SCO1 Antibody, FITC conjugated
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中文名稱：SCO1兔多克隆抗體, FITC偶聯
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貨號：CSB-PA020852LC01HU
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規格：￥880
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其他：
產品詳情
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產品名稱：Rabbit anti-Homo sapiens (Human) SCO1 Polyclonal antibody
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Uniprot No.：
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基因名：SCO1
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別名：Cytochrome oxidase deficient homolog antibody; Cytochrome oxidase deficient homolog 1 antibody; Protein SCO1 homolog mitochondrial antibody; Protein SCO1 homolog, mitochondrial antibody; SCO (cytochrome oxidase deficient yeast) homolog 1 antibody; SCO cytochrome oxidase deficient homolog 1 (yeast) antibody; SCO cytochrome oxidase deficient homolog 1 antibody; sco1 antibody; SCO1_HUMAN antibody; SCOD1 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 Protein SCO1 homolog, mitochondrial protein (29-176AA)
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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.
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用途：For Research Use Only. Not for use in diagnostic or therapeutic procedures.
產品評價
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靶點詳情
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功能：Copper metallochaperone essential for the maturation of cytochrome c oxidase subunit II (MT-CO2/COX2). Not required for the synthesis of MT-CO2/COX2 but plays a crucial role in stabilizing MT-CO2/COX2 during its subsequent maturation. Involved in transporting copper to the Cu(A) site on MT-CO2/COX2. Plays an important role in the regulation of copper homeostasis by controlling the abundance and cell membrane localization of copper transporter CTR1.
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基因功能參考文獻：
- Results find that COA6 associates with COX2 and is crucial for its maturation and complex IV biogenesis. Also, COA6 interacts with the copper chaperone SCO1 which indicates that COA6 is intrinsically involved in the copper delivery process for COX2. PMID: 26160915
- Sco1 is a metallochaperone that selectively transfers Cu(I) ions based on loop recognition, whereas Sco2 is a copper-dependent thiol reductase of the cysteine ligands in the oxidase. PMID: 26351686
- COX20 cooperates with SCO1 and SCO2 to mature COX2 and promote the assembly of cytochrome c oxidase. PMID: 24403053
- COX19 is necessary for the transduction of a SCO1-dependent mitochondrial redox signal that regulates ATP7A-mediated cellular copper efflux. PMID: 23345593
- Results describe the tissue distribution of SCO1 and SCO2 in mouse and human tissues. PMID: 20864674
- SCO1 facilitates the transfer of copper from SCO2 to the CuA site at an early stage of COX assembly in mitochondria. PMID: 15229189
- data suggest that both Cu(I) and Cu(II) binding are critical for normal Sco function. PMID: 16091356
- Cox17-mediated copper metallation of Sco1, as well as the subsequent failure of Cu(A) site maturation, is the basis for the inefficient assembly of the cytochrome c oxidase complex in SCO1 patients PMID: 16520371
- Sco1 has evolved to bind a metal atom via the di-Cys motif to act as a copper chaperone, the oxidized form of the nickel-bound protein suggests that it may also maintain the thioredoxin function. PMID: 16735468
- These results suggest a mitochondrial pathway for the regulation of cellular copper content that involves signaling through SCO1 and SCO2, perhaps by their thiol redox or metal-binding state. PMID: 17189203
- Cu(I)HCox17(2S-S), i.e., the copper-loaded form of the protein, can transfer simultaneously copper(I) and two electrons to the human cochaperone Sco1 (HSco1) in the oxidized state, i.e., with its metal-binding cysteines forming a disulfide bond. PMID: 18458339
- a fraction of Sco1 physically associates with the cytochrome c oxidase complex in human muscle mitochondria, suggesting a possible direct relationship between CcO and the regulation of cellular copper homeostasis PMID: 19295170
- SCO2 acts upstream of SCO1, and that it is indispensable for CO II synthesis. PMID: 19336478
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相關疾病：Mitochondrial complex IV deficiency (MT-C4D)
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亞細胞定位：Mitochondrion. Mitochondrion inner membrane; Single-pass membrane protein.
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蛋白家族：SCO1/2 family
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組織特異性：Predominantly expressed in tissues characterized by high rates of oxidative phosphorylation (OxPhos), including muscle, heart, and brain.
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數據庫鏈接：
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