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Thermo Fisher
snp lrp2 c 8822318 10 Snp Lrp2 C 8822318 10, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/apoe+lipoprotein/pmc07551427-163-37-30?v=Thermo+Fisher Average 88 stars, based on 1 article reviews
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Thermo Fisher
gene exp lrp10 hs00204094 m1 Gene Exp Lrp10 Hs00204094 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/apoe+lipoprotein/pmc03096560-93-37-6?v=Thermo+Fisher Average 92 stars, based on 1 article reviews
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ProSci Incorporated
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Millar Inc
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Thermo Fisher
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Bio-Rad
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Thermo Fisher
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Thermo Fisher
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Thermo Fisher
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Thermo Fisher
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Marburg GmbH
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TRICOR Systems
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Image Search Results
Journal: Frontiers in Physiology
Article Title: β-Cyclodextrins Decrease Cholesterol Release and ABC-Associated Transporter Expression in Smooth Muscle Cells and Aortic Endothelial Cells
doi: 10.3389/fphys.2016.00185
Figure Lengend Snippet: Cholesterol efflux from ABAE and SMCs . Cells were first labeled with [ 3 H]-cholesterol (0.5 μCi/mL) for 36 h at 37°C and then equilibrated for 24 h in DMEM/0.05% BSA at 37°C. Cellular [ 3 H]-cholesterol loads in DPM per μg of proteins were compared between ABAE and SMCs (A) . Data represent the mean ± SEM (in DPM/μg of proteins), with n = 6 from two sets of experiments. Paired- t -test was performed, *** p < 0.001 when compared with ABAE condition. [ 3 H]-cholesterol released from both cell types was then measured 6 h after medium supplementation with either BSA (control condition) or cholesterol acceptors [ApoA-I (20 μg/mL) or HDL (50 μg/mL)] at 37°C (B) . Data represent the mean ± SEM (in DPM/μg of proteins), with n = 6 from two sets of experiments. One-way ANOVA test followed by Bonferroni correction was performed in which *** p < 0.001 refers to the control condition and ### p < 0.001 refers to the matched HDL condition in ABAE.
Article Snippet: ApoA-I and
Techniques: Labeling, Control
Journal: Frontiers in Physiology
Article Title: β-Cyclodextrins Decrease Cholesterol Release and ABC-Associated Transporter Expression in Smooth Muscle Cells and Aortic Endothelial Cells
doi: 10.3389/fphys.2016.00185
Figure Lengend Snippet: Cholesterol release from ABAE (A,C) and from SMCs (B,D) upon CD-treatment . Cells were first labeled with [ 3 H]-cholesterol (0.5 μCi/mL) for 36 h at 37°C and then equilibrated in DMEM/0.05% BSA for 24 h at 37°C. [ 3 H]-cholesterol released in the medium from both cell types was then measured 6 h after medium supplementation with cholesterol acceptors [ApoA-I (20 μg/mL) or HDL (50 μg/mL)] at 37°C. The radioactivity contained in the culture medium, that corresponds to the cholesterol released from cells was measured. Data are expressed as the mean ± SEM (in DPM/μg of proteins, n = 6 from two sets of experiments). Statistical analysis: a one-way ANOVA followed by Dunnett's test for multiple comparisons in which * p < 0.05; *** p < 0.001 compared with the control condition (open bars) without any CD treatment.
Article Snippet: ApoA-I and
Techniques: Labeling, Radioactivity, Control
Journal: Frontiers in Physiology
Article Title: β-Cyclodextrins Decrease Cholesterol Release and ABC-Associated Transporter Expression in Smooth Muscle Cells and Aortic Endothelial Cells
doi: 10.3389/fphys.2016.00185
Figure Lengend Snippet: Effect of 10 μM T0901317 on cholesterol efflux to ApoA-I and HDL in ABAE (A) and SMCs (B) treated or nor with Rameβ . Cells were first labeled with [ 3 H]-cholesterol as previously described and incubated in the presence of 1 mM Rameβ, 10 μM T0901317 or both during 24 h. Then, [ 3 H]-cholesterol released in the medium from both cell types was measured 6 h after medium supplementation with either ApoA-I (20 μg/mL) or HDL (50 μg/mL). Data are expressed as the mean ± SEM (in DPM/μg of proteins, n = 6 from two sets of experiments). Control condition (without any treatment) is used as the reference level and set to 100%. Statistical analysis: a one-way ANOVA followed by Dunnett's test for multiple comparisons in which * p < 0.05; ** p < 0.01; *** p < 0.001 compared with the untreated condition (Control condition, open bars) and in which ## p < 0.01 when Rameβ + T0901317 condition was compared with Rameβ condition.
Article Snippet: ApoA-I and
Techniques: Labeling, Incubation, Control
Journal: PLoS ONE
Article Title: Genome wide profiling in oral squamous cell carcinoma identifies a four genetic marker signature of prognostic significance
doi: 10.1371/journal.pone.0174865
Figure Lengend Snippet: Concordance percentage for amplification of LRP12 (chr 8q), CCND1 (chr 11q), TPM2 (chr 9p), FSCN1 (chr 7p), EGFR (chr 7p), CLPTM1L (chr 5p) and deletion of CHL1 (chr 3p) and CSMD1 (chr 8p) identified using array CGH and validated using qPCR copy number analysis in OSCC samples.
Article Snippet: Copy number analysis was done on 66 OSCCs using TaqMan Copy Number Assay: LRP12 (
Techniques: Amplification
Journal: PLoS ONE
Article Title: Genome wide profiling in oral squamous cell carcinoma identifies a four genetic marker signature of prognostic significance
doi: 10.1371/journal.pone.0174865
Figure Lengend Snippet: Overall survival curves were analyzed according to ≥ 1 of genetic marker (EGFR, CCND1, TPM2 and LRP12) using Kaplan-Meier estimate with log-rank test.
Article Snippet: Copy number analysis was done on 66 OSCCs using TaqMan Copy Number Assay: LRP12 (
Techniques: Marker
Journal: PLoS ONE
Article Title: Genome wide profiling in oral squamous cell carcinoma identifies a four genetic marker signature of prognostic significance
doi: 10.1371/journal.pone.0174865
Figure Lengend Snippet: Multivariate cox regression model analysis of four combined genetic markers consisting of EGFR, TPM2, CCND1 and LRP12 in OSCC overall survival.
Article Snippet: Copy number analysis was done on 66 OSCCs using TaqMan Copy Number Assay: LRP12 (
Techniques: Marker
Journal: Translational Vision Science & Technology
Article Title: SZN-413, a FZD4 Agonist, as a Potential Novel Therapeutic for the Treatment of Diabetic Retinopathy
doi: 10.1167/tvst.11.9.19
Figure Lengend Snippet: FZD4 and LRP5, primary receptors for Wnt signaling in vascular endothelial cells. (A) FZD1–10 and LRP5 and LRP6 mRNA expression in HRMECs, bEnd.3 cells, and HUVECs quantified by quantitative polymerase chain reaction (qPCR) and normalized by the housekeeping gene Actin . Bars represent mean ± SD. (B) Data from Macosko et al. 31 were reanalyzed to derive scaled average gene expression by cell type of Wnt receptors in mouse retina. (C) Data from Menon et al. were reanalyzed to derive scaled average gene expression by cell type of Wnt receptors in human retina.
Article Snippet: RNA was quantified using TaqMan Fast Advanced Master Mix (
Techniques: Expressing, Real-time Polymerase Chain Reaction, Gene Expression