NDUFS7 Antibody
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中文名稱：NDUFS7兔多克隆抗體
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貨號：CSB-PA015666ESR1HU
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規(guī)格：￥440
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其他：
產(chǎn)品詳情
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產(chǎn)品名稱：Rabbit anti-Homo sapiens (Human) NDUFS7 Polyclonal antibody
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Uniprot No.：
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基因名：
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別名：CI 20 antibody; CI-20kD antibody; Complex I 20kDa subunit antibody; Complex I mitochondrial respiratory chain 20 KD subunit antibody; Complex I-20kD antibody; FLJ45860 antibody; FLJ46880 antibody; MGC120002 antibody; MY017 antibody; NADH coenzyme Q reductase antibody; NADH dehydrogenase (ubiquinone) Fe S protein 7 20kDa (NADH coenzyme Q reductase) antibody; NADH dehydrogenase (ubiquinone) FeS protein 7; 20kDa (NADHcoenzyme Q reductase) antibody; NADH dehydrogenase (ubiquinone) FeS protein7; 20kDa (NADHcoenzyme Q reductase) antibody; NADH dehydrogenase [ubiquinone] iron-sulfur protein 7; mitochondrial antibody; NADH-ubiquinone oxidoreductase 20 kDa subunit antibody; NADH:ubiquinone oxidoreductase PSST subunit antibody; NADHcoenzyme Q reductase antibody; Ndufs7 antibody; NDUS7_HUMAN antibody; PSST antibody; PSST subunit antibody
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宿主：Rabbit
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反應種屬：Human
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免疫原：Recombinant Human NADH dehydrogenase [ubiquinone] iron-sulfur protein 7, mitochondrial protein (39-213AA)
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免疫原種屬：Homo sapiens (Human)
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標記方式：Non-conjugated
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克隆類型：Polyclonal
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抗體亞型：IgG
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純化方式：Antigen Affinity Purified
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濃度：It differs from different batches. Please contact us to confirm it.
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保存緩沖液：PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
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產(chǎn)品提供形式：Liquid
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應用范圍：ELISA
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Protocols：
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儲存條件：Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期：Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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用途：For Research Use Only. Not for use in diagnostic or therapeutic procedures.
產(chǎn)品評價
相關(guān)產(chǎn)品
靶點詳情
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功能：Core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) which catalyzes electron transfer from NADH through the respiratory chain, using ubiquinone as an electron acceptor. Essential for the catalytic activity of complex I.
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基因功能參考文獻：
- However, similar to another family member, RdmB, it catalyzes the introduction of a hydroxyl group, in the case of NDUFAF5, into Arg-73 in the NDUFS7 subunit of human complex I PMID: 27226634
- no active role of NDUFS7 gene in schizophrenia, was found. PMID: 22935918
- Observational study of gene-disease association. (HuGE Navigator) PMID: 20877624
- A patient with Leigh syndrome (LS), born to consanguineous parents, with severe complex I defect and a novel mutation in the NDUFS7 gene subunit. PMID: 17275378
- Intronic NDUFS7 gene mutation is associated with activation of a cryptic exon and impaired assembly of mitochondrial complex I in a patient with Leigh syndrome PMID: 17604671
- Both the amount and intrinsic activity of complex I are decreased in inherited complex I deficiency, ehich can be increased by Trolox. PMID: 18435906
- Observational study of gene-disease association. (HuGE Navigator) PMID: 17601350
- Observational study of gene-disease association. (HuGE Navigator) PMID: 18977241
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相關(guān)疾病：Leigh syndrome (LS); Mitochondrial complex I deficiency (MT-C1D)
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亞細胞定位：Mitochondrion inner membrane; Peripheral membrane protein; Matrix side.
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蛋白家族：Complex I 20 kDa subunit family
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數(shù)據(jù)庫鏈接：
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