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SLC6A8 Polyklonaler Antikörper
SLC6A8 Polyklonal Antikörper für WB, IHC, IF-P, Indirect ELISA
Wirt / Isotyp
Kaninchen / IgG
Getestete Reaktivität
human, Maus, Ratte
Anwendung
WB, IHC, IF-P, Indirect ELISA
Konjugation
Unkonjugiert
Kat-Nr. : 20299-1-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
20299-1-PBS bindet in WB, IHC, IF-P, Indirect ELISA SLC6A8 und zeigt Reaktivität mit human, Maus, Ratten
| Getestete Reaktivität | human, Maus, Ratte |
| Wirt / Isotyp | Kaninchen / IgG |
| Klonalität | Polyklonal |
| Typ | Antikörper |
| Immunogen | SLC6A8 fusion protein Ag14110 |
| Vollständiger Name | solute carrier family 6 (neurotransmitter transporter, creatine), member 8 |
| Berechnetes Molekulargewicht | 635 aa, 71 kDa |
| Beobachtetes Molekulargewicht | 65-70 kDa |
| GenBank-Zugangsnummer | BC012355 |
| Gene symbol | SLC6A8 |
| Gene ID (NCBI) | 6535 |
| Konjugation | Unkonjugiert |
| Form | Liquid |
| Reinigungsmethode | Antigen-Affinitätsreinigung |
| Lagerungspuffer | PBS only |
| Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
SLC6A8, also known as the sodium- and chloride-dependent creatine transporter 1 (CT1), plays a critical role in transporting creatine, a crucial molecule for energy metabolism, into cells. SLC6A8 belongs to the solute carrier family 6 (SLC6), responsible for transporting diverse molecules across cell membranes. SLC6A8 expression is highest in muscle, kidney, and other tissues with high energy demands. Mutations in SLC6A8 cause creatine transporter deficiency, an X-linked mental retardation disorder (PMID: 17465020).













