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SURF-1 Polyclonal Antibody
SURF-1 Polyclonal Antibody
SURF-1 Polyclonal Antibody
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商品属性

Target:SURF-1

Gene Name:SURF1

Protein Name:Surfeit locus protein 1

Human Gene Id:6834

Human Swiss Prot No:Q15526

Mouse Gene Id:20930

Mouse Swiss Prot No:P09925

Rat Gene Id:64463

Rat Swiss Prot No:Q9QXU2

Immunogen:The antiserum was produced against synthesized peptide derived from human SURF1. AA range:171-220

Specificity:SURF-1 Polyclonal Antibody detects endogenous levels of SURF-1 protein.

Formulation:Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Source:Polyclonal, Rabbit,IgG

Dilution:WB 1:500 - 1:2000. IHC 1:100 - 1:300. IF 1:200 - 1:1000. ELISA: 1:20000. Not yet tested in other applications.

Purification:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration:1 mg/ml

Storage Stability:-15°C to -25°C/1 year(Do not lower than -25°C)

Other Name:SURF1;SURF-1;Surfeit locus protein 1

Observed Band(KD):30kD

Background: 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],

Function: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.,

Subcellular Location:Mitochondrion inner membrane ; Multi-pass membrane protein .

Expression: Colon,Kidney,Skin,Stomach,

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