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ATP1A2-Specific Polyklonaler Antikörper
ATP1A2-Specific Polyklonal Antikörper für WB, IHC, IP, Indirect ELISA
Wirt / Isotyp
Kaninchen / IgG
Getestete Reaktivität
human, Maus
Anwendung
WB, IHC, IP, Indirect ELISA
Konjugation
Unkonjugiert
Kat-Nr. : 55179-1-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
55179-1-PBS bindet in WB, IHC, IP, Indirect ELISA ATP1A2-Specific und zeigt Reaktivität mit human, Maus
| Getestete Reaktivität | human, Maus |
| Wirt / Isotyp | Kaninchen / IgG |
| Klonalität | Polyklonal |
| Typ | Antikörper |
| Immunogen | Peptid |
| Vollständiger Name | ATPase, Na+/K+ transporting, alpha 2 (+) polypeptide |
| Berechnetes Molekulargewicht | 112 kDa |
| Beobachtetes Molekulargewicht | 100 kDa |
| GenBank-Zugangsnummer | NM_000702 |
| Gene symbol | ATP1A2 |
| Gene ID (NCBI) | 477 |
| Konjugation | Unkonjugiert |
| Form | Liquid |
| Reinigungsmethode | Antigen-Affinitätsreinigung |
| Lagerungspuffer | PBS only |
| Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
ATP1A2, also named as KIAA0778, belongs to the cation transport ATPase (P-type) family and Type IIC subfamily. It is the catalytic component of the active enzyme, which catalyzes the hydrolysis of ATP coupled with the exchange of sodium and potassium ions across the plasma membrane. Defects in ATP1A2 are the cause of familial hemiplegic migraine type 2 (FHM2). Defects in ATP1A2 are a cause of alternating hemiplegia of childhood (AHC). This antibody is specific to ATP1A2.





















