catalog number :
MBS135058
products full name :
Anti Human VLDL receptor, clone 1H10
products short name :
[VLDL receptor, clone 1H10]
other names :
[very low-density lipoprotein receptor isoform b; Very low-density lipoprotein receptor; very low-density lipoprotein receptor; VLDL-R; VLDL receptor; very low density lipoprotein receptor]
products gene name :
[VLDLR]
other gene names :
[VLDLR; VLDLR; CARMQ1; CHRMQ1; VLDLRCH; VLDL receptor; VLDL-R]
uniprot entry name :
VLDLR_HUMAN
host :
Hybridoma cell culture.
form :
Frozen liquid; 0.05M Sodium Phosphate; 0.1M NaCl; 1mM EDTA; pH 6.6
concentration :
4.74 mg/ml
storage stability :
Store at -70°C. Shelf Life: 5 years from delivery. Shipping: Ships in Dry Ice.
tested application :
ELISA (EIA), Western Blot (WB), BL
other info1 :
Immunogen: Recombinant fragment of soluble VLDL receptor containing ligand binding repeats 1-8 (sVLDLr1-8). Target: Recognises the C-terminus of VLDL receptor ligand binding domain (191-355). Target Molecular Weight: 85,000. Antigen: Recombinant fragment of soluble VLDL receptor containing ligand repeats 1-8 (sVLDLr1-8).
other info2 :
Extinction Coefficient: 1.36
products categories :
Receptor Associated Protein (RAP); Monoclonal Antibodies to Human VLDL Receptor
products description :
Monoclonal antibody produced in mouse. Useful for ELISA and western blot under non-reducing conditions. Binds to an epitope on the C-terminus of VLDL receptor ligand binding domain (amino acids 191-355, UniProtKB: locus VLDLR_HUMAN, accession P98155) and blocks apoE4 binding. Purified by immobilized Protein A. IgG1 class.
ncbi acc num :
NP_001018066.1
ncbi gb acc num :
NM_001018056.1
ncbi mol weight :
160,000
ncbi pathways :
Lissencephaly Gene (LIS1) In Neuronal Migration And Development Pathway (137984); Reelin Signaling Pathway (137980)
ncbi summary :
The low density lipoprotein receptor (LDLR) gene family consists of cell surface proteins involved in receptor-mediated endocytosis of specific ligands. This gene encodes a lipoprotein receptor that is a member of the LDLR family and plays important roles in VLDL-triglyceride metabolism and the reelin signaling pathway. Mutations in this gene cause VLDLR-associated cerebellar hypoplasia. Alternative splicing generates multiple transcript variants encoding distinct isoforms for this gene. [provided by RefSeq, Aug 2009]
uniprot summary :
VLDLR: Binds VLDL and transports it into cells by endocytosis. In order to be internalized, the receptor-ligand complexes must first cluster into clathrin-coated pits. Binding to Reelin induces tyrosine phosphorylation of Dab1 and modulation of Tau phosphorylation. Defects in VLDLR are the cause of cerebellar ataxia mental retardation and dysequilibrium syndrome type 1 (CMARQ1); also known as dysequilibrium syndrome (DES) or non- progressive cerebellar disorder with mental retardation. CMARQ1 is a congenital, non-progressive cerebellar ataxia associated with disturbed equilibrium, delayed ambulation, mental retardation and cerebellar hypoplasia. Additional features include short stature, strabismus, pes planus and, rarely, seizures. 2 isoforms of the human protein are produced by alternative splicing. Protein type: Membrane protein, integral; Receptor, misc. Chromosomal Location of Human Ortholog: 9p24. Cellular Component: membrane; plasma membrane; integral to membrane; coated pit; receptor complex. Molecular Function: low-density lipoprotein receptor activity; very-low-density lipoprotein receptor activity; very-low-density lipoprotein binding; protein binding; apolipoprotein binding; calcium ion binding; glycoprotein binding; calcium-dependent protein binding. Biological Process: cholesterol metabolic process; nervous system development; receptor-mediated endocytosis; positive regulation of protein kinase activity; ventral spinal cord development; negative regulation of transcription from RNA polymerase II promoter; lipid transport; signal transduction; memory. Disease: Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 1