ERCC6 Rekombinanter Antikörper
ERCC6 Rekombinant Antikörper für WB, Indirect ELISA
Wirt / Isotyp
Kaninchen / IgG
Getestete Reaktivität
human
Anwendung
WB, Indirect ELISA
Konjugation
Unkonjugiert
CloneNo.
250645D4
Kat-Nr. : 86144-1-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
86144-1-PBS bindet in WB, Indirect ELISA ERCC6 und zeigt Reaktivität mit human
| Getestete Reaktivität | human |
| Wirt / Isotyp | Kaninchen / IgG |
| Klonalität | Rekombinant |
| Typ | Antikörper |
| Immunogen | ERCC6 fusion protein Ag18009 |
| Vollständiger Name | excision repair cross-complementing rodent repair deficiency, complementation group 6 |
| Berechnetes Molekulargewicht | 1493 aa, 168 kDa |
| Beobachtetes Molekulargewicht | 180 kDa |
| GenBank-Zugangsnummer | BC127104 |
| Gene symbol | ERCC6/CSB |
| Gene ID (NCBI) | 2074 |
| Konjugation | Unkonjugiert |
| Form | Liquid |
| Reinigungsmethode | Protein-A-Reinigung |
| Lagerungspuffer | PBS only |
| Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
ERCC6, also named as CSB, belongs to the SNF2/RAD54 helicase family. It is involved in the preferential repair of active genes. It is presumed DNA or RNA unwinding function. ERCC6 corrects the UV survival and RNA synthesis after UV exposure of Cockayne syndrome complementation group B. Defects in ERCC6 are the cause of Cockayne syndrome type B (CSB) , cerebro-oculo-facio-skeletal syndrome type 1 (COFS1), De Sanctis-Cacchione syndrome (DSC), and UV-sensitive syndrome (UVS). Genetic variation in ERCC6 is associated with susceptibility to age-related macular degeneration type 5 (ARMD5). The antibody is specific to ERCC6.

