NDUFB3 Antibody, FITC conjugated
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中文名稱:NDUFB3兔多克隆抗體, FITC偶聯(lián)
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貨號:CSB-PA015645LC01HU
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規(guī)格:¥880
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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) NDUFB3 Polyclonal antibody
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Uniprot No.:
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基因名:
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別名:NDUFB3; NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 3; Complex I-B12; CI-B12; NADH-ubiquinone oxidoreductase B12 subunit
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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] 1 beta subcomplex subunit 3 protein (2-65AA)
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免疫原種屬:Homo sapiens (Human)
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標記方式:FITC
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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:>95%, Protein G 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:Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, pH 7.4 -
產(chǎn)品提供形式:Liquid
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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.
相關產(chǎn)品
靶點詳情
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功能:Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed not to be involved in 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.
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基因功能參考文獻:
- Recessive mutations in NDUFB3 cause complex I deficiency PMID: 22277967
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相關疾病:Mitochondrial complex I deficiency (MT-C1D)
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亞細胞定位:Mitochondrion inner membrane; Single-pass membrane protein; Matrix side.
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蛋白家族:Complex I NDUFB3 subunit family
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數(shù)據(jù)庫鏈接:
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