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SCCD Rabbit pAb (bs-8848R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包裝/詢價(jià)
產(chǎn)品編號(hào) bs-8848R
英文名稱 SCCD Rabbit pAb
中文名稱 抑癌蛋白UBIAD1抗體
別    名 UBIAD1; RP4-796F18.1; SCCD; TERE 1; tere1; Transitional epithelia response protein; Transitional epithelial response protein 1; UbiA prenyltransferase domain containing 1; UbiA prenyltransferase domain containing protein 1; UbiA prenyltransferase domain-c  
研究領(lǐng)域 腫瘤  細(xì)胞生物  
抗體來源 Rabbit
克隆類型 Polyclonal
交叉反應(yīng) (predicted: Human,Mouse,Rat,Pig,Sheep,Cow,Horse)
產(chǎn)品應(yīng)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 37 kDa
檢測(cè)分子量
細(xì)胞定位 細(xì)胞核 細(xì)胞漿 
性    狀 Liquid
濃    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human SCCD: 2-100/338 
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(xiàng) 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 protein thought to be involved in cholesterol and phospholipid metabolism. Mutations in this gene are associated with Schnyder crystalline corneal dystrophy. [provided by RefSeq, Oct 2008]

Function:
Prenyltransferase that mediates the formation of menaquinone-4 (MK-4) and coenzyme Q10. MK-4 is a vitamin K2 isoform present at high concentrations in the brain, kidney and pancreas, and is required for endothelial cell development. Mediates the conversion of phylloquinone (PK) into MK-4, probably by cleaving the side chain of phylloquinone (PK) to release 2-methyl-1,4-naphthoquinone (menadione; K3) and then prenylating it with geranylgeranyl pyrophosphate (GGPP) to form MK-4. Also plays a role in cardiovascular development independently of MK-4 biosynthesis, by acting as a coenzyme Q10 biosyntetic enzyme: coenzyme Q10, also named ubiquinone, plays a important antioxidant role in the cardiovascular system. Mediates biosynthesis of coenzyme Q10 in the Golgi membrane, leading to protect cardiovascular tissues from NOS3/eNOS-dependent oxidative stress.

Subcellular Location:
Endoplasmic reticulum membrane. Cytoplasm. Nucleus. Mitochondrion.

Tissue Specificity:
Ubiquitously expressed.

DISEASE:
Defects in UBIAD1 are the cause of crystalline corneal dystrophy of Schnyder (SCCD) [MIM:121800]. SCCD is a rare autosomal dominant disease characterized by progressive corneal opacification resulting from abnormal deposition of cholesterol and phospholipids.

Similarity:
Belongs to the ubiA prenyltransferase family.

SWISS:
Q9Y5Z9

Gene ID:
29914

Database links:

Entrez Gene: 29914 Human

Entrez Gene: 71707 Mouse

Entrez Gene: 313706 Rat

Omim: 611632 Human

SwissProt: Q9Y5Z9 Human

SwissProt: Q9DC60 Mouse

SwissProt: D3ZG27 Rat

Unigene: 522933 Human

Unigene: 292503 Mouse

Unigene: 203344 Rat



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