Mouse VLDLR Antibody Summary
Thr25-Ala798
Accession # AAA59384
Applications
Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.
Scientific Data
VLDL R in Mouse Embryo. VLDL R was detected in immersion fixed frozen sections of mouse embryo using Mouse VLDL R Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2258) at 15 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Goat HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS008) and counter-stained with hematoxylin (blue). View our protocol for Chromogenic IHC Staining of Frozen Tissue Sections.
VLDL R in Mouse Kidney. VLDL R was detected in perfusion fixed frozen sections of mouse kidney using Goat Anti-Mouse VLDL R Antigen Affinity-purified Polyclonal Antibody (Catalog # AF2258) at 3 µg/mL for 1 hour at room temperature followed by incubation with the Anti-Goat IgG VisUCyte™ HRP Polymer Antibody (Catalog # VC004). Tissue was stained using DAB (brown) and counterstained with hematoxylin (blue). Specific staining was localized to cell membranes of convoluted tubules. View our protocol for IHC Staining with VisUCyte HRP Polymer Detection Reagents.
Reconstitution Calculator
Preparation and Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Background: VLDLR
VLDL R is a 105 kDa type I integral membrane protein that belongs to the LDL receptor family. It plays a significant role in lipid metabolism and in nervous system development and function (1, 2). Mouse VLDL R has a 770 amino acid (aa) extracellular domain (ECD) and a 54 aa cytoplasmic region. The ECD contains eight LDLR class A repeats, three EGF-like repeats, six LDLR class B repeats, and a juxtamembrane region that is rich in O-linked glycosylation (3, 4). The cytoplasmic domain contains one NPXY internalization motif. VLDL R is predominantly expressed in striated muscle, adipose tissue, brain, and endothelial cells lining capillaries and small arterioles (3-6). VLDL R participates in the tissue uptake of fatty acids from plasma by mediating the internalization of ApoE-containing lipoparticles (i.e. VLDL, beta ‑VLDL, and chylomicron remnants) (5, 7). VLDL R binds and internalizes lipoprotein lipase (LPL) and mediates its transport from the basolateral to the lumenal face of endothelial cells (6, 8). VLDL R knockout mice are characterized by reduced LPL activity, reduced serum triglyceride clearance, and a resistance to developing obesity (7, 9, 10). VLDL R influences breast cancer cell motility by mediating the uptake of uPAR-PAI1 complexes (6, 11). Lipoprotein accumulation via macrophage VLDL R is instrumental in promoting the formation of atherosclerotic plaques (12). In the nervous system, VLDL R and ApoE R2 interactions with Reelin are critical for neuronal migration and positioning in the developing brain (13). VLDL R also functions in adult hippocampal synapse maturation, synaptic plasticity, and memory formation (14, 15). The ECD of mouse VLDL R shares 95% aa sequence identity with human and rat VLDL R. Within shared regions, mouse VLDL R shares 55% and 53% aa sequence identity with ApoE R2 and LDL R, respectively.
- Qiu, S. et al. (2006) Neurobiol. Learn. Mem. 85:16.
- May, P. et al. (2005) Cell. Mol. Life Sci. 62:2325.
- Gafvels, M.E. et al. (1994) Endocrinology 135:387.
- Oka, K. et al. (1994) Eur. J. Biochem. 224:975.
- Wyne, K.L. et al. (1996) Arterioscler. Thromb. Vasc. Biol. 16:407.
- Argraves, K.M. et al. (1995) J. Biol. Chem. 270:26550.
- Goudriaan, J.R. et al. (2001) Arterioscler. Thromb. Vasc. Biol. 21:1488.
- Obunike, J.C. et al. (2001) J. Biol. Chem. 276:8934.
- Yagyu, H. et al. (2002) J. Biol. Chem. 277:10037.
- Goudriaan, J.R. et al. (2004) J. Lipid Res. 45:1475.
- Webb, D.J. et al. (1999) J. Biol. Chem. 274:7412.
- van Eck, M. et al. (2005) Atherosclerosis 183:230.
- Jossin, Y. et al. (2004) J. Neurosci. 24:514.
- Niu, S. et al. (2004) Neuron 41:71.
- Weeber, E.J. et al. (2002) J. Biol. Chem. 277:39944.
Product Datasheets
Citations for Mouse VLDLR Antibody
R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
19
Citations: Showing 1 - 10
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The Secreted Glycoprotein Reelin Suppresses the Proliferation and Regulates the Distribution of Oligodendrocyte Progenitor Cells in the Embryonic Neocortex
Authors: Himari Ogino, Tsuzumi Nakajima, Yuki Hirota, Kohki Toriuchi, Mineyoshi Aoyama, Kazunori Nakajima et al.
The Journal of Neuroscience
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SIRT3 deficiency exacerbates fatty liver by attenuating the HIF1 alpha -LIPIN 1 pathway and increasing CD36 through Nrf2.
Authors: Barroso, E, RodrIguez-RodrIguez, R Et al.
Cell Commun Signal
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VLDLR is not essential for reelin-induced neuronal aggregation but suppresses neuronal invasion into the marginal zone
Authors: Yuki Hirota, Kazunori Nakajima
Development
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Very low-density lipoprotein receptor increases in a liver-specific manner due to protein deficiency but does not affect fatty liver in mice
Authors: Y Oshio, Y Hattori, H Kamata, Y Ozaki-Masu, A Seki, Y Tsuruta, A Takenaka
Scientific Reports, 2021-04-13;11(1):8003.
Species: Mouse
Sample Types: Tissue Homogenates
Applications: Western Blot -
Reelin Can Modulate Migration of Olfactory Ensheathing Cells and Gonadotropin Releasing Hormone Neurons via the Canonical Pathway
Authors: L Dairaghi, E Flannery, P Giacobini, A Saglam, H Saadi, S Constantin, F Casoni, BW Howell, S Wray
Front Cell Neurosci, 2018-08-03;12(0):228.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC-Fr -
Mathematical model of early Reelin-induced Src family kinase-mediated signaling
Authors: H Hass, F Kipkeew, A Gauhar, E Bouché, P May, J Timmer, HH Bock
PLoS ONE, 2017-10-19;12(10):e0186927.
Species: Mouse
Sample Types: Cell Lysates
Applications: Western Blot -
Pericyte loss influences Alzheimer-like neurodegeneration in mice.
Authors: Sagare A, Bell R, Zhao Z, Ma Q, Winkler E, Ramanathan A, Zlokovic B
Nat Commun, 2013-01-01;4(0):2932.
Species: Mouse
Sample Types: Whole Cells
Applications: Blocking -
Smooth muscle-endothelial cell communication activates Reelin signaling and regulates lymphatic vessel formation.
J. Cell Biol., 2012-06-04;197(6):837-49.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
miR-200c regulates FGFR-dependent epithelial proliferation via Vldlr during submandibular gland branching morphogenesis.
Authors: Rebustini IT, Hayashi T, Reynolds AD
Development, 2011-11-24;139(1):191-202.
Species: Mouse
Sample Types: Whole Cells
Applications: ICC -
Exercise during pregnancy mitigates Alzheimer-like pathology in mouse offspring.
Authors: Herring A, Donath A, Yarmolenko M, Uslar E, Conzen C, Kanakis D, Bosma C, Worm K, Paulus W, Keyvani K
FASEB J., 2011-09-24;26(1):117-28.
Species: Mouse
Sample Types: Tissue Homogenates
Applications: Western Blot -
apoE isoform-specific disruption of amyloid beta peptide clearance from mouse brain.
Authors: Deane R, Sagare A, Hamm K, Parisi M, Lane S, Finn MB, Holtzman DM, Zlokovic BV
J. Clin. Invest., 2008-11-13;118(12):4002-13.
Species: Mouse
Sample Types: Whole Cells
Applications: Neutralization -
Bovine lactoferrin inhibits Japanese encephalitis virus by binding to heparan sulfate and receptor for low density lipoprotein.
Authors: Chien YJ, Chen WJ, Hsu WL, Chiou SS
Virology, 2008-07-21;379(1):143-51.
Species: Hamster
Sample Types: Whole Cells
Applications: Neutralization -
Expression of VLDLR in the retina and evolution of subretinal neovascularization in the knockout mouse model's retinal angiomatous proliferation.
Authors: Hu W, Jiang A, Liang J, Meng H, Chang B, Gao H, Qiao X
Invest. Ophthalmol. Vis. Sci., 2008-01-01;49(1):407-15.
Species: Mouse
Sample Types: Whole Tissue
Applications: IHC -
Disabled 1 Is Part of a Signaling Pathway Activated by Epidermal Growth Factor Receptor
Authors: Paula Dlugosz, Magdalena Teufl, Maximilian Schwab, Katharina Eva Kohl, Johannes Nimpf
International Journal of Molecular Sciences
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Differential Action of Reelin on Oligomerization of ApoER2 and VLDL Receptor in HEK293 Cells Assessed by Time-Resolved Anisotropy and Fluorescence Lifetime Imaging Microscopy.
Authors: Dlugosz Paula, Tresky Roland, Nimpf Johannes
Frontiers in Immunology
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Hepatic regulation of VLDL receptor by PPAR beta /δ and FGF21 modulates non-alcoholic fatty liver disease
Authors: Mohammad Zarei, Emma Barroso, Xavier Palomer, Jianli Dai, Patricia Rada, Tania Quesada-López et al.
Molecular Metabolism
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Xanthine oxidoreductase is involved in macrophage foam cell formation and atherosclerosis development.
Authors: Kushiyama A, Okubo H, Sakoda H, Kikuchi T, Fujishiro M, Sato H, Kushiyama S, Iwashita M, Nishimura F, Fukushima T, Nakatsu Y, Kamata H, Kawazu S, Higashi Y, Kurihara H, Asano T.
Arterioscler Thromb Vasc Biol;32(2):291-8.
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A low-carbohydrate ketogenic diet induces the expression of very-low-density lipoprotein receptor in liver and affects its associated metabolic abnormalities
Authors: Tetsuya Okuda
npj Science of Food
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Reelin-Nrp1 Interaction Regulates Neocortical Dendrite Development in a Context-Specific Manner
Authors: Takao Kohno, Keisuke Ishii, Yuki Hirota, Takao Honda, Makoto Makino, Takahiko Kawasaki et al.
The Journal of Neuroscience
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