse, )
      產品應用WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:100-500 (石蠟切片需做抗原修復)
      not yet tested in other applications.
      optimal dilutions/concentrations should be determined by the end user.
      分 子 量49kDa
      細胞定位細胞漿 細胞膜 線粒體
      性    狀Liquid
      濃    度1mg/ml
      免 疫 原KLH conjugated synthetic peptide derived from human NDUFV1:41-140/464 
      亞    型IgG
      純化方法affinity purified by Protein A
      儲 存 液0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
      保存條件Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
      PubMedPubMed
      產品介紹The mitochondrial respiratory chain provides energy to cells via oxidative phosphorylation and consists of four membrane-bound electron-transporting protein complexes (I-IV) and an ATP synthase (complex V). This gene encodes a 51 kDa subunit of the NADH:ubiquinone oxidoreductase complex I; a large complex with at least 45 nuclear and mitochondrial encoded subunits that liberates electrons from NADH and channels them to ubiquinone. This subunit carries the NADH-binding site as well as flavin mononucleotide (FMN)- and Fe-S-biding sites. Defects in complex I are a common cause of mitochondrial dysfunction; a syndrome that occurs in approximately 1 in 10,000 live births. Mitochondrial complex I deficiency is linked to myopathies, encephalomyopathies, and neurodegenerative disorders such as Parkinson's disease and Leigh syndrome. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009]

      Function:
      Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone (By similarity).

      Subunit:
      Complex I is composed of 45 different subunits. This is a component of the flavoprotein-sulfur (FP) fragment of the enzyme.

      Subcellular Location:
      Mitochondrion inner membrane; Peripheral membrane protein; Matrix side.

      DISEASE:
      Defects in NDUFV1 are a cause of Leigh syndrome (LS) [MIM:256000]. LS is a severe neurological disorder characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions.

      Similarity:
      Belongs to the complex I 51 kDa subunit family.

      SWISS:
      P49821

      Gene ID:
      4723

      Database links:

      Entrez Gene: 287014 Cow

      Entrez Gene: 4723 Human

      Entrez Gene: 17995 Mouse

      Entrez Gene: 293655 Rat

      Omim: 161015 Human

      SwissProt: P25708 Cow

      SwissProt: P49821 Human

      SwissProt: Q91YT0 Mouse

      SwissProt: Q5XIH3 Rat

      Unigene: 7744 Human

      Unigene: 29842 Mouse



      Important Note:
      This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic application

















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