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rabbit mab anti erg cell signaling technology cat  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit mab anti erg cell signaling technology cat
    Rabbit Mab Anti Erg Cell Signaling Technology Cat, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 174 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit mab anti erg cell signaling technology cat/product/Cell Signaling Technology Inc
    Average 96 stars, based on 174 article reviews
    rabbit mab anti erg cell signaling technology cat - by Bioz Stars, 2026-06
    96/100 stars

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    (A) Quantification of Pdgfb from total retina RNA was normalized to beta-actin , n=9-11 retinas from 9-11 mice per group. Average +/− SE is shown. *P < 0.05 by 1-way ANOVA with Tukey’s post hoc test. (B) Quantification of Pdgfb from total retina RNA was normalized to gapdh , n=5-7 retinas from 5-7 mice per group. Average +/− SE is shown. *P < 0.05 by 1-way ANOVA with Tukey’s post hoc test. ( C ) Images <t>of</t> <t>anti-LEF1</t> stain of parental bEnd.3 cells and a stable population of bEnd.3 cells overexpressing LEF1, generated by lentiviral transduction and selection with puromycin. Scale bar 100 µm. ( D ) Quantification of Pdgfb from total RNA of bEnd.3 cells after treatment with vehicle or F4L5.13. 2 technical replicates per biological replicate were averaged, n=3 biological replicates. Average +/− SE is shown. *P < 0.05 by unpaired Student’s t-test. ( E ) Quantification of Pdgfb from total RNA of stable bEnd.3-LEF1 cells after treatment with vehicle or F4L5.13. 2 technical replicates per biological replicate were averaged, n=3 biological replicates. Average +/− SE is shown. *P < 0.05 by unpaired Student’s t-test.
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    (A) Quantification of Pdgfb from total retina RNA was normalized to beta-actin , n=9-11 retinas from 9-11 mice per group. Average +/− SE is shown. *P < 0.05 by 1-way ANOVA with Tukey’s post hoc test. (B) Quantification of Pdgfb from total retina RNA was normalized to gapdh , n=5-7 retinas from 5-7 mice per group. Average +/− SE is shown. *P < 0.05 by 1-way ANOVA with Tukey’s post hoc test. ( C ) Images <t>of</t> <t>anti-LEF1</t> stain of parental bEnd.3 cells and a stable population of bEnd.3 cells overexpressing LEF1, generated by lentiviral transduction and selection with puromycin. Scale bar 100 µm. ( D ) Quantification of Pdgfb from total RNA of bEnd.3 cells after treatment with vehicle or F4L5.13. 2 technical replicates per biological replicate were averaged, n=3 biological replicates. Average +/− SE is shown. *P < 0.05 by unpaired Student’s t-test. ( E ) Quantification of Pdgfb from total RNA of stable bEnd.3-LEF1 cells after treatment with vehicle or F4L5.13. 2 technical replicates per biological replicate were averaged, n=3 biological replicates. Average +/− SE is shown. *P < 0.05 by unpaired Student’s t-test.
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    (A) Quantification of Pdgfb from total retina RNA was normalized to beta-actin , n=9-11 retinas from 9-11 mice per group. Average +/− SE is shown. *P < 0.05 by 1-way ANOVA with Tukey’s post hoc test. (B) Quantification of Pdgfb from total retina RNA was normalized to gapdh , n=5-7 retinas from 5-7 mice per group. Average +/− SE is shown. *P < 0.05 by 1-way ANOVA with Tukey’s post hoc test. ( C ) Images <t>of</t> <t>anti-LEF1</t> stain of parental bEnd.3 cells and a stable population of bEnd.3 cells overexpressing LEF1, generated by lentiviral transduction and selection with puromycin. Scale bar 100 µm. ( D ) Quantification of Pdgfb from total RNA of bEnd.3 cells after treatment with vehicle or F4L5.13. 2 technical replicates per biological replicate were averaged, n=3 biological replicates. Average +/− SE is shown. *P < 0.05 by unpaired Student’s t-test. ( E ) Quantification of Pdgfb from total RNA of stable bEnd.3-LEF1 cells after treatment with vehicle or F4L5.13. 2 technical replicates per biological replicate were averaged, n=3 biological replicates. Average +/− SE is shown. *P < 0.05 by unpaired Student’s t-test.
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    (A) Quantification of Pdgfb from total retina RNA was normalized to beta-actin , n=9-11 retinas from 9-11 mice per group. Average +/− SE is shown. *P < 0.05 by 1-way ANOVA with Tukey’s post hoc test. (B) Quantification of Pdgfb from total retina RNA was normalized to gapdh , n=5-7 retinas from 5-7 mice per group. Average +/− SE is shown. *P < 0.05 by 1-way ANOVA with Tukey’s post hoc test. ( C ) Images of anti-LEF1 stain of parental bEnd.3 cells and a stable population of bEnd.3 cells overexpressing LEF1, generated by lentiviral transduction and selection with puromycin. Scale bar 100 µm. ( D ) Quantification of Pdgfb from total RNA of bEnd.3 cells after treatment with vehicle or F4L5.13. 2 technical replicates per biological replicate were averaged, n=3 biological replicates. Average +/− SE is shown. *P < 0.05 by unpaired Student’s t-test. ( E ) Quantification of Pdgfb from total RNA of stable bEnd.3-LEF1 cells after treatment with vehicle or F4L5.13. 2 technical replicates per biological replicate were averaged, n=3 biological replicates. Average +/− SE is shown. *P < 0.05 by unpaired Student’s t-test.

    Journal: bioRxiv

    Article Title: A FZD4/LRP5 agonist restores pericyte coverage and vascular integrity by increasing PDGFB signaling

    doi: 10.64898/2026.03.13.711629

    Figure Lengend Snippet: (A) Quantification of Pdgfb from total retina RNA was normalized to beta-actin , n=9-11 retinas from 9-11 mice per group. Average +/− SE is shown. *P < 0.05 by 1-way ANOVA with Tukey’s post hoc test. (B) Quantification of Pdgfb from total retina RNA was normalized to gapdh , n=5-7 retinas from 5-7 mice per group. Average +/− SE is shown. *P < 0.05 by 1-way ANOVA with Tukey’s post hoc test. ( C ) Images of anti-LEF1 stain of parental bEnd.3 cells and a stable population of bEnd.3 cells overexpressing LEF1, generated by lentiviral transduction and selection with puromycin. Scale bar 100 µm. ( D ) Quantification of Pdgfb from total RNA of bEnd.3 cells after treatment with vehicle or F4L5.13. 2 technical replicates per biological replicate were averaged, n=3 biological replicates. Average +/− SE is shown. *P < 0.05 by unpaired Student’s t-test. ( E ) Quantification of Pdgfb from total RNA of stable bEnd.3-LEF1 cells after treatment with vehicle or F4L5.13. 2 technical replicates per biological replicate were averaged, n=3 biological replicates. Average +/− SE is shown. *P < 0.05 by unpaired Student’s t-test.

    Article Snippet: LEF1 was stained in PFA-fixed cells using rabbit anti-LEF1 (Cell Signaling, #2230S 1:100) and goat anti-rabbit Alexa Fluor-555 (Invitrogen, #A21428).

    Techniques: Staining, Generated, Transduction, Selection