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rabbit polyclonal anti sema3b antibody  (Novus Biologicals)


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    Structured Review

    Novus Biologicals rabbit polyclonal anti sema3b antibody
    Figure 1. Immunohistochemical localization of <t>SEMA3B</t> in different grades of endometrial cancer. C – control; G – grade of endometrial cancer. 200× magnification.
    Rabbit Polyclonal Anti Sema3b Antibody, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/rabbit polyclonal anti sema3b antibody/product/Novus Biologicals
    Average 90 stars, based on 1 article reviews
    rabbit polyclonal anti sema3b antibody - by Bioz Stars, 2026-05
    90/100 stars

    Images

    1) Product Images from "Expression of Semaphorin 3B (SEMA3B) in Various Grades of Endometrial Cancer"

    Article Title: Expression of Semaphorin 3B (SEMA3B) in Various Grades of Endometrial Cancer

    Journal: Medical Science Monitor

    doi: 10.12659/msm.916762

    Figure 1. Immunohistochemical localization of SEMA3B in different grades of endometrial cancer. C – control; G – grade of endometrial cancer. 200× magnification.
    Figure Legend Snippet: Figure 1. Immunohistochemical localization of SEMA3B in different grades of endometrial cancer. C – control; G – grade of endometrial cancer. 200× magnification.

    Techniques Used: Immunohistochemical staining, Control



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    Figure 1. Immunohistochemical localization of <t>SEMA3B</t> in different grades of endometrial cancer. C – control; G – grade of endometrial cancer. 200× magnification.
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    Thermo Fisher rabbit polyclonal anti-human sema3b
    Figure 1. Immunohistochemical localization of <t>SEMA3B</t> in different grades of endometrial cancer. C – control; G – grade of endometrial cancer. 200× magnification.
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    Santa Cruz Biotechnology rabbit polyclonal anti sema3b antibody
    <t>SEMA3B</t> is a target of miR-221. a Binding sites of miR-221 (the black letters ) on the SEMA3B mRNA 3′UTR. b An inverse correlation between miR-221 and SEMA3B was observed by Spearman correlation analysis in 30 cased of human glioma tissues. c Western blot was performed to detect the protein level of SEMA3B in NHA and U87MG cells with miR-221 overexpression or knockdown using miR-221 inhibitor or mimic (100 pM) for 48 h, respectively. d Luciferase reporter plasmids and miR-221 mimics were co-transfected to cells, and then the luciferase reporter assay was employed to detect luciferase activity. *p < 0.05; **p < 0.01.
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    Image Search Results


    Figure 1. Immunohistochemical localization of SEMA3B in different grades of endometrial cancer. C – control; G – grade of endometrial cancer. 200× magnification.

    Journal: Medical Science Monitor

    Article Title: Expression of Semaphorin 3B (SEMA3B) in Various Grades of Endometrial Cancer

    doi: 10.12659/msm.916762

    Figure Lengend Snippet: Figure 1. Immunohistochemical localization of SEMA3B in different grades of endometrial cancer. C – control; G – grade of endometrial cancer. 200× magnification.

    Article Snippet: The analysis of SEMA3B level changes was performed based on the immunohistochemical reaction with rabbit polyclonal anti-SEMA3B antibody (Novus Biological).

    Techniques: Immunohistochemical staining, Control

    SEMA3B is a target of miR-221. a Binding sites of miR-221 (the black letters ) on the SEMA3B mRNA 3′UTR. b An inverse correlation between miR-221 and SEMA3B was observed by Spearman correlation analysis in 30 cased of human glioma tissues. c Western blot was performed to detect the protein level of SEMA3B in NHA and U87MG cells with miR-221 overexpression or knockdown using miR-221 inhibitor or mimic (100 pM) for 48 h, respectively. d Luciferase reporter plasmids and miR-221 mimics were co-transfected to cells, and then the luciferase reporter assay was employed to detect luciferase activity. *p < 0.05; **p < 0.01.

    Journal: Biological Research

    Article Title: Suppression of miR-221 inhibits glioma cells proliferation and invasion via targeting SEMA3B

    doi: 10.1186/s40659-015-0030-y

    Figure Lengend Snippet: SEMA3B is a target of miR-221. a Binding sites of miR-221 (the black letters ) on the SEMA3B mRNA 3′UTR. b An inverse correlation between miR-221 and SEMA3B was observed by Spearman correlation analysis in 30 cased of human glioma tissues. c Western blot was performed to detect the protein level of SEMA3B in NHA and U87MG cells with miR-221 overexpression or knockdown using miR-221 inhibitor or mimic (100 pM) for 48 h, respectively. d Luciferase reporter plasmids and miR-221 mimics were co-transfected to cells, and then the luciferase reporter assay was employed to detect luciferase activity. *p < 0.05; **p < 0.01.

    Article Snippet: The rabbit polyclonal anti-SEMA3B antibody (code: sc-21204-R, 1:500 dilution) and the goat polyclonal anti-GAPDH antibody (code: sc-48167, 1:2,000 dilution) were both purchased from Santa Cruz Biotechnologies (CA, USA).

    Techniques: Binding Assay, Western Blot, Over Expression, Knockdown, Luciferase, Transfection, Reporter Assay, Activity Assay

    Knockdown endogenous SEMA3B reversed the effect of miR-221 Inhibitor. a Western blot showed SEMA3B level in a U87MG cells with SEMA3B gene stably silenced, b CCK-8 assay was employed to detect the cell proliferation in U87MG wild type and SEMA3B KD cells treated with scramble or miR-221 inhibitor (100 pM). Transwell assay without matrigel coated for testing cell migration ( c ) and transwell assay with matrigel coated was employed to detect the cell invasion ability ( d ) in U87MG cells treated with scramble or miR-221 inhibitor (100 pM). *p < 0.05; **p < 0.01.

    Journal: Biological Research

    Article Title: Suppression of miR-221 inhibits glioma cells proliferation and invasion via targeting SEMA3B

    doi: 10.1186/s40659-015-0030-y

    Figure Lengend Snippet: Knockdown endogenous SEMA3B reversed the effect of miR-221 Inhibitor. a Western blot showed SEMA3B level in a U87MG cells with SEMA3B gene stably silenced, b CCK-8 assay was employed to detect the cell proliferation in U87MG wild type and SEMA3B KD cells treated with scramble or miR-221 inhibitor (100 pM). Transwell assay without matrigel coated for testing cell migration ( c ) and transwell assay with matrigel coated was employed to detect the cell invasion ability ( d ) in U87MG cells treated with scramble or miR-221 inhibitor (100 pM). *p < 0.05; **p < 0.01.

    Article Snippet: The rabbit polyclonal anti-SEMA3B antibody (code: sc-21204-R, 1:500 dilution) and the goat polyclonal anti-GAPDH antibody (code: sc-48167, 1:2,000 dilution) were both purchased from Santa Cruz Biotechnologies (CA, USA).

    Techniques: Knockdown, Western Blot, Stable Transfection, CCK-8 Assay, Transwell Assay, Migration