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anti rabbit igg bm2012  (Boster Bio)


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    Structured Review

    Boster Bio anti rabbit igg bm2012
    Anti Rabbit Igg Bm2012, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 40 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti rabbit igg bm2012/product/Boster Bio
    Average 93 stars, based on 40 article reviews
    anti rabbit igg bm2012 - by Bioz Stars, 2026-03
    93/100 stars

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    Molecular and cellular characterization of male and female gonadal somatic cells. A. Identification of the mRNA expression level of sex-related genes in male and female gonadal somatic cells by qRT-PCR. * P < 0.05, significant difference; ** P < 0.01, extremely significant difference. B. Detection of the expression changes of sex-related genes in male and female gonadal somatic cells by Western blot. C. Observation of the expression of FOXL2 and SOX9 in male and female gonadal somatic cells by immunofluorescence. Anti- FOXL2 / SOX9 <t>conjugated</t> to <t>FITC</t> was shown as a green fluorescence signal. Nucleus staining with DAPI was shown as a blue signal. Scale bars: 500 μm (upper), 100 μm (lower).
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    Molecular and cellular characterization of male and female gonadal somatic cells. A. Identification of the mRNA expression level of sex-related genes in male and female gonadal somatic cells by qRT-PCR. * P < 0.05, significant difference; ** P < 0.01, extremely significant difference. B. Detection of the expression changes of sex-related genes in male and female gonadal somatic cells by Western blot. C. Observation of the expression of FOXL2 and SOX9 in male and female gonadal somatic cells by immunofluorescence. Anti- FOXL2 / SOX9 conjugated to FITC was shown as a green fluorescence signal. Nucleus staining with DAPI was shown as a blue signal. Scale bars: 500 μm (upper), 100 μm (lower).

    Journal: Poultry Science

    Article Title: Construction and mechanism analysis of the sex reversal model of chicken gonadal somatic cells

    doi: 10.1016/j.psj.2025.105435

    Figure Lengend Snippet: Molecular and cellular characterization of male and female gonadal somatic cells. A. Identification of the mRNA expression level of sex-related genes in male and female gonadal somatic cells by qRT-PCR. * P < 0.05, significant difference; ** P < 0.01, extremely significant difference. B. Detection of the expression changes of sex-related genes in male and female gonadal somatic cells by Western blot. C. Observation of the expression of FOXL2 and SOX9 in male and female gonadal somatic cells by immunofluorescence. Anti- FOXL2 / SOX9 conjugated to FITC was shown as a green fluorescence signal. Nucleus staining with DAPI was shown as a blue signal. Scale bars: 500 μm (upper), 100 μm (lower).

    Article Snippet: For secondary staining, FITC Conjugated AffiniPure Mouse Anti-Rabbit IgG ( H + L ) (1:100, BM2012, Boster) was used for male cells, and FITC-conjugated AffiniPure Goat Anti-Mouse IgG ( H + L ) (1:100, BA1101, Boster) for female cells, respectively.

    Techniques: Expressing, Quantitative RT-PCR, Western Blot, Immunofluorescence, Fluorescence, Staining

    Flow cytometry analysis of the expression of FOXL2 and SOX9 in male and female gonadal somatic cells after treatment with FAD (50 nM) or E2 (50 nM, 100 nM). A. The expression level of FOXL2 and SOX9 in male and female gonadal somatic cells after treatment with FAD (50 nM) or E2 (50 nM, 100 nM) for 3d, 4d, or 13d. The horizontal axis represents the green fluorescence signal (FITC) of Anti- FOXL2 conjugated to FITC. The vertical axis represents the red fluorescence signal (PE) of Anti- SOX9 conjugated to ABflo® 594. N = 3. B. Statistical analysis of the expression of SOX9 in female gonadal cells treated with 50 nM FAD for 3 days. C. Statistical analysis of the expression of SOX9 in female gonadal cells treated with 50 nM FAD for 13 days. D. Statistical analysis of the expression of FOXL2 in female gonadal cells treated with 50 nM E2 for 3 days or 100 nM E2 for 4 days. E. Statistical analysis of the expression of FOXL2 in female gonadal cells treated with 50 nM FAD or 100 nM E2 for 13 days. B-E. Statistical analysis of protein expression relative to the corresponding Blank group. ** P < 0.01, *** P < 0.001, **** P < 0.0001; n = 3. All statistical comparisons were performed using Student’s t-test against the respective Blank group.

    Journal: Poultry Science

    Article Title: Construction and mechanism analysis of the sex reversal model of chicken gonadal somatic cells

    doi: 10.1016/j.psj.2025.105435

    Figure Lengend Snippet: Flow cytometry analysis of the expression of FOXL2 and SOX9 in male and female gonadal somatic cells after treatment with FAD (50 nM) or E2 (50 nM, 100 nM). A. The expression level of FOXL2 and SOX9 in male and female gonadal somatic cells after treatment with FAD (50 nM) or E2 (50 nM, 100 nM) for 3d, 4d, or 13d. The horizontal axis represents the green fluorescence signal (FITC) of Anti- FOXL2 conjugated to FITC. The vertical axis represents the red fluorescence signal (PE) of Anti- SOX9 conjugated to ABflo® 594. N = 3. B. Statistical analysis of the expression of SOX9 in female gonadal cells treated with 50 nM FAD for 3 days. C. Statistical analysis of the expression of SOX9 in female gonadal cells treated with 50 nM FAD for 13 days. D. Statistical analysis of the expression of FOXL2 in female gonadal cells treated with 50 nM E2 for 3 days or 100 nM E2 for 4 days. E. Statistical analysis of the expression of FOXL2 in female gonadal cells treated with 50 nM FAD or 100 nM E2 for 13 days. B-E. Statistical analysis of protein expression relative to the corresponding Blank group. ** P < 0.01, *** P < 0.001, **** P < 0.0001; n = 3. All statistical comparisons were performed using Student’s t-test against the respective Blank group.

    Article Snippet: For secondary staining, FITC Conjugated AffiniPure Mouse Anti-Rabbit IgG ( H + L ) (1:100, BM2012, Boster) was used for male cells, and FITC-conjugated AffiniPure Goat Anti-Mouse IgG ( H + L ) (1:100, BA1101, Boster) for female cells, respectively.

    Techniques: Flow Cytometry, Expressing, Fluorescence