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Arylsulfatase E Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT0349
产品名称
Arylsulfatase E Rabbit Polyclonal Antibody
别名
ARSE; Arylsulfatase E; ASE
类别
常规抗体
基因名称
ARSE
蛋白名称
Arylsulfatase E
推荐应用
WB
反应种属
Human,Rat,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
415
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=415
Human Swissprot No.
P51690
Human Swissprot Link
http://www.uniprot.org/uniprotkb/P51690/entry
免疫原
Synthesized peptide derived from Arylsulfatase E . at AA range: 120-200
特异性
Arylsulfatase E Polyclonal Antibody detects endogenous levels of Arylsulfatase E protein.
稀释度
WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.
预测分子量
65kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
Arylsulfatase E is a member of the sulfatase family. It is glycosylated postranslationally and localized to the golgi apparatus. Sulfatases are essential for the correct composition of bone and cartilage matrix. X-linked chondrodysplasia punctata, a disease characterized by abnormalities in cartilage and bone development, has been linked to mutations in this gene. Alternative splicing results in multiple transcript variants. A pseudogene related to this gene is located on the Y chromosome. [provided by RefSeq, Sep 2013],
组织表达
Expressed in the pancreas, liver and kidney.
细胞定位
Golgi apparatus, Golgi stack .
功能
cofactor:Binds 1 calcium ion per subunit.,disease:Defects in ARSE are the cause of chondrodysplasia punctata X-linked recessive type 1 (CDPX1) [MIM:302950]. CDP is a clinically and genetically heterogeneous disorder characterized by punctiform calcification of the bones. CDPX1 is a congenital defect of bone and cartilage development characterized by aberrant bone mineralization, severe underdevelopment of nasal cartilage, and distal phalangeal hypoplasia. This disease can also be induced by inhibition with the drug warfarin.,enzyme regulation:Inhibited by millimolar concentrations of warfarin.,function:May be essential for the correct composition of cartilage and bone matrix during development. Has no activity toward steroid sulfates.,PTM:N-glycosylated.,PTM:The conversion to 3-oxoalanine (also known as C-formylglycine, FGly), of a serine or cysteine residue in prokaryotes and of a cysteine residue in eukaryotes, is critical for catalytic activity.,similarity:Belongs to the sulfatase family.,tissue specificity:Expressed in the pancreas, liver and kidney.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Western blot analysis of mouse-brain HELA SH-SY5Y lysis using Arylsulfatase E antibody. Antibody was diluted at 1:1000

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