Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 8 (ERCC8) Peptide
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- Target See all ERCC8 products
- ERCC8 (Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 8 (ERCC8))
- Peptide Type
- Synthetic
- Origin
- Mammalian
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
- Sequence
- FQELYSGSRD CNILAWVPSL YEPVPDDDET TTKSQLNPAF EDAWSSSDEE
- Characteristics
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A synthetic peptide for use as a blocking control in assays to test for specificity of ERCC8 antibody,
Alternative Names: ERCC8 control peptide, ERCC8 antibody Blocking Peptide, Anti-ERCC8 Blocking Peptide, Excision Repair Cross-Complementing Rodent Repair Deficiency Complementation Group 8 Blocking Peptide, CKN1 Blocking Peptide, CSA Blocking Peptide - Purification
- Prepared from rabbit serum by affinity purification via sequential chromatography on phospho- and dephosphopeptide affinity columns.
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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
- ERCC8 (Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 8 (ERCC8))
- Synonyms
- zgc:103550 Peptide, CKN1 Peptide, CSA Peptide, UVSS2 Peptide, Ckn1 Peptide, 2410022P04Rik Peptide, 2810431L23Rik Peptide, 4631412O06Rik Peptide, B130065P18Rik Peptide, Csa Peptide, excision repair cross-complementation group 8 Peptide, ERCC excision repair 8, CSA ubiquitin ligase complex subunit Peptide, excision repaiross-complementing rodent repair deficiency, complementation group 8 Peptide, ercc8 Peptide, ERCC8 Peptide, Ercc8 Peptide
- Background
- ERCC8 is a WD repeat protein, which interacts with Cockayne syndrome type B (CSB) protein and with p44 protein, a subunit of the RNA polymerase II transcription factor IIH. Mutations in this gene have been identified in patients with hereditary disease Cockayne syndrome (CS).
- Molecular Weight
- 44 kDa
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