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VLDLR Antibody (Center) Blocking peptide

Synthetic peptide

     
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Product Information
Primary Accession P98155
Other Accession NP_003374.3
Clone Names 90625263
Additional Information
Gene ID 7436
Other Names Very low-density lipoprotein receptor, VLDL receptor, VLDL-R, VLDLR
Format Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
PrecautionsThis product is for research use only. Not for use in diagnostic or therapeutic procedures.
Protein Information
Name VLDLR
Function Multifunctional cell surface receptor that binds VLDL and transports it into cells by endocytosis and therefore plays an important role in energy metabolism. Binds also to a wide range of other molecules including Reelin/RELN or apolipoprotein E/APOE- containing ligands as well as clusterin/CLU (PubMed:24381170, PubMed:30873003). In the off-state of the pathway, forms homooligomers or heterooligomers with LRP8 (PubMed:30873003). Upon binding to ligands, homooligomers are rearranged to higher order receptor clusters that transmit the extracellular RELN signal to intracellular signaling processes by binding to DAB1 (PubMed:30873003). This interaction results in phosphorylation of DAB1 leading to the ultimate cell responses required for the correct positioning of newly generated neurons. Later, mediates a stop signal for migrating neurons, preventing them from entering the marginal zone (By similarity).
Cellular Location Cell membrane; Single-pass type I membrane protein Membrane, clathrin-coated pit; Single-pass type I membrane protein
Tissue Location Abundant in heart and skeletal muscle; also ovary and kidney; not in liver
Research Areas
Citations (0)
citation

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Background

The low density lipoprotein receptor (LDLR) gene familyconsists of cell surface proteins involved in receptor-mediatedendocytosis of specific ligands. This gene encodes a lipoproteinreceptor that is a member of the LDLR family and plays importantroles in VLDL-triglyceride metabolism and the reelin signalingpathway. Mutations in this gene cause VLDLR-associated cerebellarhypoplasia. Alternative splicing generates multiple transcriptvariants encoding distinct isoforms for this gene. [provided byRefSeq].

References

Sakai, K., et al. Brain Res. 1276, 11-21 (2009)Francis, P.J., et al. J. Med. Genet. 46(5):300-307(2009)Ananyeva, N.M., et al. Blood Coagul. Fibrinolysis 19(6):543-555(2008)Turkmen, S., et al. Eur. J. Hum. Genet. 16(9):1070-1074(2008)

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$ 277.78
Cat# BP5754c
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