Human RPS19 Recombinant Protein (RPPB4519)
- SKU:
- RPPB4519
- Product type:
- Recombinant Protein
- Size:
- 10ug
- Species:
- Human
- Target:
- RPS19
- Synonyms:
- Ribosomal protein S19
- DBA
- DBA1
- S19
- Source:
- Escherichia Coli
- Uniprot:
- P39019
Description
| Product Name: | Human RPS19 Recombinant Protein |
| Product Code: | RPPB4519 |
| Size: | 10µg |
| Species: | Human |
| Target: | RPS19 |
| Synonyms: | Ribosomal protein S19, DBA, DBA1, S19, 40S ribosomal protein S19, RPS19. |
| Source: | Escherichia Coli |
| Physical Appearance: | Sterile Filtered clear solution. |
| Formulation: | The RPS19 solution (0.25mg/ml) contains 20mM Tris-HCl buffer (pH 8.0) containing 0.2M NaCl, 40% glycerol and 2mM DTT. |
| Stability: | Store at 4°C if entire vial will be used within 2-4 weeks. Store frozen at -20°C for longer periods of time. For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).Avoid multiple freeze-thaw cycles. |
| Purity: | Greater than 85% as determined by SDS-PAGE. |
| Amino Acid Sequence: | MGSSHHHHHH SSGLVPRGSH MGSMPGVTVK DVNQQEFVRA LAAFLKKSGK LKVPEWVDTV KLAKHKELAP YDENWFYTRA ASTARHLYLR GGAGVGSMTK IYGGRQRNGV MPSHFSRGSK SVARRVLQAL EGLKMVEKDQ DGGRKLTPQG QRDLDRIAGQ VAAANKKH |
Ribosomal Protein S19, also known as RPS19, is a part of the S19E family of ribosomal proteins. RPS19 is located in the cytoplasm and required for pre-rRNA processing and maturation of 40S ribosomal subunits. Mutations in RPS19 trigger Diamond-Blackfan anemia, a constitutional erythroblastopenia characterized by absent or decreased erythroid precursors, in a subset of patients.
RPS19 Human Recombinant produced in E. coli is a single polypeptide chain containing 168 amino acids (1-145) and having a molecular mass of 18.4kDa. RPS19 is fused to a 23 amino acid His-tag at N-terminus & purified by proprietary chromatographic techniques.
| UniProt Protein Function: | RPS19: Required for pre-rRNA processing and maturation of 40S ribosomal subunits. Defects in RPS19 are the cause of Diamond-Blackfan anemia type 1 (DBA1). DBA1 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. Belongs to the ribosomal protein S19e family. |
| UniProt Protein Details: | Protein type:Translation; Ribosomal Chromosomal Location of Human Ortholog: 19q13.2 Cellular Component: cytoplasm; cytosol; focal adhesion; membrane; nucleolus; nucleoplasm; ribosome Molecular Function:fibroblast growth factor binding; protein binding; protein homodimerization activity; protein kinase binding; structural constituent of ribosome Biological Process: erythrocyte differentiation; maturation of SSU-rRNA; maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA); monocyte chemotaxis; mRNA catabolic process, nonsense-mediated decay; nucleolus organization and biogenesis; positive regulation of cell motility; protein tetramerization; response to extracellular stimulus; ribosomal small subunit assembly and maintenance; ribosomal small subunit biogenesis and assembly; rRNA processing; SRP-dependent cotranslational protein targeting to membrane; translation; translational initiation; viral transcription Disease: Diamond-blackfan Anemia 1 |
| NCBI Summary: | Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 40S subunit. The protein belongs to the S19E family of ribosomal proteins. It is located in the cytoplasm. Mutations in this gene cause Diamond-Blackfan anemia (DBA), a constitutional erythroblastopenia characterized by absent or decreased erythroid precursors, in a subset of patients. This suggests a possible extra-ribosomal function for this gene in erythropoietic differentiation and proliferation, in addition to its ribosomal function. Higher expression levels of this gene in some primary colon carcinomas compared to matched normal colon tissues has been observed. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008] |
| UniProt Code: | P39019 |
| NCBI GenInfo Identifier: | 730640 |
| NCBI Gene ID: | 6223 |
| NCBI Accession: | P39019.2 |
| UniProt Related Accession: | P39019 |
| Molecular Weight: | 16,060 Da |
| NCBI Full Name: | 40S ribosomal protein S19 |
| NCBI Synonym Full Names: | ribosomal protein S19 |
| NCBI Official Symbol: | RPS19 |
| NCBI Official Synonym Symbols: | DBA; S19; DBA1 |
| NCBI Protein Information: | 40S ribosomal protein S19 |
| UniProt Protein Name: | 40S ribosomal protein S19 |
| Protein Family: | Ribosomal protein |
| UniProt Gene Name: | RPS19 |
| UniProt Entry Name: | RS19_HUMAN |
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