Surfeit 1 (SURF1) Peptide
SURF1
Reactivity: Mammalian
Host: Synthetic
BP, WB, IHC
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- Target See all SURF1 products
- SURF1 (Surfeit 1 (SURF1))
- Peptide Type
- Synthetic
- Origin
- Mammalian
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Sequence
- GLRAAGLGRA PASAAWRSVL RVSPRPGVAW RPSRCGSSAA EASATKAEDD
- Characteristics
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A synthetic peptide for use as a blocking control in assays to test for specificity of SURF1 antibody,
Alternative Names: SURF1 control peptide, SURF1 antibody Blocking Peptide, Anti-SURF1 Blocking Peptide, surfeit 1 Blocking Peptide, SURF1, SURF-1, SURF 1, SURF-1 Blocking Peptide, SURF 1 Blocking Peptide
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- Application Notes
- Optimal conditions should be determined by the investigator
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.
- Buffer
- PBS
- Handling Advice
- Avoid repeated freeze/thaw cycles.
- Storage
- -20 °C
- Storage Comment
- Store at -20 °C long term.
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- Target
- SURF1 (Surfeit 1 (SURF1))
- Synonyms
- BcDNA:GH23574 Peptide, CG9943 Peptide, Dmel\\CG9943 Peptide, GB14201 Peptide, SURF1 Peptide, im:6898613 Peptide, zgc:158646 Peptide, Ab1-205 Peptide, SURF-1 Peptide, 0610010F23Rik Peptide, Surf-1 Peptide, SURFEIT 1 Peptide, Surfeit 1 Peptide, surfeit locus protein 1 Peptide, SURF1, cytochrome c oxidase assembly factor Peptide, surfeit 1 Peptide, surfeit gene 1 Peptide, Surfeit locus 1 cytochrome c oxidase biogenesis protein Peptide, Surf1 Peptide, LOC413781 Peptide, SURF1 Peptide, surf1 Peptide
- 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.
- Molecular Weight
- 33 kDa
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