DHODH Antibody, HRP conjugated
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								中文名稱:DHODH兔多克隆抗體, HRP偶聯(lián)
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								貨號(hào):CSB-PA006852LB01HU
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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) DHODH Polyclonal antibody
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											Uniprot No.:
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											基因名:DHODH
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											別名:DHOdehase antibody; Dhodh antibody; Dihydroorotate dehydrogenase (quinone) antibody; Dihydroorotate dehydrogenase antibody; Dihydroorotate dehydrogenase mitochondrial antibody; Dihydroorotate oxidase antibody; Human complement of yeast URA1 antibody; mitochondrial antibody; POADS antibody; PYRD_HUMAN antibody; URA1 antibody
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											宿主:Rabbit
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											反應(yīng)種屬:Human
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											免疫原:Recombinant Human Dihydroorotate dehydrogenase (quinone), mitochondrial protein (241-395AA)
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											免疫原種屬:Homo sapiens (Human)
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											標(biāo)記方式:HRP
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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
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											產(chǎn)品提供形式:Liquid
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											應(yīng)用范圍:ELISA
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											Protocols:
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											儲(chǔ)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.
相關(guān)產(chǎn)品
靶點(diǎn)詳情
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											功能:Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor.
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											基因功能參考文獻(xiàn):- This case with grossly raised plasma DHO represents the first biochemical confirmation of functional DHODH deficiency. DHO was also easily detectable in dried plasma and blood spots. PMID: 27370710
- This is the first study to report on conformational changes of the HsDHODH N-terminal microdomain through a combination of CD and DEER spectroscopic techniques PMID: 26086954
- Considering that pyrimidine deficiency alone does not induce craniofacial dysmorphism, the DHODH mutations may contribute to the Miller syndrome in part through somehow altered mitochondrial function. PMID: 23216091
- Carriage of a six-marker DHODH haplotype was associated with a reduced treatment response (p = 0.008). PMID: 22966891
- The G202A and R346W mutation causes deficient protein stability, and the R135C mutation impairs the substrate-induced enzymatic activity, suggesting that impairment of DHODH activity is linked to the Miller syndrome phenotype. PMID: 22967083
- biallelic DHODH mutations in four unrelated families with typical clinical features of Miller syndrome. PMID: 22692683
- DHODH inhibition led to a marked decrease in melanoma growth both in vitro and in xenograft studies PMID: 21430780
- DHODH recessively causes Miller syndrome. PMID: 20220176
- required for N-(4-hydroxyphenyl)retinamide-induced reactive oxygen species production and apoptosis of cancer epithelial cells PMID: 20399851
- Data confirmed the presence of DHODH mutations in families with Miller syndrome. PMID: 19915526
- biophysical analysis of hydrogen bonding pathways in human dihydroorotate dehydrogenase PMID: 17004840
- Data provide new insights into the dynamic features of the DHODH reaction and suggest new approaches to the design of inhibitors against DHODH. PMID: 18672895
- DHODH polymorphism may be associated with incireased remiaaion in leflunomide treatment in rheumatoid arthritis patients. PMID: 19207032
- we report a new association of DHODH A40C polymorphism with leflunomide toxicity in patients with Rheumatoid Arthritis. PMID: 19605743
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											相關(guān)疾病:Postaxial acrofacial dysostosis (POADS)
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											亞細(xì)胞定位:Mitochondrion inner membrane; Single-pass membrane protein.
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											蛋白家族:Dihydroorotate dehydrogenase family, Type 2 subfamily
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											數(shù)據(jù)庫鏈接:
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