SURF1 antibody (AA 140-220)
Quick Overview for SURF1 antibody (AA 140-220) (ABIN7217168)
Target
See all SURF1 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- AA 140-220
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Purpose
- SURF-1 Polyclonal Antibody
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Specificity
- SURF-1 Polyclonal Antibody detects endogenous levels of SURF-1 protein.
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Purification
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen
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Immunogen
- Synthesized peptide derived from the Internal region of human SURF-1 at AA range: 140-220
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Isotype
- IgG
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB (1:500-1:2000), IHC-P (1:100-1:300), IF (1:200-1:1000), ELISA (1:20000). Not yet tested in other applications.
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Comment
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Primary Antibody
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1 mg/mL
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Buffer
- PBS containing 50 % Glycerol, 0.5 % BSA and 0.02 % Sodium Azide.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- -20 °C
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Storage Comment
- Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
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- SURF1 (Surfeit 1 (SURF1))
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Alternative Name
- SURF-1
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Background
- Rabbit Anti-SURF-1 Polyclonal Antibody,SURF1, SURF-1, Surfeit locus protein 1,SURF1 encodes surfeit locus protein 1 localized to the inner mitochondrial membrane and thought to be involved in the biogenesis of the cytochrome c oxidase complex. Surfeit locus protein 1 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.,Surfeit locus protein 1
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Molecular Weight
- observerd band 30kDa
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Gene ID
- 6834
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UniProt
- Q15526
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Pathways
- Proton Transport, Ribonucleoside Biosynthetic Process
Target
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