Human SNX3 Recombinant Protein (RPPB4768)
- SKU:
- RPPB4768
- Product Type:
- Recombinant Protein
- Species:
- Human
- Uniprot:
- O60493
Description
| Product Name: | Human SNX3 Recombinant Protein |
| Product Code: | RPPB4768 |
| Size: | 20µg |
| Species: | Human |
| Target: | SNX3 |
| Synonyms: | Sorting nexin-3, Protein SDP3, SNX3, SDP3, Grd19, MCOPS8. |
| Source: | Escherichia Coli |
| Physical Appearance: | Sterile Filtered colorless solution. |
| Formulation: | SNX3 protein solution (1mg/ml) containing 20mM Tris-HCl buffer (pH 8.0), 1mM DTT, 20% glycerol and 0.1M NaCl. |
| Stability: | SNX3 Human Recombinant although stable at 4°C for 1 week, should be stored below -18°C. Please prevent freeze thaw cycles. |
| Purity: | Greater than 95.0% as determined by SDS-PAGE. |
| Amino Acid Sequence: | MGSSHHHHHH SSGLVPRGSH MAETVADTRR LITKPQNLND AYGPPSNFLE IDVSNPQTVG VGRGRFTTYE IRVKTNLPIF KLKESTVRRR YSDFEWLRSE LERESKVVVP PLPGKAFLRQ LPFRGDDGIF DDNFIEERKQ GLEQFINKVA GHPLAQNERC LHMFLQDEII DKSYTPSKIR HA |
Sorting nexin 3 (SNX3) belongs to the large family of hydrophilic proteins, which interact with various receptor types and are involved in intracellular trafficking. SNX3 interacts with phosphatidylinositol-3-phosphate, and is involved in protein trafficking. SNX3 comprises a distinct subgroup of nexins, which share less sequence similarity outside of the PX domain and have significantly different binding affinities for the tyrosine kinase receptors.
SNX3 produced in E.Coli is a single, non-glycosylated polypeptide chain containing 182 amino acids (1-162 a.a) and having a molecular mass of 20.9kDa.SNX3 is fused to a 20 amino acid His-tag at N-terminus & purified by proprietary chromatographic techniques.
| UniProt Protein Function: | SNX3: Phosphoinositide-binding protein required for multivesicular body formation. Specifically binds phosphatidylinositol 3-phosphate (PtdIns(P3)). Plays a role in protein transport between cellular compartments. Promotes stability and cell surface expression of epithelial sodium channel (ENAC) subunits SCNN1A and SCNN1G. Not involved in EGFR degradation. A chromosomal aberration involving SNX3 may be a cause of microphthalmia syndromic type 8 (MCOPS8). Translocation t(6;13)(q21;q12). Microphthalmia is a clinically heterogeneous disorder of eye formation, ranging from small size of a single eye to complete bilateral absence of ocular tissues (anophthalmia). In many cases, microphthalmia/anophthalmia occurs in association with syndromes that include non-ocular abnormalities. MCOPS8 is a very rare congenital syndrome characterized by microcephaly, microphthalmia, ectrodactyly of the lower limbs and prognathism. Intellectual deficit has been reported. Belongs to the sorting nexin family. 4 isoforms of the human protein are produced by alternative splicing. |
| UniProt Protein Details: | Protein type:Vesicle Chromosomal Location of Human Ortholog: 6q21 Cellular Component: clathrin-coated vesicle; cytoplasm; cytosol; early endosome; early endosome membrane; endosome membrane; extrinsic to membrane; retromer complex Molecular Function:phosphatidylinositol 3-phosphate binding; phosphatidylinositol-5-phosphate binding; protein binding; protein phosphatase binding Biological Process: membrane invagination; negative regulation of phagocytosis; negative regulation of protein catabolic process; negative regulation of protein transport; negative regulation of virion penetration into host cell; protein to membrane docking; regulation of Wnt receptor signaling pathway; response to bacterium; Wnt receptor signaling pathway Disease: Microphthalmia, Syndromic 8 |
| NCBI Summary: | This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like most family members. This protein interacts with phosphatidylinositol-3-phosphate, and is involved in protein trafficking. A pseudogene of this gene is present on the sex chromosomes. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014] |
| UniProt Code: | O60493 |
| NCBI GenInfo Identifier: | 12643620 |
| NCBI Gene ID: | 8724 |
| NCBI Accession: | O60493.3 |
| UniProt Secondary Accession: | O60493,O60718, Q4TT29, Q4TT31, Q5JXJ7, Q5JXJ8, Q96AP9 Q9C0J5, Q9NU45, A8K0B1, E1P5E4, E1P5E5, |
| UniProt Related Accession: | O60493 |
| Molecular Weight: | 16,316 Da |
| NCBI Full Name: | Sorting nexin-3 |
| NCBI Synonym Full Names: | sorting nexin 3 |
| NCBI Official Symbol: | SNX3�� |
| NCBI Official Synonym Symbols: | SDP3; Grd19; MCOPS8�� |
| NCBI Protein Information: | sorting nexin-3 |
| UniProt Protein Name: | Sorting nexin-3 |
| UniProt Synonym Protein Names: | Protein SDP3 |
| Protein Family: | Sorting nexin |
| UniProt Gene Name: | SNX3�� |
| UniProt Entry Name: | SNX3_HUMAN |
