catalog number :
MBS426070
products type :
Blocking Peptide
products full name :
NIR1 / PITPNM3 Immunizing Peptide
products short name :
[NIR1 / PITPNM3]
products name syn :
[PITPNM3; NIR1; PITPNM family member 3; PYK2 N-terminal domain-interacting receptor 1; RDGBA3; CORD5; MGC157740; MGC157741; membrane-associated phosphatidylinositol transfer protein 3; retinal degeneration B alpha 3; NIR1 / PITPNM3]
other names :
[membrane-associated phosphatidylinositol transfer protein 3 isoform 1; Membrane-associated phosphatidylinositol transfer protein 3; membrane-associated phosphatidylinositol transfer protein 3; PITPNM family member 3; Phosphatidylinositol transfer protein, membrane-associated 3; PITPnm 3; Pyk2 N-terminal domain-interacting receptor 1; NIR-1]
products gene name :
[PITPNM3]
products gene name syn :
[NIR1]
other gene names :
[PITPNM3; PITPNM3; NIR1; ACKR6; CORD5; RDGBA3; PITPNM3; NIR1; PITPnm 3; NIR-1]
uniprot entry name :
PITM3_HUMAN
reactivity :
Hu,Rt,Ms,Bv,Cn.
sequence :
C-SWARGPPKFESVP
form :
100ug of dried peptide
storage stability :
Shipped at ambient temperature, store at -20 degree C
tested application :
ELISA, WB, IHC
ncbi acc num :
NP_112497.2
ncbi gb acc num :
NM_031220.3
ncbi summary :
This gene encodes a member of a family of membrane-associated phosphatidylinositol transfer domain-containing proteins. The calcium-binding protein has phosphatidylinositol (PI) transfer activity and interacts with the protein tyrosine kinase PTK2B (also known as PYK2). The protein is homologous to a Drosophila protein that is implicated in the visual transduction pathway in flies. Mutations in this gene result in autosomal dominant cone dystrophy. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Sep 2009]
uniprot summary :
PITPNM3: transfers phosphatidylinositol and phosphatidylcholine between membranes. Binds calcium ions. Interacts with Pyk2 via its C-terminus. Two splice-variant isoforms have been described. Protein type: Calcium-binding. Chromosomal Location of Human Ortholog: 17p13. Cellular Component: endomembrane system; integral to membrane; intracellular. Molecular Function: calcium ion binding; lipid binding; phosphatidylinositol transporter activity; protein binding; receptor tyrosine kinase binding. Biological Process: phosphatidylinositol metabolic process; phospholipid transport. Disease: Cone-rod Dystrophy 5