Anti-SORT1 antibody (Cytoplasmic) (STJ13100340)

SKU:
STJ13100340-500

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Host: NZ White Rabbit
Applications: IHC/WB
Reactivity: Human
Note: STRICTLY FOR FURTHER SCIENTIFIC RESEARCH USE ONLY (RUO). MUST NOT TO BE USED IN DIAGNOSTIC OR THERAPEUTIC APPLICATIONS.
Short Description: Nz White Rabbit polyclonal antibody anti-Sortilin (Cytoplasmic) is suitable for use in Immunohistochemistry and Western Blot research applications.
Clonality: Polyclonal
Conjugation: Unconjugated
Isotype: IgG
Formulation: Shipped as lyophilised. Reconstitute in 500 µl of sterile water. Centrifuge to remove any insoluble material.
Purification: Ammonium sulphate precipitation
Dilution Range: A concentration of 10-50 µg/ml is recommended. The optimal concentration should be determined by the end user. Not yet tested in other applications.
Storage Instruction: Maintain the lyophilised/reconstituted antibodies frozen at-20°C for long term storage and refrigerated at 2-8°C for a shorter term. When reconstituting, glycerol (1:1) may be added for an additional stability. Avoid freeze and thaw cycles.
Gene Symbol: SORT1
Gene ID: 6272
Uniprot ID: SORT_HUMAN
Immunogen Region: Cytoplasmic
Specificity: Specific for Sortilin.
Immunogen: A synthetic peptide from the cytoplasmic domain of human Sortilin conjugated to blue carrier protein was used as the antigen.
Post Translational Modifications The N-terminal propeptide is cleaved by furin and possibly other homologous proteases. Palmitoylated. Undergoes cysteine S-palmitoylation which promotes the partitioning of the receptor into an endosomal membrane subdomain where it can interact with the retromer cargo-selective complex which mediates its retrograde trafficking to the Golgi apparatus. Phosphorylation at Ser-825 facilitates the interaction with GGA1.
Function Functions as a sorting receptor in the Golgi compartment and as a clearance receptor on the cell surface. Required for protein transport from the Golgi apparatus to the lysosomes by a pathway that is independent of the mannose-6-phosphate receptor (M6PR). Lysosomal proteins bind specifically to the receptor in the Golgi apparatus and the resulting receptor-ligand complex is transported to an acidic prelysosomal compartment where the low pH mediates the dissociation of the complex. The receptor is then recycled back to the Golgi for another round of trafficking through its binding to the retromer. Also required for protein transport from the Golgi apparatus to the endosomes. Promotes neuronal apoptosis by mediating endocytosis of the proapoptotic precursor forms of BDNF (proBDNF) and NGFB (proNGFB). Also acts as a receptor for neurotensin. May promote mineralization of the extracellular matrix during osteogenic differentiation by scavenging extracellular LPL. Probably required in adipocytes for the formation of specialized storage vesicles containing the glucose transporter SLC2A4/GLUT4 (GLUT4 storage vesicles, or GSVs). These vesicles provide a stable pool of SLC2A4 and confer increased responsiveness to insulin. May also mediate transport from the endoplasmic reticulum to the Golgi.
Protein Name Sortilin
100 Kda Nt Receptor
Glycoprotein 95
Gp95
Neurotensin Receptor 3
Nt3
Ntr3
Database Links Reactome: R-HSA-432722
Cellular Localisation Golgi Apparatus
Golgi Stack Membrane
Single-Pass Type I Membrane Protein
Endosome Membrane
Endoplasmic Reticulum Membrane
Nucleus Membrane
Cell Membrane
Extracellular Side
Lysosome Membrane
Localized To Membranes Of The Endoplasmic Reticulum
Endosomes
Golgi Stack
Lysosomes And Nucleus
A Small Fraction Of The Protein Is Also Localized To The Plasma Membrane
May Also Be Found In Slc2a4/Glut4 Storage Vesicles (Gsvs) In Adipocytes
Localization To The Plasma Membrane In Adipocytes May Be Enhanced By Insulin
Alternative Antibody Names Anti-Sortilin antibody
Anti-100 Kda Nt Receptor antibody
Anti-Glycoprotein 95 antibody
Anti-Gp95 antibody
Anti-Neurotensin Receptor 3 antibody
Anti-Nt3 antibody
Anti-Ntr3 antibody
Anti-SORT1 antibody

Information sourced from Uniprot.org

12 months for antibodies. 6 months for ELISA Kits. Please see website T&Cs for further guidance