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rabbit anti zo2  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc rabbit anti zo2
    Rabbit Anti Zo2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 94/100, based on 96 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+zo2/Phospho-CREB+(Ser133)+Rabbit+mAb/pm37643760-69-18-35
    Average 94 stars, based on 96 article reviews
    rabbit anti zo2 - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Western Blot:

    Article Title: Raptor directs Sertoli cell cytoskeletal organization and polarity in the mouse testis.
    Article Snippet: Antibody(RRID) Vendor Catalog number Application Working Dilution for WB or (IF/IHC) Rabbit anti-Wilms Tumor1 (AB_2043201) Abcam Cambridge, MA,USA Ab89901 IF (1:200) Rabbit anti-ACTA2 (AB 2721021) ABclonal Shanghai, PRC A7248 IF (1:200) Rabbit anti-Raptor (AB 185538) Bethyl Montgomery,Alabama,USA A300–506A WB,IF 1:3000 (1:200) Rabbit anti-Vimentin (AB 1663663) Bioworld Louis Park, MN,USA BS1491 IF (1:200) Rabbit anti-Rheb (AB 2721022) Cell Signaling Technology Shanghai, PRC 13 879 WB 1:1000 Rabbit anti-Ki67 (AB 2687446) Cell Signaling Technology Shanghai, PRC 9129 IF (1:100) Rabbit anti-β-catenin (AB 331149) Cell Signaling Technology Shanghai, PRC 9562 IF (1:200) Rabbit anti-ZO1 (AB 10898025) Cell Signaling Technology Shanghai, PRC 8193 IF (1:100) Rabbit anti-ZO2 (AB 2203575) Cell Signaling Technology Shanghai, PRC 2847 IF (1:100) Rabbit anti-p-mTOR (AB 330970) Cell Signaling Technology Shanghai, PRC 2971 WB 1:1000 Rabbit anti-mTOR (AB 2105622) Cell Signaling Technology Shanghai, PRC 2983 WB 1:1000 Rabbit anti-p-p70S6K (AB 330944) Cell Signaling Technology Shanghai, PRC 9205 WB 1:2000 Rabbit anti-p70S6K (AB 390722) Cell Signaling Technology Shanghai, PRC 2708 WB 1:1000 Rabbit anti-p-S6 (AB 331679) Cell Signaling Technology Shanghai, PRC 2211 WB 1:3000 Mouse anti-S6 (AB 2238583) Cell Signaling Technology Shanghai, PRC 2317 WB 1:3000 Rabbit anti-ARHGEF4 (AB 2721023) Proteintech Rosemont,IL,USA 55 213–1-AP WB 1:2000 Rabbit anti-Cingulin (AB 10733647) Proteintech Rosemont,IL,USA 21 369–1-AP IF (1:200) Rabbit anti-PRM2 (AB 2721024) Proteintech Rosemont,IL,USA 14 500–1-AP WB 1:1000 Rabbit anti-TNP1 (AB 2206757) Proteintech Rosemont,IL,USA 17 178–1-AP WB 1:1000 Mouse anti-COL1A2 (AB 2716872) Santa Cruz Biotechnolog Dallas, TX,USA SC-393 573 IF (1:100) Mouse anti-Laminin α2 (AB 1125089) Santa Cruz Biotechnolog Dallas, TX,USA SC-55 605 IF (1:100) Mouse anti-β-Actin (AB 476697) Sigma-Aldrich St. Louis, MO,USA A2228 IF (1:200) Mouse anti-α-Tubulin (AB 477582) Sigma-Aldrich St. Louis, MO,USA T6074 IF (1:200) Mouse anti-GAPDH (AB 2721026) Tianjin Sungene Biotech Tianjin, PRC KM9002 WB 1:6000 Lectin PNA, Alexa Fluor TM 488 Conjugate (AB 2315178) Thermo Fisher Scientific L21409 IF 1:100 WB, western blot; IF, immunofluorescence; IHC, immunohistochemistry.

    Immunofluorescence:

    Article Title: Raptor directs Sertoli cell cytoskeletal organization and polarity in the mouse testis.
    Article Snippet: Antibody(RRID) Vendor Catalog number Application Working Dilution for WB or (IF/IHC) Rabbit anti-Wilms Tumor1 (AB_2043201) Abcam Cambridge, MA,USA Ab89901 IF (1:200) Rabbit anti-ACTA2 (AB 2721021) ABclonal Shanghai, PRC A7248 IF (1:200) Rabbit anti-Raptor (AB 185538) Bethyl Montgomery,Alabama,USA A300–506A WB,IF 1:3000 (1:200) Rabbit anti-Vimentin (AB 1663663) Bioworld Louis Park, MN,USA BS1491 IF (1:200) Rabbit anti-Rheb (AB 2721022) Cell Signaling Technology Shanghai, PRC 13 879 WB 1:1000 Rabbit anti-Ki67 (AB 2687446) Cell Signaling Technology Shanghai, PRC 9129 IF (1:100) Rabbit anti-β-catenin (AB 331149) Cell Signaling Technology Shanghai, PRC 9562 IF (1:200) Rabbit anti-ZO1 (AB 10898025) Cell Signaling Technology Shanghai, PRC 8193 IF (1:100) Rabbit anti-ZO2 (AB 2203575) Cell Signaling Technology Shanghai, PRC 2847 IF (1:100) Rabbit anti-p-mTOR (AB 330970) Cell Signaling Technology Shanghai, PRC 2971 WB 1:1000 Rabbit anti-mTOR (AB 2105622) Cell Signaling Technology Shanghai, PRC 2983 WB 1:1000 Rabbit anti-p-p70S6K (AB 330944) Cell Signaling Technology Shanghai, PRC 9205 WB 1:2000 Rabbit anti-p70S6K (AB 390722) Cell Signaling Technology Shanghai, PRC 2708 WB 1:1000 Rabbit anti-p-S6 (AB 331679) Cell Signaling Technology Shanghai, PRC 2211 WB 1:3000 Mouse anti-S6 (AB 2238583) Cell Signaling Technology Shanghai, PRC 2317 WB 1:3000 Rabbit anti-ARHGEF4 (AB 2721023) Proteintech Rosemont,IL,USA 55 213–1-AP WB 1:2000 Rabbit anti-Cingulin (AB 10733647) Proteintech Rosemont,IL,USA 21 369–1-AP IF (1:200) Rabbit anti-PRM2 (AB 2721024) Proteintech Rosemont,IL,USA 14 500–1-AP WB 1:1000 Rabbit anti-TNP1 (AB 2206757) Proteintech Rosemont,IL,USA 17 178–1-AP WB 1:1000 Mouse anti-COL1A2 (AB 2716872) Santa Cruz Biotechnolog Dallas, TX,USA SC-393 573 IF (1:100) Mouse anti-Laminin α2 (AB 1125089) Santa Cruz Biotechnolog Dallas, TX,USA SC-55 605 IF (1:100) Mouse anti-β-Actin (AB 476697) Sigma-Aldrich St. Louis, MO,USA A2228 IF (1:200) Mouse anti-α-Tubulin (AB 477582) Sigma-Aldrich St. Louis, MO,USA T6074 IF (1:200) Mouse anti-GAPDH (AB 2721026) Tianjin Sungene Biotech Tianjin, PRC KM9002 WB 1:6000 Lectin PNA, Alexa Fluor TM 488 Conjugate (AB 2315178) Thermo Fisher Scientific L21409 IF 1:100 WB, western blot; IF, immunofluorescence; IHC, immunohistochemistry.

    Immunohistochemistry:

    Article Title: Raptor directs Sertoli cell cytoskeletal organization and polarity in the mouse testis.
    Article Snippet: Antibody(RRID) Vendor Catalog number Application Working Dilution for WB or (IF/IHC) Rabbit anti-Wilms Tumor1 (AB_2043201) Abcam Cambridge, MA,USA Ab89901 IF (1:200) Rabbit anti-ACTA2 (AB 2721021) ABclonal Shanghai, PRC A7248 IF (1:200) Rabbit anti-Raptor (AB 185538) Bethyl Montgomery,Alabama,USA A300–506A WB,IF 1:3000 (1:200) Rabbit anti-Vimentin (AB 1663663) Bioworld Louis Park, MN,USA BS1491 IF (1:200) Rabbit anti-Rheb (AB 2721022) Cell Signaling Technology Shanghai, PRC 13 879 WB 1:1000 Rabbit anti-Ki67 (AB 2687446) Cell Signaling Technology Shanghai, PRC 9129 IF (1:100) Rabbit anti-β-catenin (AB 331149) Cell Signaling Technology Shanghai, PRC 9562 IF (1:200) Rabbit anti-ZO1 (AB 10898025) Cell Signaling Technology Shanghai, PRC 8193 IF (1:100) Rabbit anti-ZO2 (AB 2203575) Cell Signaling Technology Shanghai, PRC 2847 IF (1:100) Rabbit anti-p-mTOR (AB 330970) Cell Signaling Technology Shanghai, PRC 2971 WB 1:1000 Rabbit anti-mTOR (AB 2105622) Cell Signaling Technology Shanghai, PRC 2983 WB 1:1000 Rabbit anti-p-p70S6K (AB 330944) Cell Signaling Technology Shanghai, PRC 9205 WB 1:2000 Rabbit anti-p70S6K (AB 390722) Cell Signaling Technology Shanghai, PRC 2708 WB 1:1000 Rabbit anti-p-S6 (AB 331679) Cell Signaling Technology Shanghai, PRC 2211 WB 1:3000 Mouse anti-S6 (AB 2238583) Cell Signaling Technology Shanghai, PRC 2317 WB 1:3000 Rabbit anti-ARHGEF4 (AB 2721023) Proteintech Rosemont,IL,USA 55 213–1-AP WB 1:2000 Rabbit anti-Cingulin (AB 10733647) Proteintech Rosemont,IL,USA 21 369–1-AP IF (1:200) Rabbit anti-PRM2 (AB 2721024) Proteintech Rosemont,IL,USA 14 500–1-AP WB 1:1000 Rabbit anti-TNP1 (AB 2206757) Proteintech Rosemont,IL,USA 17 178–1-AP WB 1:1000 Mouse anti-COL1A2 (AB 2716872) Santa Cruz Biotechnolog Dallas, TX,USA SC-393 573 IF (1:100) Mouse anti-Laminin α2 (AB 1125089) Santa Cruz Biotechnolog Dallas, TX,USA SC-55 605 IF (1:100) Mouse anti-β-Actin (AB 476697) Sigma-Aldrich St. Louis, MO,USA A2228 IF (1:200) Mouse anti-α-Tubulin (AB 477582) Sigma-Aldrich St. Louis, MO,USA T6074 IF (1:200) Mouse anti-GAPDH (AB 2721026) Tianjin Sungene Biotech Tianjin, PRC KM9002 WB 1:6000 Lectin PNA, Alexa Fluor TM 488 Conjugate (AB 2315178) Thermo Fisher Scientific L21409 IF 1:100 WB, western blot; IF, immunofluorescence; IHC, immunohistochemistry.



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    Transcriptome analysis in human spinal cord organoids (hSCOs) exposed to valproic acid (VPA). (A) Scatter plots of transcriptome levels in hSCOs treated with VPA compared with the controls. Red circles denote the genes whose expression levels were significantly altered (≥2-fold) in VPA-treated vs control groups. (B) Biological processes associated with significantly upregulated genes. (C) Network plot of the upregulated genes enriched in VPA-treated hSCOs. Interactive network is generated using GeneMANIA plugin in Cytoscape. (D) Immunohistochemical evaluation of the upregulation of tight junction proteins, Occludin (OCLN), and <t>ZO2.</t> Average intensity of tight junction proteins was measured along the apico-basal axis. Scale bar=20 μm. (E) Perturbation of polarized localization of ZO1 and pMLC proteins in the neuroepithelial cells of VPA-treated hSCOs. White arrows indicate the ectopic expression of proteins in the VPA-treated group. Bar graphs show the number of ectopic ZO1 and pMLC punctas in neural-plate layers. Unpaired Student’s t-test was used for comparing two groups (**p<0.01 and ***p<0.01). Scale bar=20 μm. FC: fold change, Ctrl: control.
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    Transcriptome analysis in human spinal cord organoids (hSCOs) exposed to valproic acid (VPA). (A) Scatter plots of transcriptome levels in hSCOs treated with VPA compared with the controls. Red circles denote the genes whose expression levels were significantly altered (≥2-fold) in VPA-treated vs control groups. (B) Biological processes associated with significantly upregulated genes. (C) Network plot of the upregulated genes enriched in VPA-treated hSCOs. Interactive network is generated using GeneMANIA plugin in Cytoscape. (D) Immunohistochemical evaluation of the upregulation of tight junction proteins, Occludin (OCLN), and <t>ZO2.</t> Average intensity of tight junction proteins was measured along the apico-basal axis. Scale bar=20 μm. (E) Perturbation of polarized localization of ZO1 and pMLC proteins in the neuroepithelial cells of VPA-treated hSCOs. White arrows indicate the ectopic expression of proteins in the VPA-treated group. Bar graphs show the number of ectopic ZO1 and pMLC punctas in neural-plate layers. Unpaired Student’s t-test was used for comparing two groups (**p<0.01 and ***p<0.01). Scale bar=20 μm. FC: fold change, Ctrl: control.
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    Image Search Results


    Transcriptome analysis in human spinal cord organoids (hSCOs) exposed to valproic acid (VPA). (A) Scatter plots of transcriptome levels in hSCOs treated with VPA compared with the controls. Red circles denote the genes whose expression levels were significantly altered (≥2-fold) in VPA-treated vs control groups. (B) Biological processes associated with significantly upregulated genes. (C) Network plot of the upregulated genes enriched in VPA-treated hSCOs. Interactive network is generated using GeneMANIA plugin in Cytoscape. (D) Immunohistochemical evaluation of the upregulation of tight junction proteins, Occludin (OCLN), and ZO2. Average intensity of tight junction proteins was measured along the apico-basal axis. Scale bar=20 μm. (E) Perturbation of polarized localization of ZO1 and pMLC proteins in the neuroepithelial cells of VPA-treated hSCOs. White arrows indicate the ectopic expression of proteins in the VPA-treated group. Bar graphs show the number of ectopic ZO1 and pMLC punctas in neural-plate layers. Unpaired Student’s t-test was used for comparing two groups (**p<0.01 and ***p<0.01). Scale bar=20 μm. FC: fold change, Ctrl: control.

    Journal: International Journal of Stem Cells

    Article Title: Transcriptional Signature of Valproic Acid-Induced Neural Tube Defects in Human Spinal Cord Organoids

    doi: 10.15283/ijsc23012

    Figure Lengend Snippet: Transcriptome analysis in human spinal cord organoids (hSCOs) exposed to valproic acid (VPA). (A) Scatter plots of transcriptome levels in hSCOs treated with VPA compared with the controls. Red circles denote the genes whose expression levels were significantly altered (≥2-fold) in VPA-treated vs control groups. (B) Biological processes associated with significantly upregulated genes. (C) Network plot of the upregulated genes enriched in VPA-treated hSCOs. Interactive network is generated using GeneMANIA plugin in Cytoscape. (D) Immunohistochemical evaluation of the upregulation of tight junction proteins, Occludin (OCLN), and ZO2. Average intensity of tight junction proteins was measured along the apico-basal axis. Scale bar=20 μm. (E) Perturbation of polarized localization of ZO1 and pMLC proteins in the neuroepithelial cells of VPA-treated hSCOs. White arrows indicate the ectopic expression of proteins in the VPA-treated group. Bar graphs show the number of ectopic ZO1 and pMLC punctas in neural-plate layers. Unpaired Student’s t-test was used for comparing two groups (**p<0.01 and ***p<0.01). Scale bar=20 μm. FC: fold change, Ctrl: control.

    Article Snippet: The antibodies used in this study were as follows: mouse anti-ZO1 (1:250, 33-9100; Invitrogen), rabbit anti-ZO2 (1:250, 71-1400; Invitrogen), and goat anti-SOX2 (1:250, sc-17320; Santa Cruz).

    Techniques: Expressing, Generated, Immunohistochemistry

    Effect of tight junction proteins expression/distribution in valproic acid (VPA)-treated human spinal cord or-ganoid. (A) Immunohistochemistry of upregulation of tight junction proteins, ZO2 (red) and ZO1 (green) caused by VPA treatments for different durations. Scale bar=10 μm. (B) Line plots denoting the intensity of ZO1 and ZO2 staining along the closed/opened neural tube. (C) Pertur-bation of polarized localization of ZO1 proteins in neuroepithelium. The neuroepithelial cells were identified as SOX2 (magenta) staining and cellular arrangement surrounding apical marker, ZO1 (green). Scale bar=10 μm. (D) Quantification of the number of ectopic ZO1 punctas within neuroepithelial cell layers. Bar graphs represent mean±SEM, with all the points plotted. Unpaired Student’s t-test was used for comparing two groups (*p<0.05).

    Journal: International Journal of Stem Cells

    Article Title: Transcriptional Signature of Valproic Acid-Induced Neural Tube Defects in Human Spinal Cord Organoids

    doi: 10.15283/ijsc23012

    Figure Lengend Snippet: Effect of tight junction proteins expression/distribution in valproic acid (VPA)-treated human spinal cord or-ganoid. (A) Immunohistochemistry of upregulation of tight junction proteins, ZO2 (red) and ZO1 (green) caused by VPA treatments for different durations. Scale bar=10 μm. (B) Line plots denoting the intensity of ZO1 and ZO2 staining along the closed/opened neural tube. (C) Pertur-bation of polarized localization of ZO1 proteins in neuroepithelium. The neuroepithelial cells were identified as SOX2 (magenta) staining and cellular arrangement surrounding apical marker, ZO1 (green). Scale bar=10 μm. (D) Quantification of the number of ectopic ZO1 punctas within neuroepithelial cell layers. Bar graphs represent mean±SEM, with all the points plotted. Unpaired Student’s t-test was used for comparing two groups (*p<0.05).

    Article Snippet: The antibodies used in this study were as follows: mouse anti-ZO1 (1:250, 33-9100; Invitrogen), rabbit anti-ZO2 (1:250, 71-1400; Invitrogen), and goat anti-SOX2 (1:250, sc-17320; Santa Cruz).

    Techniques: Expressing, Immunohistochemistry, Staining, Marker

    Effect of valproic acid (VPA) on neural tube in the mouse em-bryo. Immunohistochemistry of VPA-induced neural tube defect mouse models. Various markers were used to observe changes in the expre-ssion/distribution of actin filaments (A, F-actin and pMLC) and tight junction proteins (B, Zo1, Zo2, and Ocln). Dissolved VPA was administrated three times to pregnant female mice at the time of primary neuru-lation. Scale bars=20 μm. Min: minimum, Max: maximum.

    Journal: International Journal of Stem Cells

    Article Title: Transcriptional Signature of Valproic Acid-Induced Neural Tube Defects in Human Spinal Cord Organoids

    doi: 10.15283/ijsc23012

    Figure Lengend Snippet: Effect of valproic acid (VPA) on neural tube in the mouse em-bryo. Immunohistochemistry of VPA-induced neural tube defect mouse models. Various markers were used to observe changes in the expre-ssion/distribution of actin filaments (A, F-actin and pMLC) and tight junction proteins (B, Zo1, Zo2, and Ocln). Dissolved VPA was administrated three times to pregnant female mice at the time of primary neuru-lation. Scale bars=20 μm. Min: minimum, Max: maximum.

    Article Snippet: The antibodies used in this study were as follows: mouse anti-ZO1 (1:250, 33-9100; Invitrogen), rabbit anti-ZO2 (1:250, 71-1400; Invitrogen), and goat anti-SOX2 (1:250, sc-17320; Santa Cruz).

    Techniques: Immunohistochemistry