Recombinant Human PITPnm 3 Protein
Beta LifeScience
SKU/CAT #: BLA-7047P
Recombinant Human PITPnm 3 Protein
Beta LifeScience
SKU/CAT #: BLA-7047P
Collections: Other recombinant proteins, Recombinant proteins
Our products are highly customizable to meet your specific needs. You can choose options such as endotoxin removal, liquid or lyophilized forms, preferred tags, and the desired functional sequence range for proteins. Submitting a written inquiry expedites the quoting process.
Product Overview
Host Species | Human |
Accession | Q9BZ71 |
Synonym | CORD5 Membrane associated phosphatidylinositol transfer protein 3 membrane-associated 3 Membrane-associated phosphatidylinositol transfer protein 3 MGC157740 MGC157741 NIR 1 NIR-1 NIR1 Phosphatidylinositol transfer protein Phosphatidylinositol transfer protein, membrane-associated 3 PITM3_HUMAN PITPNM PITPnm 3 PITPNM family member 3 Pitpnm3 PYK2 N terminal domain interacting receptor 1 Pyk2 N-terminal domain-interacting receptor 1 RDGBA3 Retinal degeneration B alpha 3 |
Description | Recombinant Human PITPnm 3 Protein was expressed in E.coli. It is a Protein fragment |
Source | E.coli |
Molecular Weight | 26 kDa |
Endotoxin | < 1.0 EU per μg of the protein as determined by the LAL method |
Formulation | Lyophilised |
Stability | The recombinant protein samples are stable for up to 12 months at -80°C |
Reconstitution | See related COA |
Unit Definition | For Research Use Only |
Storage Buffer | Shipped at 4°C. Store at -20°C. |
Target Details
Target Function | Catalyzes the transfer of phosphatidylinositol and phosphatidylcholine between membranes (in vitro). Binds calcium ions. |
Subcellular Location | Endomembrane system; Peripheral membrane protein. |
Protein Families | PtdIns transfer protein family, PI transfer class IIA subfamily |
Database References | |
Associated Diseases | Cone-rod dystrophy 5 (CORD5) |
Tissue Specificity | Detected in brain and spleen, and at low levels in ovary. |
Gene Functions References
- CCL18 can increase the invasive ability of non-small cell lung cancer cells by binding to its receptor Nir1. PMID: 26756176
- CCL18 enhances hepatocellular carcinoma (HCC) cell migration, invasion, and epithelial-mesenchymal transition (EMT) through the expression of PITPNM3 and the activation of the NF-kappaB signaling pathway. PMID: 26449829
- Data indicate that PYK2 N-terminal domain interacting receptor 1 (Nir1) could induce epithelial-mesenchymal transition by stabilising Snail via the PI3K/Akt/GSK3beta/Snail signalling pathway through binding to CCL18. PMID: 24001613
- Our observations of the PITPNM3 p.Q626H mutation carriers confirm that CORD5 is a disease not to mix with other retinal degenerations mapped to 17p13. PMID: 22405330
- CCL18 derived from Tumor-associated macrophages (TAMs) lays a critical role in promoting breast cancer metastasis via its receptor, PITPNM3. PMID: 21481794
- Thus, mutations in PITPNM3 do not appear to be a major cause of cone or cone-rod dystrophy. PMID: 20590364
- Our finding on the first mutation in the human homologue of Drosophila rdgB indicates novel pathways and a potential important role of the PITPNM3 in mammalian phototransduction. PMID: 17377520
- Mutation in the PYK2-binding domain of PITPNM3 causes autosomal dominant cone dystrophy (CORD5) in two Swedish families. PMID: 18188949