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anti-Mouse (Murine) Caveolin-1 Anticorps:
anti-Rat (Rattus) Caveolin-1 Anticorps:
anti-Human Caveolin-1 Anticorps:
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Human Monoclonal Caveolin-1 Primary Antibody pour FACS, ICC - ABIN152046
Souto, Vallega, Wharton, Vinten, Tranum-Jensen, Pilch: Immunopurification and characterization of rat adipocyte caveolae suggest their dissociation from insulin signaling. dans The Journal of biological chemistry 2003
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Human Polyclonal Caveolin-1 Primary Antibody pour WB - ABIN2801935
Glenney: The sequence of human caveolin reveals identity with VIP21, a component of transport vesicles. dans FEBS letters 1992
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Human Polyclonal Caveolin-1 Primary Antibody pour IHC - ABIN965753
Maggi, Biedi, Segat, Barbero, Panetta, Cordera: IGF-I induces caveolin 1 tyrosine phosphorylation and translocation in the lipid rafts. dans Biochemical and biophysical research communications 2002
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Rat (Rattus) Monoclonal Caveolin-1 Primary Antibody pour WB - ABIN2192105
Salani, Passalacqua, Maffioli, Briatore, Hamoudane, Contini, Cordera, Maggi: IGF-IR internalizes with Caveolin-1 and PTRF/Cavin in HaCat cells. dans PLoS ONE 2010
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Human Caveolin-1 Primary Antibody pour IHC - ABIN965752
Zhang, Wolf-Yadlin, Ross, Pappin, Rush, Lauffenburger, White: Time-resolved mass spectrometry of tyrosine phosphorylation sites in the epidermal growth factor receptor signaling network reveals dynamic modules. dans Molecular & cellular proteomics : MCP 2005
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Monoclonal Caveolin-1 Primary Antibody pour IF, IP - ABIN534131
Fork, Hitzel, Nichols, Tikkanen, Brandes: Flotillin-1 facilitates toll-like receptor 3 signaling in human endothelial cells. dans Basic research in cardiology 2014
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Human Polyclonal Caveolin-1 Primary Antibody pour ICC, IHC (fro) - ABIN3043803
Wang, Zhao, Wu, He, Qu, Zhao, Zhao, Li, Wang: Mechanistic analysis of taxol-induced multidrug resistance in an ovarian cancer cell line. dans Asian Pacific journal of cancer prevention : APJCP 2013
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Human Polyclonal Caveolin-1 Primary Antibody pour ICC, IHC (fro) - ABIN3044427
Shi, Li, Jia, Ji, Song, Cheng, Wu, Song, Zhang, Zhu, Yang: MicroRNA-199a-5p affects porcine preadipocyte proliferation and differentiation. dans International journal of molecular sciences 2015
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Dog (Canine) Polyclonal Caveolin-1 Primary Antibody pour FACS, ICC - ABIN152668
Li, Liu, Pilcher, Anderson: Cell-specific targeting of caveolin-1 to caveolae, secretory vesicles, cytoplasm or mitochondria. dans Journal of cell science 2001
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Human Polyclonal Caveolin-1 Primary Antibody pour ICC, IP - ABIN1742344
Ferru-Clément, Fresquet, Norez, Métayé, Becq, Kitzis, Thoreau: Involvement of the Cdc42 pathway in CFTR post-translational turnover and in its plasma membrane stability in airway epithelial cells. dans PLoS ONE 2015
These results point to intestinal epithelial cell CAV1 as a potential therapeutic target to lower circulating free fatty acids and LDL cholesterol.
Single epicardial cell transcriptome sequencing identifies Caveolin 1 as an essential factor in zebrafish heart regeneration.
The development of transgenic zebrafish lines expressing CLTA fused to dsRed and CAV1 fused to GFP is reported.
maternally expressed zebrafish Cav-1 regulates dorsoventral patterning by limiting nuclear translocation of active beta-catenin
These results support important and previously unanticipated roles for the Caveolin-1 isoforms in vertebrate organogenesis.
interactions of cav1 at lipid-exposed domains regulate the partition of the receptor into membrane raft microdomains
Cav1 is a neuroprotective factor in the acute ocular hypertension injury animal model. The protective effect of Cav1 was mediated by promoting the switch of the microglial phenotype from the neurotoxic pro-inflammatory M1 to the neuroprotective anti-inflammatory M2.
Mice exposed to treadmill exercise after cerebral ischemia showed a significant up-regulation in expression of caveolin-1 compared to non-exercised animals.
Cells respond to deletion of CAV1 by increasing synthesis of extracellular matrix.
oxLDL-mediated cellular senescence is associated with increased p47phox recruitment to caveolae and its binding to Cav1.
Caloric restriction improved the metabolic phenotype in CAV-1 Knock-out mice by increasing insulin sensitivity; nevertheless, this intervention also increased Cardiovascular risk by inappropriate adaptive responses in the Renin-angiotensin-aldosterone system and Blood pressure.
Study shows that callosal projection neuron subtype-specific expression of caveolin 1 identifies and characterizes a first molecular component that distinguishes this functionally unique projection neuron population, a population that expands in primates, and is prototypical of additional dual and higher-order projection neuron subtypes.
investigation points toward CAV1 as a dysregulated protein in follicle-derived B-cell malignancies without harboring a differential expression between more aggressive and indolent hematological malignancies.
We developed a protocol to label B16F10 cells with AuNPs-PEG-TAT that permits subsequent tracking of cells in mice. CAV1 overexpression was found to increase retention and transendothelial migration of B16F10 cells in the lung.
Cav-1 deletion is able to suppress High Fat Diet-induced oxidative stress and dyslipidemia in ApoE-/- mice.
Transplantation of a denuded aorta into carotid artery leads to plaque formation. Caveolin-1 knockout leads to increased plaque formation. Additional knockout of eNOS in Cav1-/- aortae reduces plaque formation.
the CAV1-/- mice were characterized by a low-grade systemic proinflammatory status, with a moderate increase in the IL-6, TNF-alpha, and IL-12p70 levels CAV1-/- circulating lymphocytes were more prone to cytokine production upon nonspecific stimulation than the wild-type lymphocytes
data suggest that lung cancer cells escape oncogene-induced premature senescence through down-regulation of caveolin-1 expression to progress from premalignant lesions to cancer.
This study defines ZNRF1 as a regulator of TLR4-induced inflammatory responses and reveals another mechanism for the regulation of TLR4 signalling through CAV1.
Renal Cav1 promotes water and salt reabsorption via modulation of NCC function and regulation of vascular eNOS.
Sirt1 preserves Cav1-dependent endothelial function by mitigating miR-204-mediated vascular endoplasmic reticulum stress.
Cav1 is an important inhibitor of TGF-β1/Smad signaling in hepatic stellate cell activation and collagen production.
the present study indicated that Cav-1-/- accelerated liver injury in a mouse model of liver fibrosis through enhancing oxidative stress, inflammatory response and fibrosis progression
MURC binds to Cav1 and inhibits the association of Cav1 with the active form of Galpha13, resulting in the facilitated association of the active form of Galpha13 with p115RhoGEF. These results reveal that MURC has a function in the development of pulmonary hypertension through modulating Rho/ROCK signaling.
The part of PKC regulation of CaV1.2 in the heart involves changes in channel's cellular fate. The mechanism of this PKC regulation appears to involve the C-terminus of alpha1C, possibly corroborating the previously proposed role of NT-CT interactions within alpha1C.
Findings suggest that CAV1 might be involved in apoptosis and proliferation regulation in pancreatic beta cells.
vimentin and nestin intermediate filaments interact with caveolae central component caveolin-1 (CAV-1) and importantly, restrain the intracellular trafficking of CAV-1 positive vesicles by serving as a physical barrier.
CAV-1 was segregated in high-density lipid droplets, consistent with the formation of membrane-enclosed lipid-rich vesicular structures
these data suggested that the elevated cav-1 promoted pituitary adenoma cells migration and invasion by regulating the interaction between EGR1 and KLF5.
Caveolin-1 is palmitoylated by ZDHHC7 and ZDHHC21.
the findings of this study suggest that the downregulation of Cav1 in fibroblasts is associated with an increased tumor proliferation rate in vivo and chemoresistance. Further studies are warranted to explore whether the targeting of Cav1 in the stroma may represent a novel therapeutic approach in pancreatic cancer.
Caveolin-1 plays a significant role in the pathogenesis of various carcinomas and its expression affects the survival of cancer patients.
Cav-1 stabilizes eNOS expression and regulates its activity, whereas eNOS-derived nitric oxide promotes caveola-mediated endocytosis.
Study results suggest a role for CAV1 down-regulation in linking the aberrant responsiveness to mechanical stimulation and extracellular matrix accumulation with the progression of keloids. The decrease of CAV1 contributed to the hyperactivation of fibrogenesis-associated RUNX2, a transcription factor germane to osteogenesis/chondrogenesis, and increased migratory ability in keloid fibroblasts.
No differences were observed for genotype and allele distributions in relation to rs4236601 in the CAV1/CAV2 region. The association of rs2157719 (CDKN2B-AS1) with the primary open angle glaucoma (POAG) phenotype corroborates previously published results, reinforcing the importance of this variant in POAG etiology.
Nitric oxide (NO) promotes the cancer stem cells -regulatory activity of Oct4 through a mechanism that involves complex formation between Oct4 and the scaffolding protein caveolin-1 (Cav-1). In the absence of NO, Oct4 forms a molecular complex with Cav-1, which promotes the ubiquitin-mediated proteasomal degradation of Oct4.
The expression of caveolin-1 was significantly higher in prostate cancer samples than in benign prostatic hyperplasia samples.
We conclude that the presence of CAV1 in EVs from metastatic breast cancer cells is associated with enhanced migration and invasiveness of recipient cells in vitro, suggesting that intercellular communication promoted by EVs containing CAV1 will likely favor metastasis in vivo.
rs1049334 polymorphismof CAV1 upgrade the risk of urinary cancer, while rs1049337 and rs7804372 polymorphisms may act as a protector of urinary cancer[systematic review]
Lack of Cav-1 expression inhibited autophagy activity in Thyroid follicular cells exposed to Th1 cytokines (IL-1beta and IFN-gamma), which might be a novel pathogenetic mechanism of Hashimoto's disease.
Data show that silencing of fatty acid synthase (FASN) and the downstream estrogen receptor alpha (ERalpha) resulted in suppression of cell growth via a caveolin-1 dependent mechanism.
Higher tumor Cav-1 levels and lower stromal Cav-1 levels were significantly associated with longer PFS of nab-paclitaxel and gemcitabine.
Data show that the caveolin-1 (CAV1) protein is involved in epidermal growth factor receptor 2 (HER2) cell membrane dynamics within the context of receptor endocytosis.
Caveolin-1 prevents palmitate-induced NF-kappaB signaling by inhibiting GPRC5B-phosphorylation.
using proteomics profiling, we identified a new protein, caveolin-1 that is significantly and consistently augmented in CLL cells after these lymphocytes interact with stromal cell lines.
Study shows that ITGB1-dependent upregulation of caveolin-1 (CAV1) switches TGFbeta signalling from tumour-suppressive to oncogenic in prostate cancer. work suggests TGFbeta signalling and beta1 integrins as potential therapeutic targets in prostate cancer over-expressing CAV1, and contributes to better understand the paradoxical dual role of TGFbeta in tumour biology.
Caveolin-1 is a modulator of fibroblast activation and a potential biomarker for gastric cancer
transcription factor Sp1 interacts with nucleotides -123/-114, indicating that Sp1 could play a key role in the transcriptional regulation of pig CAV-1
Two alternative transcript variants encode two isoforms, caveolin-1-alpha and -beta; Cav1 may be implicated in pathogenesis of Glasser's disease of swine.
The plasma membrane Na/K-ATPase-caveolin-1 interaction may represent an important sensing mechanism by which the cells regulate the sterol regulatory element-binding protein pathway.
The present study indicates that caveolin-containing rafts/caveolins such as caveolin-1 could play a modulating role during oligodendroglial differentiation and regeneration via NGF/TrkA signaling.
Cav-1 might be a candidate gene for carcass traits, and might provide valuable information for understanding the mechanism of caveolae signaling in fat deposition by using the animal model of pig
ATRA is able to ameliorate highfatinduced AS in rabbits, which is mediated through the activation of eNOS and downregulating CAV1 expression.
Caveolin-1 expression ameliorates nephrotic damage in a rabbit model of cholesterol-induced hypercholesterolemia.
8-Bromo-cAMP stimulated alpha-methyl-D-glucopyranoside uptake via Epac and PKA-dependent SGLTs expression and trafficking through cav-1 and F-actin in proximal tubule cells.
Caveolin-1 scaffolding domain residue phenylalanine 92 modulates Akt signaling
Data show that resveratrol (Res) reversed caveolin-1 (Cav-1)/endothelial nitric oxide synthase (eNOS) expressions in high glucose cultured bovine aortic endothelial cells (BAECs).
these data provide the first detailed analysis of Cav-1 binding to one of its most significant client proteins, eNOS.
Study identifies a critical role of caveolin-1 in the regulation of eNOS uncoupling via a biopterin-dependent mechanism.
Data indicate that caveolin-1 expression is required for insulin uptake by aortic endothelial cells.
caveolin-1 is not required for the targeting of signaling molecules to caveolae/lipid rafts
integrin activation with shear stress results in SFK-regulated caveolin-1 phosphorylation that, in turn, mediates Csk association at integrin sites, where it plays a role in downstream, shear-stimulated myelin light chain diphosphorylation.
importance of CAV1 amino acids 89-95 and particularly F92 in mediating eNOS inhibition by AP-Cav and Cav-1
When endothelial cells were exposed to shear stress, caveolin-1 was transiently dephosphorylated.
alphaCAV1 likely contributes to control the increase in membrane signaling that occurs at the time of ovulation and luteinization.
caveolin-1 tyrosine 14 phosphorylation has a role in cell adhesion and migration
caveolin-1 Tyr(14) is necessary for binding to intermediate filaments, which in turn is required for anterior polarization of caveolin-1 in transmigrating cells
Phosphorylation of CAV1 in bovine rod outer segments in vitro by an endogenous tyrosine kinase is reported.
XIAP plays a novel role in endothelial cells, interacting with caveolin-1 and acting as a regulator of vascular antiatherogenic function.
These data show that insulin acutely regulates eNOS and CAV-1 trafficking to plasma membrane of vascular endothelial cells where their interaction can regulate eNOS activity.
TGF-beta1 downregulates caveolin-1 of cultured endothelial cells, involving ALK-5 receptor subtype
results suggest that cell division control protein 42(CDC42) activation is favored by the disruption of the caveolin-1-CDC42 interaction, allowing for its participation in the regulation of capacitation and the acrosome reaction
These data link RABS-5 and VPS-45 ciliary functions to the processing of periciliary-derived endocytic vesicles and regulation of ciliary membrane homeostasis. Our findings also provide insight into the regulation of PKD-2 ciliary levels via integrated endosomal sorting and CAV-1-mediated endocytosis.
The distribution of CAV-1 is highly dynamic during development and provides new insights into the sorting mechanisms that regulate CAV-1 localization.
The scaffolding protein encoded by this gene is the main component of the caveolae plasma membranes found in most cell types. The protein links integrin subunits to the tyrosine kinase FYN, an initiating step in coupling integrins to the Ras-ERK pathway and promoting cell cycle progression. The gene is a tumor suppressor gene candidate and a negative regulator of the Ras-p42/44 mitogen-activated kinase cascade. Caveolin 1 and caveolin 2 are located next to each other on chromosome 7 and express colocalizing proteins that form a stable hetero-oligomeric complex. Mutations in this gene have been associated with Berardinelli-Seip congenital lipodystrophy. Alternatively spliced transcripts encode alpha and beta isoforms of caveolin 1.
, caveolin 1
, caveolin, caveolae protein 1
, caveolin, caveolae protein, 22 kDa
, caveolin caveolae protein 22 kDa
, vesicular integral-membrane protein VIP21
, cell growth-inhibiting protein 32
, testis derived transcript