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binds apoB, apoE, and triglyceride-rich lipoprotein (chylomicrons and very low density lipoprotein (VLDL)); may mediate the partitioning of dietary lipid between different tissues. De plus, nous expédions et et beaucoup plus de produits pour cette protéine.
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Human Polyclonal LSR Primary Antibody pour ICC, IF - ABIN4331132
Reaves, Fagan-Solis, Dunphy, Oliver, Scott, Fleming: The role of lipolysis stimulated lipoprotein receptor in breast cancer and directing breast cancer cell behavior. dans PLoS ONE 2014
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Human Polyclonal LSR Primary Antibody pour ICC, IHC - ABIN1176166
Hiramatsu, Serada, Enomoto, Takahashi, Nakagawa, Nojima, Morimoto, Matsuzaki, Yokoyama, Takahashi, Fujimoto, Takemori, Ueda, Yoshino, Morii, Kimura, Naka: LSR Antibody Therapy Inhibits Ovarian Epithelial Tumor Growth by Inhibiting Lipid Uptake. dans Cancer research 2017
this study shows that loss of tricellular tight junction protein LSR promotes cell invasion and migration via upregulation of TEAD1/AREG in endometrial cancer
Lipolysis-stimulated lipoprotein receptor (LSR)-deficient CaCo-2 cells exhibited increased cell proliferation.
Results of this study provide novel evidence that tricellular tight junctions protein LSR negatively regulates cancer cell progression and development in endometrial cancer.
Lipolysis-stimulated lipoprotein receptors (LSRs) localized to bicellular junctions in association with myosin regulatory light chain 2 (MRLC2) at low cell densities and to tricellular contacts when myosin phosphatase target subunit 1 (MYPT1) localized to the bicellular regions.
analysis of how Clostridium difficile binary toxin CDT interacts with its host cell receptor, Lipolysis-stimulated Lipoprotein Receptor
These data show that Clostridium difficile binary toxin CDT induces clustering of the lipolysis-stimulated lipoprotein receptor into lipid rafts.
findings show that Clostridium spiroforme toxin (CST)enters target cells via the lipolysis-stimulated lipoprotein receptor; findings indicate that CST shares LSR with C. difficile CDT and C. perfringens iota toxin as a host cell surface receptor
LSR defines tricellular contacts in epithelial cellular sheets by acting as a landmark to recruit tricellulin for tricellular tight junction formation.
LISCH7 may have a role in progression of human colon cancer
Data (including data from studies using transgenic mice) suggest that plasma and liver cholesterol homeostasis and hepatic expression of LDL receptor and lipolysis-stimulated lipoprotein receptor are modulated differently and independently by APOE allele (E4 versus E3) and docosahexaenoic acid intake. (APOE = apolipoprotein E)
Findings suggest that both tricellular tight junctions proteins TRIC and LSR have crucial roles for the differentiated cochlear cell survival.
The results of this study suggest that changes in cortex cholesterol regulation as a result of the LSR+/- genotype were linked to increased susceptibility to amyloid stress.
LSR is specifically expressed at tricellular junctions and that its expression correlates with the onset of blood-brain barrier formation during embryogenesis.
The activity of JNK1 and JNK2, but not JNK3, was required for the exclusive localization of angulin-1/LSR at the tTJs.
localization of angulin-1/LSR and tricellulin at tricellular contacts of brain and retinal endothelial cells in vivo
The results of this study suggested that a potential role of LSR in brain cholesterol distribution, which is particularly important in preserving neuronal integrity and thereby cognitive functions during aging.
expression of LSR is critical for liver and embryonic development [LSR]
LSR cooperates with the LDL receptor in the final hepatic processing of apoB-containing lipoproteins
binds apoB, apoE, and triglyceride-rich lipoprotein (chylomicrons and very low density lipoprotein (VLDL)); may mediate the partitioning of dietary lipid between different tissues
lipolysis stimulated lipoprotein receptor
, LISCH protein
, lipolysis-stimulated lipoprotein receptor-like
, immunoglobulin-like domain containing receptor 3
, lipolysis-stimulated lipoprotein receptor
, lipolysis-stimulated remnant
, liver-specific bHLH-Zip transcription factor
, lipolysis stimulated receptor
, lipolysis-stimulated receptor
, liver-specific gene on mouse chromosome 7 protein
, lipolysis-stimulated remnant receptor
, liver-specific bHLH-Zip transcription factor 7