ERCC5 antibody - N-terminal region
Produktgrößen
25ul
£177,00
ARP54287-P050-25UL
100 ul
£412,00
ARP54287-P050-100UL
Über dieses Produkt
- SKU:
- ARP54287-P050
- Zusätzliche Namen:
- XPG; UVDR; XPGC; COFS3; ERCM2; ERCC5-201
- Klonalität:
- Polyclonal
- Konzentration:
- 0.5 mg/ml
- Weitere Details:
- Excision repair cross-complementing rodent repair deficiency; complementation group 5 (xeroderma pigmentosum; complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome; which is characterized by severe growth defects; mental retardation; and cachexia. Excision repair cross-complementing rodent repair deficiency; complementation group 5 (xeroderma pigmentosum; complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome; which is characterized by severe growth defects; mental retardation; and cachexia. Multiple alternatively spliced transcript variants encoding distinct isoforms have been described; but the biological validity of all variants has not been determined. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
- Gendetails:
- Excision repair cross-complementing rodent repair deficiency; complementation group 5
- Host:
- Rabbit
- Immunogen:
- The immunogen is a synthetic peptide directed towards the N terminal region of human ERCC5
- Molekulargewicht:
- 133kDa
- Proteindetails:
- DNA repair protein complementing XP-G cells
- Aufreinigung:
- Affinity Purified
- Versandbedingungen:
- Blue Ice
- Lagerbedingungen:
- For short term use; store at 2-8C up to 1 week. For long term storage; store at -20C in small aliquots to prevent freeze-thaw cycles.
- Hersteller:
- Aviva Systems Biology
- Typ:
- Antibodies: Polyclonal Antibody
- Datenblatt des Herstellers:html_datasheet.php