ESCO2 Polyklonaler Antikörper
ESCO2 Polyklonal Antikörper für WB, IHC, Indirect ELISA
Wirt / Isotyp
Kaninchen / IgG
Getestete Reaktivität
human, Maus, Ratte
Anwendung
WB, IHC, Indirect ELISA
Konjugation
Unkonjugiert
Kat-Nr. : 23525-1-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
23525-1-PBS bindet in WB, IHC, Indirect ELISA ESCO2 und zeigt Reaktivität mit human, Maus, Ratten
| Getestete Reaktivität | human, Maus, Ratte |
| Wirt / Isotyp | Kaninchen / IgG |
| Klonalität | Polyklonal |
| Typ | Antikörper |
| Immunogen | ESCO2 fusion protein Ag18893 |
| Vollständiger Name | establishment of cohesion 1 homolog 2 (S. cerevisiae) |
| Berechnetes Molekulargewicht | 601 aa, 68 kDa |
| Beobachtetes Molekulargewicht | 65-70 kDa |
| GenBank-Zugangsnummer | BC146562 |
| Gene symbol | ESCO2 |
| Gene ID (NCBI) | 157570 |
| Konjugation | Unkonjugiert |
| Form | Liquid |
| Reinigungsmethode | Antigen-affinitätsgereinigt |
| Lagerungspuffer | PBS only |
| Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
ESCO2 is also known as Establishment of Sister Chromatid Cohesion N-Acetyltransferase 2, EFO2. This gene encodes a member of the family of acetyltransferases involved in the establishment of sister chromatid cohesion during S phase and postreplicative sister chromatid cohesion induced by double-strand breaks (PubMed: 15821733). Mutations in the ESCO2 gene are associated with a rare genetic disorder called Roberts syndrome or SC phocomelia syndrome (PubMed: 16380922). The loss of function or impaired activity of the ESCO2 protein due to mutations disrupts the proper cohesion of sister chromatids, leading to chromosomal abnormalities and the characteristic features of Roberts syndrome. ESCO2 can be detected as about 65-70 kDa.





