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rabbit anti mouse jagged1  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology rabbit anti mouse jagged1
    Serelaxin promotes the preservation of endothelial cell properties in both in vivo and in vitro by regulating candidate genes. (A) Heat map and (B) scatter plot show the genes with altered mRNA expression level in only TGFβ1-treated (x-axis) or in both TGFβ1- and Serelaxin-treated (y-axis) HCAECs. STEAP1, NOTCH1, <t>JAGGED1,</t> RAC1, DSP, GSC, ERBB3, FZD7, GSK3B and TGFB2 were significantly regulated by Serelaxin treatment, which is shown by separation from dot lines (cut-off by 4 folds). (C-D) qPCR analysis showing the expression of candidate genes, which were identified from qPCR array in TGFβ1- and Serelaxin-treated MCECs. Cells without any treatment were used as control. (E) qPCR analysis of the panel of candidate genes in vivo in sham and AAC-operated mice treated with vehicle or Serelaxin. Serelaxin significantly rescued the effects of AAC on all genes except for Gsc and Steap1. Student t-test was used for single comparison and one-way ANOVA with Bonferroni post-hoc analysis was used for multiple group comparisons. Gene expression and associated error bars, representing mean ± SEM n≥3, n.s. no significance, * p<0.05, ** p<0.01, *** p<0.001.
    Rabbit Anti Mouse Jagged1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 3859 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit anti mouse jagged1/product/Santa Cruz Biotechnology
    Average 96 stars, based on 3859 article reviews
    rabbit anti mouse jagged1 - by Bioz Stars, 2026-03
    96/100 stars

    Images

    1) Product Images from "Serelaxin alleviates cardiac fibrosis through inhibiting endothelial-to-mesenchymal transition via RXFP1"

    Article Title: Serelaxin alleviates cardiac fibrosis through inhibiting endothelial-to-mesenchymal transition via RXFP1

    Journal: Theranostics

    doi: 10.7150/thno.38640

    Serelaxin promotes the preservation of endothelial cell properties in both in vivo and in vitro by regulating candidate genes. (A) Heat map and (B) scatter plot show the genes with altered mRNA expression level in only TGFβ1-treated (x-axis) or in both TGFβ1- and Serelaxin-treated (y-axis) HCAECs. STEAP1, NOTCH1, JAGGED1, RAC1, DSP, GSC, ERBB3, FZD7, GSK3B and TGFB2 were significantly regulated by Serelaxin treatment, which is shown by separation from dot lines (cut-off by 4 folds). (C-D) qPCR analysis showing the expression of candidate genes, which were identified from qPCR array in TGFβ1- and Serelaxin-treated MCECs. Cells without any treatment were used as control. (E) qPCR analysis of the panel of candidate genes in vivo in sham and AAC-operated mice treated with vehicle or Serelaxin. Serelaxin significantly rescued the effects of AAC on all genes except for Gsc and Steap1. Student t-test was used for single comparison and one-way ANOVA with Bonferroni post-hoc analysis was used for multiple group comparisons. Gene expression and associated error bars, representing mean ± SEM n≥3, n.s. no significance, * p<0.05, ** p<0.01, *** p<0.001.
    Figure Legend Snippet: Serelaxin promotes the preservation of endothelial cell properties in both in vivo and in vitro by regulating candidate genes. (A) Heat map and (B) scatter plot show the genes with altered mRNA expression level in only TGFβ1-treated (x-axis) or in both TGFβ1- and Serelaxin-treated (y-axis) HCAECs. STEAP1, NOTCH1, JAGGED1, RAC1, DSP, GSC, ERBB3, FZD7, GSK3B and TGFB2 were significantly regulated by Serelaxin treatment, which is shown by separation from dot lines (cut-off by 4 folds). (C-D) qPCR analysis showing the expression of candidate genes, which were identified from qPCR array in TGFβ1- and Serelaxin-treated MCECs. Cells without any treatment were used as control. (E) qPCR analysis of the panel of candidate genes in vivo in sham and AAC-operated mice treated with vehicle or Serelaxin. Serelaxin significantly rescued the effects of AAC on all genes except for Gsc and Steap1. Student t-test was used for single comparison and one-way ANOVA with Bonferroni post-hoc analysis was used for multiple group comparisons. Gene expression and associated error bars, representing mean ± SEM n≥3, n.s. no significance, * p<0.05, ** p<0.01, *** p<0.001.

    Techniques Used: Preserving, In Vivo, In Vitro, Expressing, Control, Comparison, Gene Expression

    Serelaxin rescues the Notch1 pathway in AAC-operated hearts. Immunofluorescence staining of (A) Jagged1, (B) Notch1 and (C) NICD in combination with WGA and DAPI in sham and AAC-operated hearts treated with vehicle or Serelaxin. Quantifications showed that protein expressions of (D) Jagged1, (E) Notch1 and (F) NICD were downregulated in AAC-operated hearts and could be restored by Serelaxin. (G) Western blot analysis shows the amount of the soluble form of Jagged1 in the medium of TGFβ1-treated MCECs. Ponceau-S stained membrane picture indicates that an equal amount of total precipitated protein was loaded for both the control and TGFβ1-treated MCECs. Soluble Jagged1 was reduced in TGFβ1-treated MCECs as quantified by densitometry analysis (right panel). Student t-test was used for single comparison and one-way ANOVA with Bonferroni post-hoc analysis was used for multiple group comparisons. Gene expression and associated error bars, representing mean ± SEM, n≥3, n.s. no significance, * p<0.05, ** p<0.01, *** p<0.001.
    Figure Legend Snippet: Serelaxin rescues the Notch1 pathway in AAC-operated hearts. Immunofluorescence staining of (A) Jagged1, (B) Notch1 and (C) NICD in combination with WGA and DAPI in sham and AAC-operated hearts treated with vehicle or Serelaxin. Quantifications showed that protein expressions of (D) Jagged1, (E) Notch1 and (F) NICD were downregulated in AAC-operated hearts and could be restored by Serelaxin. (G) Western blot analysis shows the amount of the soluble form of Jagged1 in the medium of TGFβ1-treated MCECs. Ponceau-S stained membrane picture indicates that an equal amount of total precipitated protein was loaded for both the control and TGFβ1-treated MCECs. Soluble Jagged1 was reduced in TGFβ1-treated MCECs as quantified by densitometry analysis (right panel). Student t-test was used for single comparison and one-way ANOVA with Bonferroni post-hoc analysis was used for multiple group comparisons. Gene expression and associated error bars, representing mean ± SEM, n≥3, n.s. no significance, * p<0.05, ** p<0.01, *** p<0.001.

    Techniques Used: Immunofluorescence, Staining, Western Blot, Membrane, Control, Comparison, Gene Expression

    Antibodies used in Immunofluorescence staining
    Figure Legend Snippet: Antibodies used in Immunofluorescence staining

    Techniques Used: Immunofluorescence

    Primers used in qPCR assay for gene expression analysis
    Figure Legend Snippet: Primers used in qPCR assay for gene expression analysis

    Techniques Used: Gene Expression, Sequencing



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    Expression of <t>Jagged1</t> using immunohistochemical and immunofluorescence stains ( A ) in mice in control group ( a ), asthma group ( b ), gamma-secretase inhibitor (DAPT) + ovalbumin (OVA) group ( c ), Mycobacterium vaccae + OVA group ( d ), OVA + M. vaccae group ( e ), and its quantification ( B and C ). Data are reported as mean±SE relative percentage to the control group (n=8). ## P<0.01 vs control; **P <0.01 vs asthma group (ANVOA). Original magnification x400, scale bar=50 μm.
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    Santa Cruz Biotechnology rabbit anti mouse jagged1
    Serelaxin promotes the preservation of endothelial cell properties in both in vivo and in vitro by regulating candidate genes. (A) Heat map and (B) scatter plot show the genes with altered mRNA expression level in only TGFβ1-treated (x-axis) or in both TGFβ1- and Serelaxin-treated (y-axis) HCAECs. STEAP1, NOTCH1, <t>JAGGED1,</t> RAC1, DSP, GSC, ERBB3, FZD7, GSK3B and TGFB2 were significantly regulated by Serelaxin treatment, which is shown by separation from dot lines (cut-off by 4 folds). (C-D) qPCR analysis showing the expression of candidate genes, which were identified from qPCR array in TGFβ1- and Serelaxin-treated MCECs. Cells without any treatment were used as control. (E) qPCR analysis of the panel of candidate genes in vivo in sham and AAC-operated mice treated with vehicle or Serelaxin. Serelaxin significantly rescued the effects of AAC on all genes except for Gsc and Steap1. Student t-test was used for single comparison and one-way ANOVA with Bonferroni post-hoc analysis was used for multiple group comparisons. Gene expression and associated error bars, representing mean ± SEM n≥3, n.s. no significance, * p<0.05, ** p<0.01, *** p<0.001.
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    Image Search Results


    KEY RESOURCES TABLE

    Journal: Molecular cell

    Article Title: Systematic Characterization of Mutations Altering Protein Degradation in Human Cancers

    doi: 10.1016/j.molcel.2021.01.020

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Rabbit monoclonal anti-human/mouse JAG1 , Cell Signaling Technology , Cat#70109.

    Techniques: Control, Virus, Recombinant, In Vitro, Transfection, Western Blot, Capsules, Purification, Gel Extraction, cDNA Synthesis, RNA HS Assay, Plasmid Preparation, BIA-KA, Software, Adhesive

    Expression of Jagged1 using immunohistochemical and immunofluorescence stains ( A ) in mice in control group ( a ), asthma group ( b ), gamma-secretase inhibitor (DAPT) + ovalbumin (OVA) group ( c ), Mycobacterium vaccae + OVA group ( d ), OVA + M. vaccae group ( e ), and its quantification ( B and C ). Data are reported as mean±SE relative percentage to the control group (n=8). ## P<0.01 vs control; **P <0.01 vs asthma group (ANVOA). Original magnification x400, scale bar=50 μm.

    Journal: Brazilian Journal of Medical and Biological Research

    Article Title: Regulation of γδT17 cells by Mycobacterium vaccae through interference with Notch/Jagged1 signaling pathway

    doi: 10.1590/1414-431X20209551

    Figure Lengend Snippet: Expression of Jagged1 using immunohistochemical and immunofluorescence stains ( A ) in mice in control group ( a ), asthma group ( b ), gamma-secretase inhibitor (DAPT) + ovalbumin (OVA) group ( c ), Mycobacterium vaccae + OVA group ( d ), OVA + M. vaccae group ( e ), and its quantification ( B and C ). Data are reported as mean±SE relative percentage to the control group (n=8). ## P<0.01 vs control; **P <0.01 vs asthma group (ANVOA). Original magnification x400, scale bar=50 μm.

    Article Snippet: Then, the sections were washed twice with PBS and incubated with an avidin D solution for 10 min. Endogenous peroxidase was blocked using a biotin solution to inhibit endogenous biotin, washed again, and subsequently incubated with rabbit anti-mouse Jagged1 antibody (1:1000; D4Y1R, CST) overnight at 4°C.

    Techniques: Expressing, Immunohistochemical staining, Immunofluorescence, Control

    The mRNA expression of Jagged1 in lung tissues was determined using real-time PCR. Data are reported as mean±SE relative percentage to the control group (n=8). *P<0.05 vs control; # P<0.05 vs asthma group (ANOVA). OVA: ovalbumin; DAPT: gamma-secretase inhibitor.

    Journal: Brazilian Journal of Medical and Biological Research

    Article Title: Regulation of γδT17 cells by Mycobacterium vaccae through interference with Notch/Jagged1 signaling pathway

    doi: 10.1590/1414-431X20209551

    Figure Lengend Snippet: The mRNA expression of Jagged1 in lung tissues was determined using real-time PCR. Data are reported as mean±SE relative percentage to the control group (n=8). *P<0.05 vs control; # P<0.05 vs asthma group (ANOVA). OVA: ovalbumin; DAPT: gamma-secretase inhibitor.

    Article Snippet: Then, the sections were washed twice with PBS and incubated with an avidin D solution for 10 min. Endogenous peroxidase was blocked using a biotin solution to inhibit endogenous biotin, washed again, and subsequently incubated with rabbit anti-mouse Jagged1 antibody (1:1000; D4Y1R, CST) overnight at 4°C.

    Techniques: Expressing, Real-time Polymerase Chain Reaction, Control

    Correlation analysis between Jagged1 and γδT17 cells in lung tissues. A and B , The ratio of IL-17+γδT+ cells to T cells was measured in each group. C , The percentage of IL-17+γδT+ cells and the Jagged1 mRNA expression in lung tissues were positively correlated (r=0.46, P<0.05). Data are reported as mean±SE relative percentage to the control group (n=8). **P<0.01 vs control; *P<0.05, ## P<0.01 vs asthma group (ANOVA). OVA: ovalbumin; DAPT: gamma-secretase inhibitor.

    Journal: Brazilian Journal of Medical and Biological Research

    Article Title: Regulation of γδT17 cells by Mycobacterium vaccae through interference with Notch/Jagged1 signaling pathway

    doi: 10.1590/1414-431X20209551

    Figure Lengend Snippet: Correlation analysis between Jagged1 and γδT17 cells in lung tissues. A and B , The ratio of IL-17+γδT+ cells to T cells was measured in each group. C , The percentage of IL-17+γδT+ cells and the Jagged1 mRNA expression in lung tissues were positively correlated (r=0.46, P<0.05). Data are reported as mean±SE relative percentage to the control group (n=8). **P<0.01 vs control; *P<0.05, ## P<0.01 vs asthma group (ANOVA). OVA: ovalbumin; DAPT: gamma-secretase inhibitor.

    Article Snippet: Then, the sections were washed twice with PBS and incubated with an avidin D solution for 10 min. Endogenous peroxidase was blocked using a biotin solution to inhibit endogenous biotin, washed again, and subsequently incubated with rabbit anti-mouse Jagged1 antibody (1:1000; D4Y1R, CST) overnight at 4°C.

    Techniques: Expressing, Control

    Serelaxin promotes the preservation of endothelial cell properties in both in vivo and in vitro by regulating candidate genes. (A) Heat map and (B) scatter plot show the genes with altered mRNA expression level in only TGFβ1-treated (x-axis) or in both TGFβ1- and Serelaxin-treated (y-axis) HCAECs. STEAP1, NOTCH1, JAGGED1, RAC1, DSP, GSC, ERBB3, FZD7, GSK3B and TGFB2 were significantly regulated by Serelaxin treatment, which is shown by separation from dot lines (cut-off by 4 folds). (C-D) qPCR analysis showing the expression of candidate genes, which were identified from qPCR array in TGFβ1- and Serelaxin-treated MCECs. Cells without any treatment were used as control. (E) qPCR analysis of the panel of candidate genes in vivo in sham and AAC-operated mice treated with vehicle or Serelaxin. Serelaxin significantly rescued the effects of AAC on all genes except for Gsc and Steap1. Student t-test was used for single comparison and one-way ANOVA with Bonferroni post-hoc analysis was used for multiple group comparisons. Gene expression and associated error bars, representing mean ± SEM n≥3, n.s. no significance, * p<0.05, ** p<0.01, *** p<0.001.

    Journal: Theranostics

    Article Title: Serelaxin alleviates cardiac fibrosis through inhibiting endothelial-to-mesenchymal transition via RXFP1

    doi: 10.7150/thno.38640

    Figure Lengend Snippet: Serelaxin promotes the preservation of endothelial cell properties in both in vivo and in vitro by regulating candidate genes. (A) Heat map and (B) scatter plot show the genes with altered mRNA expression level in only TGFβ1-treated (x-axis) or in both TGFβ1- and Serelaxin-treated (y-axis) HCAECs. STEAP1, NOTCH1, JAGGED1, RAC1, DSP, GSC, ERBB3, FZD7, GSK3B and TGFB2 were significantly regulated by Serelaxin treatment, which is shown by separation from dot lines (cut-off by 4 folds). (C-D) qPCR analysis showing the expression of candidate genes, which were identified from qPCR array in TGFβ1- and Serelaxin-treated MCECs. Cells without any treatment were used as control. (E) qPCR analysis of the panel of candidate genes in vivo in sham and AAC-operated mice treated with vehicle or Serelaxin. Serelaxin significantly rescued the effects of AAC on all genes except for Gsc and Steap1. Student t-test was used for single comparison and one-way ANOVA with Bonferroni post-hoc analysis was used for multiple group comparisons. Gene expression and associated error bars, representing mean ± SEM n≥3, n.s. no significance, * p<0.05, ** p<0.01, *** p<0.001.

    Article Snippet: Rabbit Anti-Mouse Jagged1 , 1:50 , Santa Cruz , SC8303.

    Techniques: Preserving, In Vivo, In Vitro, Expressing, Control, Comparison, Gene Expression

    Serelaxin rescues the Notch1 pathway in AAC-operated hearts. Immunofluorescence staining of (A) Jagged1, (B) Notch1 and (C) NICD in combination with WGA and DAPI in sham and AAC-operated hearts treated with vehicle or Serelaxin. Quantifications showed that protein expressions of (D) Jagged1, (E) Notch1 and (F) NICD were downregulated in AAC-operated hearts and could be restored by Serelaxin. (G) Western blot analysis shows the amount of the soluble form of Jagged1 in the medium of TGFβ1-treated MCECs. Ponceau-S stained membrane picture indicates that an equal amount of total precipitated protein was loaded for both the control and TGFβ1-treated MCECs. Soluble Jagged1 was reduced in TGFβ1-treated MCECs as quantified by densitometry analysis (right panel). Student t-test was used for single comparison and one-way ANOVA with Bonferroni post-hoc analysis was used for multiple group comparisons. Gene expression and associated error bars, representing mean ± SEM, n≥3, n.s. no significance, * p<0.05, ** p<0.01, *** p<0.001.

    Journal: Theranostics

    Article Title: Serelaxin alleviates cardiac fibrosis through inhibiting endothelial-to-mesenchymal transition via RXFP1

    doi: 10.7150/thno.38640

    Figure Lengend Snippet: Serelaxin rescues the Notch1 pathway in AAC-operated hearts. Immunofluorescence staining of (A) Jagged1, (B) Notch1 and (C) NICD in combination with WGA and DAPI in sham and AAC-operated hearts treated with vehicle or Serelaxin. Quantifications showed that protein expressions of (D) Jagged1, (E) Notch1 and (F) NICD were downregulated in AAC-operated hearts and could be restored by Serelaxin. (G) Western blot analysis shows the amount of the soluble form of Jagged1 in the medium of TGFβ1-treated MCECs. Ponceau-S stained membrane picture indicates that an equal amount of total precipitated protein was loaded for both the control and TGFβ1-treated MCECs. Soluble Jagged1 was reduced in TGFβ1-treated MCECs as quantified by densitometry analysis (right panel). Student t-test was used for single comparison and one-way ANOVA with Bonferroni post-hoc analysis was used for multiple group comparisons. Gene expression and associated error bars, representing mean ± SEM, n≥3, n.s. no significance, * p<0.05, ** p<0.01, *** p<0.001.

    Article Snippet: Rabbit Anti-Mouse Jagged1 , 1:50 , Santa Cruz , SC8303.

    Techniques: Immunofluorescence, Staining, Western Blot, Membrane, Control, Comparison, Gene Expression

    Antibodies used in Immunofluorescence staining

    Journal: Theranostics

    Article Title: Serelaxin alleviates cardiac fibrosis through inhibiting endothelial-to-mesenchymal transition via RXFP1

    doi: 10.7150/thno.38640

    Figure Lengend Snippet: Antibodies used in Immunofluorescence staining

    Article Snippet: Rabbit Anti-Mouse Jagged1 , 1:50 , Santa Cruz , SC8303.

    Techniques: Immunofluorescence

    Primers used in qPCR assay for gene expression analysis

    Journal: Theranostics

    Article Title: Serelaxin alleviates cardiac fibrosis through inhibiting endothelial-to-mesenchymal transition via RXFP1

    doi: 10.7150/thno.38640

    Figure Lengend Snippet: Primers used in qPCR assay for gene expression analysis

    Article Snippet: Rabbit Anti-Mouse Jagged1 , 1:50 , Santa Cruz , SC8303.

    Techniques: Gene Expression, Sequencing

    Antibodies used in Immunofluorescence staining

    Journal: Theranostics

    Article Title: Serelaxin alleviates cardiac fibrosis through inhibiting endothelial-to-mesenchymal transition via RXFP1

    doi: 10.7150/thno.38640

    Figure Lengend Snippet: Antibodies used in Immunofluorescence staining

    Article Snippet: Rabbit Anti-Mouse Jagged1 , 1:50 , Santa Cruz , SC8303.

    Techniques: Immunofluorescence