Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 8 (ERCC8) (Middle Region) Peptide
ERCC8
Reactivité: Humain
Hôte: Synthetic
BP, WB
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- Antigène Tous les produits ERCC8
- ERCC8 (Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 8 (ERCC8))
- Protein Region
- Middle Region
- Origine
- Humain
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Source
- Synthetic
- Application
- Blocking Peptide (BP), Western Blotting (WB)
- Séquence
- FQELYSGSRD CNILAWVPSL YEPVPDDDET TTKSQLNPAF EDAWSSSDEE
- Attributs du produit
- This is a synthetic peptide designed for use in combination with anti-ERCC8 Antibody(ARP58571_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.
- Purification
- Purified
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- Indications d'application
- Each Investigator should determine their own optimal working dilution for specific applications.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Concentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Conseil sur la manipulation
- Avoid repeated freeze-thaw cycles.
- Stock
- -20 °C
- Stockage commentaire
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Antigène
- ERCC8 (Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 8 (ERCC8))
- Synonymes
- 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
- Sujet
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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).
Alias Symbols: CKN1, CSA
Protein Interaction Partner: CBR1,DDB1,ERCC6,GTF2H2,UQCRQ,XAB2,COPS5,COPS6,CUL4A,CUL4B,DDB1,XAB2
Protein Size: 396 - Poids moléculaire
- 44 kDa
- ID gène
- 1161
- NCBI Accession
- NM_000082, NP_000073
- UniProt
- Q13216
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