PHGDH Monoklonaler Antikörper
PHGDH Monoklonal Antikörper für WB, IHC, IF/ICC, IP, Indirect ELISA
Wirt / Isotyp
Maus / IgG1
Getestete Reaktivität
human, Maus, Ratte
Anwendung
WB, IHC, IF/ICC, IP, Indirect ELISA
Konjugation
Unkonjugiert
CloneNo.
1E8B8
Kat-Nr. : 67591-1-PBS
Synonyme
Geprüfte Anwendungen
Produktinformation
67591-1-PBS bindet in WB, IHC, IF/ICC, IP, Indirect ELISA PHGDH und zeigt Reaktivität mit human, Maus, Ratten
| Getestete Reaktivität | human, Maus, Ratte |
| Wirt / Isotyp | Maus / IgG1 |
| Klonalität | Monoklonal |
| Typ | Antikörper |
| Immunogen | PHGDH fusion protein Ag6877 |
| Vollständiger Name | phosphoglycerate dehydrogenase |
| Berechnetes Molekulargewicht | 57 kDa |
| Beobachtetes Molekulargewicht | 57 kDa |
| GenBank-Zugangsnummer | BC000303 |
| Gene symbol | PHGDH |
| Gene ID (NCBI) | 26227 |
| Konjugation | Unkonjugiert |
| Form | Liquid |
| Reinigungsmethode | Protein-G-Reinigung |
| Lagerungspuffer | PBS only |
| Lagerungsbedingungen | Store at -80°C. 20ul Größen enthalten 0,1% BSA. |
Hintergrundinformationen
PHGDH(D-3-phosphoglycerate dehydrogenase) is also named as 3-PGDH, PGDH3 and belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family. It catalyzes the transition of 3-phosphoglycerate into 3-phosphohydroxypyruvate, which is the first and rate-limiting step in the phosphorylated pathway of serine biosynthesis, using NAD+/NADH as a cofactor. 3-PGDH deficiency is a rare recessive inborn error in the biosynthesis of the amino acid L-serine characterized clinically by congenital microcephaly, psychomotor retardation, and intractable seizures(PMID:19235232 ).







