SCO2 Antibody

說明書

中文名稱：

SCO2兔多克隆抗體
貨號：

CSB-PA020853ESR2HU
規(guī)格：

￥440
圖片：
Immunohistochemistry of paraffin-embedded human adrenal gland tissue using CSB-PA020853ESR2HU at dilution of 1:100

Immunohistochemistry of paraffin-embedded human gastric cancer using CSB-PA020853ESR2HU at dilution of 1:100
其他：

產(chǎn)品詳情
產(chǎn)品評價
相關(guān)產(chǎn)品
靶點詳情

產(chǎn)品詳情

產(chǎn)品名稱：

Rabbit anti-Homo sapiens (Human) SCO2 Polyclonal antibody
Uniprot No.：

O43819
基因名：

SCO2
別名：

Cytochrome oxidase deficient homolog 2 antibody; MGC125823 antibody; MGC125825 antibody; OTTHUMP00000196774 antibody; OTTHUMP00000196775 antibody; Protein SCO2 homolog; mitochondrial antibody; SCO (cytochrome oxidase deficient; yeast) homolog 2 antibody; SCO 1L antibody; SCO 2 antibody; SCO cytochrome oxidase deficient homolog 2 (yeast) antibody; SCO cytochrome oxidase deficient homolog 2 antibody; SCO1L antibody; SCO2 antibody; SCO2_HUMAN antibody; Synthesis of cytochrome c oxidase 2 antibody
宿主：

Rabbit
反應(yīng)種屬：

Human
免疫原：

Recombinant Human Protein SCO2 homolog, mitochondrial protein (1-130AA)
免疫原種屬：

Homo sapiens (Human)
標(biāo)記方式：

Non-conjugated
克隆類型：

Polyclonal
抗體亞型：

IgG
純化方式：

Antigen Affinity Purified
濃度：

It differs from different batches. Please contact us to confirm it.
保存緩沖液：

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
產(chǎn)品提供形式：

Liquid
應(yīng)用范圍：

ELISA, IHC

推薦稀釋比：

Application	Recommended Dilution
IHC	1:20-1:200

Protocols：

ELISA Protocol
Immunohistochemistry (IHC) Protocol
儲存條件：

Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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.
用途：

For Research Use Only. Not for use in diagnostic or therapeutic procedures.

產(chǎn)品評價

靶點詳情

功能：

Copper metallochaperone essential for the synthesis and maturation of cytochrome c oxidase subunit II (MT-CO2/COX2). Involved in transporting copper to the Cu(A) site on MT-CO2/COX2. Also acts as a thiol-disulfide oxidoreductase to regulate the redox state of the cysteines in SCO1 during maturation of MT-CO2/COX2.
基因功能參考文獻(xiàn)：
1. We identified one novel possibility of an extreme myopia-causing mutation in SCO2. No other disease-causing mutation was found in 101 extremely myopic Japanese patients, suggesting that SCO2 plays a limited role in Japanese extreme myopia. PMID: 27052445
2. In gastric cancer, the expression of SCO2 and COX were not shown to be associated with the regulatory role of p53, unlike TIGAR expression. Nevertheless, a significantly high recurrence rate was found in a patient group with high COX expression PMID: 27499152
3. oxidative stress-induced glycolysis-to-OXPHOS switch is mediated by synthesis of cytochrome c oxidase 2 (SCO2). These findings demonstrate p53-mediated OXPHOS function as a compensatory alteration in Fanconi anemia (FA)hematopoietic stem cells to ensure a functional but mildly impaired energy metabolism and suggest a cautious approach to manipulating p53 signaling in FA. PMID: 26676373
4. Geranylgeranoic acid increased the SCO2 gene expression, which might enhance aerobic respiration. PMID: 26700591
5. oncoprotein HBXIP enhances glucose metabolism reprogramming through suppressing SCO2 and PDHA1 in breast cancer PMID: 26309161
6. Cooperation between COA6 and SCO2 in COX2 maturation during cytochrome c oxidase assembly links two mitochondrial cardiomyopathies. PMID: 25959673
7. 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
8. Letter/Case Report: SCO2 mutations resulting in Leigh disease revealed at autopsy. PMID: 25720770
9. mutation in LRPAP1 is associated with high myopia. Further studies are expected to evaluate the pathogenicity of the variants in CTSH, LEPREL1, ZNF644, SLC39A5, and SCO2. PMID: 25525168
10. COX20 cooperates with SCO1 and SCO2 to mature COX2 and promote the assembly of cytochrome c oxidase. PMID: 24403053
11. alpha-particle-induced bystander effect is regulated by p53 and its downstream SCO2 in the irradiated hepatoma cells PMID: 23786650
12. oroxylin A could increase protein and mRNA expression of TP53-induced glycolysis and apoptosis regulator (TIGAR) and synthesis of cytochrome c oxidase 2 (SCO2), which are the key metabolic modulators regulated by p53. PMID: 23612020
13. Autosomal recessive mutations in SCO2 are known to be associated with COX deficiency recognized as fatal infantile cardio-encephalomyopathy PMID: 23364397
14. Exogenous addition of the SCO2 gene to hypoxic cancer cells and hypoxic tumors induces apoptosis. PMID: 23319048
15. Mutations in SCO2 are associated with autosomal-dominant high-grade myopia. PMID: 23643385
16. Analysis of the mtDNA revealed that COX deficiency is caused by high levels of mtDNA deletions which accumulate with age in alzheimer disease. PMID: 21925769
17. wild-type p53 gene silencing reduced the expression of synthesis of cytochrome c oxidase 2 (SCO2), an effector necessary for respiratory chain function PMID: 22120717
18. These results suggest that p53 can modulate the metabolic pathways via the proteins SCO2 and TIGAR in human breast cancer. PMID: 21820150
19. Results describe the tissue distribution of SCO1 and SCO2 in mouse and human tissues. PMID: 20864674
20. Mutations of SCO2 gene should be considered as a possible cause of neurogenic skeletal muscle features (including SMA-like) in infants with encephalomyopathy even in the absence of heart involvement and COX deficit. PMID: 19879173
21. recombinant fusion L-Sco2 protein was successfully transduced into the mitochondria of primary fibroblasts derived from SCO2/COX deficient patient and facilitated recovery of COX activity PMID: 20193760
22. Mutations can cause fatal cytochrome c oxidase deficiency. Affected myoblasts can be rescued in vitro by transduction of the normal SCO2 gene or by copper administration. PMID: 11751685
23. Copper supplementation restores cytochrome c oxidase activity in cultured cells from patients with SCO2 mutations. PMID: 11931660
24. One novel SCO2 mutation has been identified in a patient with hypertrophic cardiomyopathy. PMID: 12538779
25. SCO2 mutation is associated spinal muscular atrophy type I phenotype PMID: 14994243
26. SCO2 transfers copper to the CuA site at an early stage of COX assembly in mitochondria. PMID: 15229189
27. The consequences of SCO2 and SURF1 mutations suggest the existence of tissue-specific functional differences of these proteins that may serve different tissue-specific requirements for the regulation of COX biogenesis. PMID: 16083427
28. data suggest that both Cu(I) and Cu(II) binding are critical for normal Sco function. PMID: 16091356
29. findings show that p53 modulates the balance between the utilization of respiratory and glycolytic pathways; identifed Synthesis of Cytochrome c Oxidase 2 (SCO2) as the downstream mediator of this effect PMID: 16728594
30. 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
31. structural and metal binding features of human Cu(I)Sco2 are similar to the Sco1 homolog, although the dynamic properties and the conformational disorder are quite different when apo forms and the copper(I)-loaded forms of the two proteins are compared PMID: 17850752
32. report extends knowledge of the pathology of COX deficiency caused by mutations in the SCO2 gene PMID: 18254779
33. Spinal muscular atrophy has been associated with mtDNA depletion or with mutations in the cytochrome-c oxidase assembly gene (SCO2; OMIM 604377). PMID: 18332255
34. Mutations in the SCO2 gene are a cause of prenatal-onset hypertrophic cardiomyopathy. PMID: 18924171
35. SCO2 acts upstream of SCO1, and that it is indispensable for CO II synthesis. PMID: 19336478
36. observations confirm that mutations in the SCO2 gene are frequently associated with the neurogenic pattern of skeletal muscle involvement accompanied by mitochondrial abnormalities PMID: 19353431
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相關(guān)疾病：

Cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1 (CEMCOX1); Myopia 6 (MYP6); Leigh syndrome (LS)
亞細(xì)胞定位：

Mitochondrion inner membrane; Single-pass membrane protein.
蛋白家族：

SCO1/2 family
組織特異性：

Ubiquitous.
數(shù)據(jù)庫鏈接：

HGNC: 10604

OMIM: 256000

KEGG: hsa:9997

STRING: 9606.ENSP00000252785

UniGene: Hs.180903

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