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SURF-1 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT4471
产品名称
SURF-1 Rabbit Polyclonal Antibody
别名
SURF1; SURF-1; Surfeit locus protein 1
类别
常规抗体
基因名称
SURF1
蛋白名称
Surfeit locus protein 1
推荐应用
WB
反应种属
Human,Mouse,Rat
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
6834
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6834
Human Swissprot No.
Q15526
Human Swissprot Link
http://www.uniprot.org/uniprotkb/Q15526/entry
Mouse Gene ID
20930
Mouse Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20930
Mouse Swissprot No.
P09925
Mouse Swissprot Link
http://www.uniprot.org/uniprot/P09925
Rat Gene ID
64463
Rat Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=64463
Rat Swissprot No.
Q9QXU2
Rat Swissprot Link
http://www.uniprot.org/uniprot/Q9QXU2
免疫原
The antiserum was produced against synthesized peptide derived from human SURF1. AA range:171-220
特异性
SURF-1 Polyclonal Antibody detects endogenous levels of SURF-1 protein.
稀释度
WB 1:500 - 1:2000. IHC 1:100 - 1:300. IF 1:200 - 1:1000. ELISA: 1:20000. Not yet tested in other applications.
预测分子量
30kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
This gene encodes a protein localized to the inner mitochondrial membrane and thought to be involved in the biogenesis of the cytochrome c oxidase complex. The protein is a member of the SURF1 family, which includes the related yeast protein SHY1 and rickettsial protein RP733. The gene is located in the surfeit gene cluster, a group of very tightly linked genes that do not share sequence similarity, where it shares a bidirectional promoter with SURF2 on the opposite strand. Defects in this gene are a cause of Leigh syndrome, a severe neurological disorder that is commonly associated with systemic cytochrome c oxidase deficiency. [provided by RefSeq, Jul 2008],
组织表达
Colon,Kidney,Skin,Stomach,
细胞定位
Mitochondrion inner membrane ; Multi-pass membrane protein .
功能
disease:Defects in SURF1 are a cause of Leigh syndrome (LS) [MIM:256000]. LS is a severe neurological disorder characterized by bilaterally symmetrical necrotic lesions in subcortical brain regions that is commonly associated with systemic cytochrome c oxidase (COX) deficiency.,function:Probably involved in the biogenesis of the COX complex.,similarity:Belongs to the SURF1 family.,
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 lysates from Jurkat cells, using SURF1 Antibody. The lane on the right is blocked with the synthesized peptide.

Western Blot analysis of various cells using SURF-1 Polyclonal Antibody

Western Blot analysis of Jurkat cells using SURF-1 Polyclonal Antibody

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