- Featured Product
- KD/KO Validated
BCS1L Monoklonaler Antikörper
BCS1L Monoklonal Antikörper für WB, IHC, IF/ICC, Cytometric bead array, Indirect ELISA
Wirt / Isotyp
Maus / IgG1
Getestete Reaktivität
human, Maus
Anwendung
WB, IHC, IF/ICC, Cytometric bead array, Indirect ELISA
Konjugation
Unkonjugiert
CloneNo.
3G6H1
Kat-Nr. : 60212-1-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
60212-1-PBS bindet in WB, IHC, IF/ICC, Cytometric bead array, Indirect ELISA BCS1L und zeigt Reaktivität mit human, Maus
| Getestete Reaktivität | human, Maus |
| Wirt / Isotyp | Maus / IgG1 |
| Klonalität | Monoklonal |
| Typ | Antikörper |
| Immunogen | BCS1L fusion protein Ag18280 |
| Vollständiger Name | BCS1-like (yeast) |
| Berechnetes Molekulargewicht | 48 kDa |
| Beobachtetes Molekulargewicht | 47 kDa |
| GenBank-Zugangsnummer | BC007500 |
| Gene symbol | BCS1L |
| Gene ID (NCBI) | 617 |
| Konjugation | Unkonjugiert |
| Form | Liquid |
| Reinigungsmethode | Protein-G-Reinigung |
| Lagerungspuffer | PBS only |
| Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
Human BCS1-like (BCS1L), a mitochondrial inner-membrane protein, is a chaperone necessary for the assembly of mitochondrial respiratory chain complex III. Recently studies indicated that the mutations in this protein may cause the GRACILE (growth retardation, aminoaciduria, cholestasis, iron overload, lactacidosis, and early death) syndrome, a recessively inherited lethal disease characterized by fetal growth retardation, lactic acidosis, aminoaciduria, cholestasis, and abnormalities in iron metabolism.



















