pe cy7 anti mouse tcf1 Search Results


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Santa Cruz Biotechnology mouse anti human hnf1 α antibody
( A–F ) Renal expression of TGF-β1, IL-1β, HNF1α, PCSK9, LDLR, and SREBP2 proteins (immunohistochemical analysis software was used to analyze the optical density values in the images, and semi-quantitative values of positive expression in kidney tissues were obtained) and mRNAs (from RT-qPCR, relative to GAPDH) in the 4 groups at 4, 8, and 12 weeks. Values represent means ± standard errors of mean for groups of 8 mice each. For comparisons at the same time point: * P <0.05 versus CTL, # P <0.05 versus AWI. TGF-β1 – transforming growth factor beta 1; IL-1β – interleukin 1β; HNF1α – hepatocyte nuclear factor 1α; PCSK9 – pro-protein convertase subtilisin kexin type 9; LDLR – low-density lipoprotein receptor; SREBP2 – sterol regulatory element binding protein 2; RT-q-PCR – real-time quantitative polymerase chain reaction; GAPDH – glyceraldehyde 3-phosphate dehydrogenase; CLT – control group; AWI group – Adriamycin-induced nephrosis with inflammation group.
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Cell Signaling Technology Inc anti mouse tcf1 tcf7
( A–F ) Renal expression of TGF-β1, IL-1β, HNF1α, PCSK9, LDLR, and SREBP2 proteins (immunohistochemical analysis software was used to analyze the optical density values in the images, and semi-quantitative values of positive expression in kidney tissues were obtained) and mRNAs (from RT-qPCR, relative to GAPDH) in the 4 groups at 4, 8, and 12 weeks. Values represent means ± standard errors of mean for groups of 8 mice each. For comparisons at the same time point: * P <0.05 versus CTL, # P <0.05 versus AWI. TGF-β1 – transforming growth factor beta 1; IL-1β – interleukin 1β; HNF1α – hepatocyte nuclear factor 1α; PCSK9 – pro-protein convertase subtilisin kexin type 9; LDLR – low-density lipoprotein receptor; SREBP2 – sterol regulatory element binding protein 2; RT-q-PCR – real-time quantitative polymerase chain reaction; GAPDH – glyceraldehyde 3-phosphate dehydrogenase; CLT – control group; AWI group – Adriamycin-induced nephrosis with inflammation group.
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Cell Signaling Technology Inc hnf1a rabbit igg monoclonal
( A–F ) Renal expression of TGF-β1, IL-1β, HNF1α, PCSK9, LDLR, and SREBP2 proteins (immunohistochemical analysis software was used to analyze the optical density values in the images, and semi-quantitative values of positive expression in kidney tissues were obtained) and mRNAs (from RT-qPCR, relative to GAPDH) in the 4 groups at 4, 8, and 12 weeks. Values represent means ± standard errors of mean for groups of 8 mice each. For comparisons at the same time point: * P <0.05 versus CTL, # P <0.05 versus AWI. TGF-β1 – transforming growth factor beta 1; IL-1β – interleukin 1β; HNF1α – hepatocyte nuclear factor 1α; PCSK9 – pro-protein convertase subtilisin kexin type 9; LDLR – low-density lipoprotein receptor; SREBP2 – sterol regulatory element binding protein 2; RT-q-PCR – real-time quantitative polymerase chain reaction; GAPDH – glyceraldehyde 3-phosphate dehydrogenase; CLT – control group; AWI group – Adriamycin-induced nephrosis with inflammation group.
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Becton Dickinson pe anti-mouse tcf1 s33-966
CD8 + T cells activated in the presence of ex-IL-2 display stronger effector functions See also <xref ref-type=Figure S6 . 1.5 × 10 5 magnetically purified naive F5 CD8 + T cells labeled with CTV were activated with CpG-matured, NP68-loaded cDC at a ratio of cDC:CD8 = 1:10, in the presence or absence of ex-IL-2 (11,5 ng/mL). (A) Median Fluorescence Intensity (MFI) of TCF1 was measured on divided cells after 4 days of activation and the ratio between cells cultured in the absence and cells cultured in the presence of ex-IL-2 was calculated. (B and C) After 3, 4, or 5 days of activation, CD8 + T cells were restimulated for 2h with NP68 and the percentages of IFN-γ- (B) and GzmB- (C Left) expressing CD8 + T cells were measured on divided cells. Representative dot plots and individual percentages of GzmB + cells are also depicted (C Right). (D) Percentages of live EL4 target cells, loaded or not with NP68 peptide, after 4h of co-culture with effector CD8 + T cells activated for 5 days. Values from three independent experiments are presented. The results are expressed as the mean +SD. E:T ratio = effector:target ratio. The mean ± SD of six independent experiments is shown in panel A. The mean ± SEM of triplicate cultures from one representative experiment out of three independent experiments is shown in panel B and C (right). In A, the statistical significance of the difference between the mean value of ratios and the hypothetical value of 1 was determined by the one sample t-test. In D, the statistical significance of differences between F5 CD8 + cultured with or without ex-IL-2 at each E:T ratio was assessed by a two-way ANOVA followed by Sidak’s multiple comparison test (ns = p > 0.05, ∗∗ = p ≤ 0.01 and ∗∗∗ = p ≤ 0.001). " width="250" height="auto" />
Pe Anti Mouse Tcf1 S33 966, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cell Signaling Technology Inc anti-human/mouse tcf1/tcf7 af488 [c63d9]
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Anti Human/Mouse Tcf1/Tcf7 Af488 [C63d9], supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


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Journal: Cell

Article Title: DE NOVO EPIGENETIC PROGRAMS INHIBIT PD-1 BLOCKADE-MEDIATED T-CELL REJUVENATION

doi: 10.1016/j.cell.2017.06.007

Figure Lengend Snippet: Key Resources Table

Article Snippet: Anti-mouse/human Tcf1 (clone C63D9) , Cell Signaling , Cat#14456S.

Techniques: Virus, Recombinant, DNA Methylation Assay, Plasmid Preparation, Cloning, cDNA Synthesis, Microarray, Software, Methylation Sequencing, Flow Cytometry

( A–F ) Renal expression of TGF-β1, IL-1β, HNF1α, PCSK9, LDLR, and SREBP2 proteins (immunohistochemical analysis software was used to analyze the optical density values in the images, and semi-quantitative values of positive expression in kidney tissues were obtained) and mRNAs (from RT-qPCR, relative to GAPDH) in the 4 groups at 4, 8, and 12 weeks. Values represent means ± standard errors of mean for groups of 8 mice each. For comparisons at the same time point: * P <0.05 versus CTL, # P <0.05 versus AWI. TGF-β1 – transforming growth factor beta 1; IL-1β – interleukin 1β; HNF1α – hepatocyte nuclear factor 1α; PCSK9 – pro-protein convertase subtilisin kexin type 9; LDLR – low-density lipoprotein receptor; SREBP2 – sterol regulatory element binding protein 2; RT-q-PCR – real-time quantitative polymerase chain reaction; GAPDH – glyceraldehyde 3-phosphate dehydrogenase; CLT – control group; AWI group – Adriamycin-induced nephrosis with inflammation group.

Journal: Medical Science Monitor : International Medical Journal of Experimental and Clinical Research

Article Title: Inflammation Induces Lipid Deposition in Kidneys by Downregulating Renal PCSK9 in Mice with Adriamycin-Induced Nephropathy

doi: 10.12659/MSM.917312

Figure Lengend Snippet: ( A–F ) Renal expression of TGF-β1, IL-1β, HNF1α, PCSK9, LDLR, and SREBP2 proteins (immunohistochemical analysis software was used to analyze the optical density values in the images, and semi-quantitative values of positive expression in kidney tissues were obtained) and mRNAs (from RT-qPCR, relative to GAPDH) in the 4 groups at 4, 8, and 12 weeks. Values represent means ± standard errors of mean for groups of 8 mice each. For comparisons at the same time point: * P <0.05 versus CTL, # P <0.05 versus AWI. TGF-β1 – transforming growth factor beta 1; IL-1β – interleukin 1β; HNF1α – hepatocyte nuclear factor 1α; PCSK9 – pro-protein convertase subtilisin kexin type 9; LDLR – low-density lipoprotein receptor; SREBP2 – sterol regulatory element binding protein 2; RT-q-PCR – real-time quantitative polymerase chain reaction; GAPDH – glyceraldehyde 3-phosphate dehydrogenase; CLT – control group; AWI group – Adriamycin-induced nephrosis with inflammation group.

Article Snippet: Immunohistochemistry (IHC) was used to examine the expression of interleukin (IL)-1β, transforming growth factor beta 1 (TGF-β1), HNF1α, PCSK9, LDLR, and SREBP2 using the following antibodies: rabbit anti-rat IL-1β antibody (working dilution 1: 100; sc-7884, Santa Cruz Biotechnology, USA), rabbit anti-rat TGF-β1 (working dilution 1: 100; sc-146, Santa Cruz Biotechnology), mouse anti-human SREBP2 antibody (working dilution 1: 100; sc-271615, Santa Cruz Biotechnology), mouse anti-human HNF1 α antibody (working dilution 1: 100; sc-393668, Santa Cruz Biotechnology,), rabbit anti-rat LDLR antibody (working dilution 1: 100; ab30532, Abcam, UK), rabbit anti-rat PCSK9 antibody (working dilution 1: 100; ab31762, Abcam).

Techniques: Expressing, Immunohistochemical staining, Software, Quantitative RT-PCR, Binding Assay, Real-time Polymerase Chain Reaction, Control

Representative immunostaining results of renal tissues for HNF1α, PCSK9, LDLR, and SREBP2 in each group at 4, 8, and 12 weeks. Scale bars indicate 100 μm. HNF1α – hepatocyte nuclear factor 1α; PCSK9 – pro-protein convertase subtilisin kexin type 9; LDLR – low-density lipoprotein receptor; SREBP2 – sterol regulatory element binding protein 2.

Journal: Medical Science Monitor : International Medical Journal of Experimental and Clinical Research

Article Title: Inflammation Induces Lipid Deposition in Kidneys by Downregulating Renal PCSK9 in Mice with Adriamycin-Induced Nephropathy

doi: 10.12659/MSM.917312

Figure Lengend Snippet: Representative immunostaining results of renal tissues for HNF1α, PCSK9, LDLR, and SREBP2 in each group at 4, 8, and 12 weeks. Scale bars indicate 100 μm. HNF1α – hepatocyte nuclear factor 1α; PCSK9 – pro-protein convertase subtilisin kexin type 9; LDLR – low-density lipoprotein receptor; SREBP2 – sterol regulatory element binding protein 2.

Article Snippet: Immunohistochemistry (IHC) was used to examine the expression of interleukin (IL)-1β, transforming growth factor beta 1 (TGF-β1), HNF1α, PCSK9, LDLR, and SREBP2 using the following antibodies: rabbit anti-rat IL-1β antibody (working dilution 1: 100; sc-7884, Santa Cruz Biotechnology, USA), rabbit anti-rat TGF-β1 (working dilution 1: 100; sc-146, Santa Cruz Biotechnology), mouse anti-human SREBP2 antibody (working dilution 1: 100; sc-271615, Santa Cruz Biotechnology), mouse anti-human HNF1 α antibody (working dilution 1: 100; sc-393668, Santa Cruz Biotechnology,), rabbit anti-rat LDLR antibody (working dilution 1: 100; ab30532, Abcam, UK), rabbit anti-rat PCSK9 antibody (working dilution 1: 100; ab31762, Abcam).

Techniques: Immunostaining, Binding Assay

CD8 + T cells activated in the presence of ex-IL-2 display stronger effector functions See also <xref ref-type=Figure S6 . 1.5 × 10 5 magnetically purified naive F5 CD8 + T cells labeled with CTV were activated with CpG-matured, NP68-loaded cDC at a ratio of cDC:CD8 = 1:10, in the presence or absence of ex-IL-2 (11,5 ng/mL). (A) Median Fluorescence Intensity (MFI) of TCF1 was measured on divided cells after 4 days of activation and the ratio between cells cultured in the absence and cells cultured in the presence of ex-IL-2 was calculated. (B and C) After 3, 4, or 5 days of activation, CD8 + T cells were restimulated for 2h with NP68 and the percentages of IFN-γ- (B) and GzmB- (C Left) expressing CD8 + T cells were measured on divided cells. Representative dot plots and individual percentages of GzmB + cells are also depicted (C Right). (D) Percentages of live EL4 target cells, loaded or not with NP68 peptide, after 4h of co-culture with effector CD8 + T cells activated for 5 days. Values from three independent experiments are presented. The results are expressed as the mean +SD. E:T ratio = effector:target ratio. The mean ± SD of six independent experiments is shown in panel A. The mean ± SEM of triplicate cultures from one representative experiment out of three independent experiments is shown in panel B and C (right). In A, the statistical significance of the difference between the mean value of ratios and the hypothetical value of 1 was determined by the one sample t-test. In D, the statistical significance of differences between F5 CD8 + cultured with or without ex-IL-2 at each E:T ratio was assessed by a two-way ANOVA followed by Sidak’s multiple comparison test (ns = p > 0.05, ∗∗ = p ≤ 0.01 and ∗∗∗ = p ≤ 0.001). " width="100%" height="100%">

Journal: iScience

Article Title: Exogenous IL-2 delays memory precursors generation and is essential for enhancing memory cells effector functions

doi: 10.1016/j.isci.2024.109411

Figure Lengend Snippet: CD8 + T cells activated in the presence of ex-IL-2 display stronger effector functions See also Figure S6 . 1.5 × 10 5 magnetically purified naive F5 CD8 + T cells labeled with CTV were activated with CpG-matured, NP68-loaded cDC at a ratio of cDC:CD8 = 1:10, in the presence or absence of ex-IL-2 (11,5 ng/mL). (A) Median Fluorescence Intensity (MFI) of TCF1 was measured on divided cells after 4 days of activation and the ratio between cells cultured in the absence and cells cultured in the presence of ex-IL-2 was calculated. (B and C) After 3, 4, or 5 days of activation, CD8 + T cells were restimulated for 2h with NP68 and the percentages of IFN-γ- (B) and GzmB- (C Left) expressing CD8 + T cells were measured on divided cells. Representative dot plots and individual percentages of GzmB + cells are also depicted (C Right). (D) Percentages of live EL4 target cells, loaded or not with NP68 peptide, after 4h of co-culture with effector CD8 + T cells activated for 5 days. Values from three independent experiments are presented. The results are expressed as the mean +SD. E:T ratio = effector:target ratio. The mean ± SD of six independent experiments is shown in panel A. The mean ± SEM of triplicate cultures from one representative experiment out of three independent experiments is shown in panel B and C (right). In A, the statistical significance of the difference between the mean value of ratios and the hypothetical value of 1 was determined by the one sample t-test. In D, the statistical significance of differences between F5 CD8 + cultured with or without ex-IL-2 at each E:T ratio was assessed by a two-way ANOVA followed by Sidak’s multiple comparison test (ns = p > 0.05, ∗∗ = p ≤ 0.01 and ∗∗∗ = p ≤ 0.001).

Article Snippet: PE anti-mouse TCF1 (clone S33-966) , BD Biosciences , Cat#564217 (AB_2687845).

Techniques: Purification, Labeling, Fluorescence, Activation Assay, Cell Culture, Expressing, Co-Culture Assay, Comparison

Journal: iScience

Article Title: Exogenous IL-2 delays memory precursors generation and is essential for enhancing memory cells effector functions

doi: 10.1016/j.isci.2024.109411

Figure Lengend Snippet:

Article Snippet: PE anti-mouse TCF1 (clone S33-966) , BD Biosciences , Cat#564217 (AB_2687845).

Techniques: Virus, Modification, Western Blot, Recombinant, Cell Isolation, Staining, Enzyme-linked Immunosorbent Assay, Software

KEY RESOURCES TABLE

Journal: Immunity

Article Title: TCR-independent CD137 (4–1BB) signaling promotes CD8 + -exhausted T cell proliferation and terminal differentiation

doi: 10.1016/j.immuni.2023.06.007

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: Anti-human/mouse Tcf1/tcf7 AF488 [C63D9] , Cell Signaling Technology , Cat#: 6444S.

Techniques: Purification, Recombinant, Lysis, Negative Control, Cell Isolation, Staining, Knock-Out, Isolation, Control, Infection, RNA Sequencing, Software, Gene Expression