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+49 (0)241 95 163 153 |
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+49 (0)241 95 163 155 |
60S ribosomal protein L5 protein (GST)
| Name | 60S ribosomal protein L5 |
| Protein-Typ | Recombinant |
| Herkunft (Gen) |
Human |
| Konjugat |
GST
|
| Applikation |
SDS-PAGE (SDS), ELISA, Western Blot (WB)
|
| Zertifikate | ISO 9001:2008 |
| Produktnummer | ABIN618787 |
| Menge | 1 mg |
| Preis | 2.494,78 € Zzgl. Versandkosten €20,00 und MWSt |
| Lieferung nach |
|
| Verfügbarkeit | Lieferung in 5 bis 7 Werktagen |
Produktbeschreibung
| Gen-ID | NM_000969 |
| Sequenz | GFVKVVKNKAYFKRYQVKFRRRREGKTDYYARKRLVIQDK NKYNTPKYRMIVRVTNRDIICQIAYARIEGDMIVCAAYAH ELPKYGVKVGLTNYAAAYCTGLLLARRLLNRFGMDKIYEG QVEVTGDEYNVESIDGQPGAFTCYLDAGLARTTTGNKVFG ALKGAVDGGLSIPHSTKRFPGYDSESKEFNAEVHRKHIMG QNVADYMRYLMEEDEDAYKKQFSQYIKNSVTPDMMEEMYK KAHAAIRENPVYEKKPKKEVKKKRWNRPKMSLAQKKDRVA QKKASFLRAQERAAES |
| Beschreibung | Background: Required for rRNA maturation and formation of the 60S ribosomal subunits. This protein binds 5S RNA. Defects in RPL5 are the cause of Diamond-Blackfan anemia type 6 (DBA6) [MIM:612561]. DBA6 is a form of Diamond-Blackfan anemia, a congenital non-regenerative hypoplastic anemia that usually presents early in infancy. Diamond-Blackfan anemia is characterized by a moderate to severe macrocytic anemia, erythroblastopenia, and an increased risk of malignancy. 30 to 40% of Diamond-Blackfan anemia patients present with short stature and congenital anomalies, the most frequent being craniofacial (Pierre-Robin syndrome and cleft palate), thumb and urogenital anomalies. |
| Molekulargewicht | 34 KD |



