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    DHODH Rabbit pAb (bs-14305R)  
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    50ul/1180.00元
    100ul/1980.00元
    200ul/2800.00元
    大包裝/詢價
    產品編號 bs-14305R
    英文名稱 DHODH Rabbit pAb
    中文名稱 二氫乳清酸脫氫酶抗體
    別    名 DHOdehase; Dhodh; Dihydroorotate dehydrogenase(quinone); Dihydroorotate dehydrogenase; Dihydroorotate dehydrogenase mitochondrial; Dihydroorotate oxidase; Human complement of yeast URA1; mitochondrial; PYRD_HUMAN.  
    研究領域 細胞生物  信號轉導  細胞骨架  
    抗體來源 Rabbit
    克隆類型 Polyclonal
    克 隆 號
    交叉反應 (predicted: Human,Mouse,Rat,Rabbit,Sheep,Cow,Dog,Horse)
    產品應用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500,ELISA=1:5000-10000
    not yet tested in other applications.
    optimal dilutions/concentrations should be determined by the end user.
    理論分子量 43 kDa
    檢測分子量
    細胞定位 細胞漿 
    性    狀 Liquid
    濃    度 1mg/ml
    免 疫 原 KLH conjugated synthetic peptide derived from human DHODH: 251-350/395 
    亞    型 IgG
    純化方法 affinity purified by Protein A
    緩 沖 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
    保存條件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
    注意事項 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
    PubMed PubMed
    產品介紹 The protein encoded by this gene catalyzes the fourth enzymatic step, the ubiquinone-mediated oxidation of dihydroorotate to orotate, in de novo pyrimidine biosynthesis. This protein is a mitochondrial protein located on the outer surface of the inner mitochondrial membrane. [provided by RefSeq, Jul 2008]

    Function:
    Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor.

    Subcellular Location:
    Mitochondrion inner membrane.

    Post-translational modifications:
    The uncleaved transit peptide is required for mitochondrial targeting and proper membrane integration.

    DISEASE:
    Defects in DHODH are the cause of postaxial acrofacial dysostosis (POADS) [MIM:263750]; also known as Miller syndrome. POADS is characterized by severe micrognathia, cleft lip and/or palate, hypoplasia or aplasia of the posterior elements of the limbs, coloboma of the eyelids and supernumerary nipples. POADS is a very rare disorder: only 2 multiplex families, each consisting of 2 affected siblings born to unaffected, nonconsanguineous parents, have been described among a total of around 30 reported cases.

    Similarity:
    Belongs to the dihydroorotate dehydrogenase family. Type 2 subfamily.

    SWISS:
    Q02127

    Gene ID:
    1723

    Database links:

    Entrez Gene: 1723 Human

    Entrez Gene: 533873 Cow

    Entrez Gene: 610755 Dog

    Entrez Gene: 56749 Mouse

    Entrez Gene: 65156 Rat

    Entrez Gene: 494065 Zebrafish

    Omim: 126064 Human

    SwissProt: Q02127 Human

    SwissProt: O35435 Mouse

    SwissProt: Q63707 Rat

    Unigene: 654427 Human

    Unigene: 23894 Mouse

    Unigene: 81502 Rat



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