VSX2 Monoklonaler Antikörper
VSX2 Monoklonal Antikörper für WB, Indirect ELISA
Wirt / Isotyp
Maus / IgG2b
Getestete Reaktivität
human, Maus, Ratte
Anwendung
WB, Indirect ELISA
Konjugation
Unkonjugiert
CloneNo.
2C7C1
Kat-Nr. : 67626-1-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
67626-1-PBS bindet in WB, Indirect ELISA VSX2 und zeigt Reaktivität mit human, Maus, Ratten
| Getestete Reaktivität | human, Maus, Ratte |
| Wirt / Isotyp | Maus / IgG2b |
| Klonalität | Monoklonal |
| Typ | Antikörper |
| Immunogen | VSX2 fusion protein Ag29867 |
| Vollständiger Name | visual system homeobox 2 |
| Berechnetes Molekulargewicht | 361 aa, 39 kDa |
| Beobachtetes Molekulargewicht | 45 kDa |
| GenBank-Zugangsnummer | BC128153 |
| Gene symbol | VSX2 |
| Gene ID (NCBI) | 338917 |
| Konjugation | Unkonjugiert |
| Form | Liquid |
| Reinigungsmethode | Protein-A-Reinigung |
| Lagerungspuffer | PBS only |
| Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
VSX2, also named as CHX10 and HOX10, belongs to the paired homeobox family. VSX2 plays a significant role in the specification and morphogenesis of the sensory retina. It may also participate in the development of the cells of the inner nuclear layer, particularly bipolar cells. Defects in VSX2 are the cause of microphthalmia isolated type 2 (MCOP2). Defects in VSX2 are the cause of microphthalmia with cataracts and iris abnormalities (MCOPCTI). Defects in VSX2 are the cause of microphthalmia isolated with coloboma type 3 (MCOPCB3). The antibody is specific to VSX2.



