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60S ribosomal protein L5 protein (GST)
| Name | 60S ribosomal protein L5 |
| Protein Type | Recombinant |
| Origin (Gene) |
Human |
| Conjugate |
GST
|
| Application |
SDS-PAGE (SDS), ELISA, Western Blotting (WB)
|
| Certificates | ISO 9001:2008 |
| Catalog no. | ABIN618787 |
| Quantity | 1 mg |
| Price | 3,199.00 $ Plus shipping costs $35.00 |
| Shipping to |
|
| Availability | Ships within 5 to 7 Business Days |
Additional Information
| Gene ID | NM_000969 |
| Sequence | GFVKVVKNKAYFKRYQVKFRRRREGKTDYYARKRLVIQDK NKYNTPKYRMIVRVTNRDIICQIAYARIEGDMIVCAAYAH ELPKYGVKVGLTNYAAAYCTGLLLARRLLNRFGMDKIYEG QVEVTGDEYNVESIDGQPGAFTCYLDAGLARTTTGNKVFG ALKGAVDGGLSIPHSTKRFPGYDSESKEFNAEVHRKHIMG QNVADYMRYLMEEDEDAYKKQFSQYIKNSVTPDMMEEMYK KAHAAIRENPVYEKKPKKEVKKKRWNRPKMSLAQKKDRVA QKKASFLRAQERAAES |
| Description | 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. |
| Molecular Weight | 34 KD |
