Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 8 (ERCC8) (N-Term) Peptid
ERCC8
Reaktivität: Human, Maus
Wirt: Synthetic
BP, WB
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- Target Alle ERCC8 Produkte
- ERCC8 (Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 8 (ERCC8))
- Protein Region
- N-Term
- Spezies
- Human, Maus
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Quelle
- Synthetic
- Applikation
- Blocking Peptide (BP), Western Blotting (WB)
- Produktmerkmale
- This is a synthetic peptide designed for use in combination with anti-ERCC8 antibody (Catalog #: ARP57955_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Aufreinigung
- Purified
-
-
- Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Lyophilized
- Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Konzentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handhabung
- Avoid repeated freeze-thaw cycles.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- ERCC8 (Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 8 (ERCC8))
- Synonyme
- 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
- Hintergrund
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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).This gene encodes 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). CS cells are abnormally sensitive to ultraviolet radiation and are defective in the repair of transcriptionally active genes.
Alias Symbols: CKN1, CSA
Protein Interaction Partner: CBR1,DDB1,ERCC6,GTF2H2,UQCRQ,XAB2,COPS5,COPS6,CUL4A,CUL4B,DDB1,XAB2
Protein Size: 396 - Molekulargewicht
- 44 kDa
- Gen-ID
- 1161
- NCBI Accession
- NM_000082, NP_000073
- UniProt
- B2RB64
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