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UMPS Rabbit pAb (bs-8110R)  
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產(chǎn)品編號 bs-8110R
英文名稱 UMPS Rabbit pAb
中文名稱 尿苷磷酸合成酶抗體
別    名 ODC; Uridine 5-monophosphate synthase; OMPdecase; OPRT; OPRTase; Orotate phosphoribosyl transferase and orotidine 5' decarboxylase; Orotate phosphoribosyltransferase; Orotate phosphoribosyltransferase phosphoribosyltransferase; Orotidine 5' phosphate decarboxylase; Orotidine 5''-phosphate decarboxylase; RP11-71H17.9; UMP synthase; Umps; UMPS_HUMAN; Uridine 5' monophosphate synthase; Uridine monophosphate synthetase.  
研究領(lǐng)域 細(xì)胞生物  信號轉(zhuǎn)導(dǎo)  表觀遺傳學(xué)  
抗體來源 Rabbit
克隆類型 Polyclonal
克 隆 號
交叉反應(yīng) Human (predicted: Mouse,Rat,Rabbit,Sheep,Cow,Dog,Horse, Cynomolgus Monkey,Rhesus monkey)
產(chǎn)品應(yīng)用 WB=1:500-2000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理論分子量 52 kDa
檢測分子量
細(xì)胞定位 細(xì)胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human UMPS: 351-450/480 
亞    型 IgG
純化方法 affinity purified by Protein A
緩 沖 液 Preservative: 0.02% Proclin300, Constituents: 1% BSA, 0.01M PBS, pH7.4.
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(chǎn)品介紹 This gene encodes a uridine 5'-monophosphate synthase. The encoded protein is a bifunctional enzyme that catalyzes the final two steps of the de novo pyrimidine biosynthetic pathway. The first reaction is carried out by the N-terminal enzyme orotate phosphoribosyltransferase which converts orotic acid to orotidine-5'-monophosphate. The terminal reaction is carried out by the C-terminal enzyme OMP decarboxylase which converts orotidine-5'-monophosphate to uridine monophosphate. Defects in this gene are the cause of hereditary orotic aciduria. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]

Subunit:
Homodimer.

DISEASE:
Defects in UMPS are the cause of orotic aciduria type 1 (ORAC1) [MIM:258900]. A disorder of pyrimidine metabolism resulting in megaloblastic anemia and orotic acid crystalluria that is frequently associated with some degree of physical and mental retardation. A minority of cases have additional features, particularly congenital malformations and immune deficiencies.

Similarity:
In the N-terminal section; belongs to the purine/pyrimidine phosphoribosyltransferase family.
In the C-terminal section; belongs to the OMP decarboxylase family.

SWISS:
P11172

Gene ID:
7372

Database links:

Entrez Gene: 460644 Chimpanzee

Entrez Gene: 101124432 Gorilla

Entrez Gene: 100070386 Horse

Entrez Gene: 7372 Human

Entrez Gene: 22247 Mouse

Entrez Gene: 100173867 Orangutan

Entrez Gene: 715664 Rhesus monkey

Omim: 613891 Human

SwissProt: P11172 Human

SwissProt: P13439 Mouse

SwissProt: Q5R514 Orangutan

Unigene: 2057 Human

Unigene: 13145 Mouse

Unigene: 466951 Mouse



產(chǎn)品圖片
Sample: Hela(Human)Cell Lysate at 40 ug 293T (Human) Cell Lysate at 40 ug Primary: Anti-UMPS(bs-8110R)at 1/300 dilution Secondary: IRDye800CW Goat Anti-RabbitIgG at 1/20000 dilution Predicted band size: 52kD Observed band size: 52kD
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