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antirabbit tomm40 antibody  (Proteintech)


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    Proteintech antirabbit tomm40 antibody
    Figure 7. BRG1 induces the expession of <t>TOMM40</t> in HCC cells. (a) HepG2 cells were stained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. (b and c) the percentage of positive cells was analyzed by ImageJ software (n = 10). **p < .01, ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (d) HuH-7 cells were stained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. (e and f) the percentage of positive cells was analyzed by ImageJ software (n = 10). ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC.
    Antirabbit Tomm40 Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 167 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/antirabbit+tomm40+antibody/TOMM40+Antibody/pm38978225-30-27-32
    Average 96 stars, based on 167 article reviews
    antirabbit tomm40 antibody - by Bioz Stars, 2026-09
    96/100 stars

    Images

    1) Product Images from "BRG1 promotes liver cancer cell proliferation and metastasis by enhancing mitochondrial function and ATP5A1 synthesis through TOMM40."

    Article Title: BRG1 promotes liver cancer cell proliferation and metastasis by enhancing mitochondrial function and ATP5A1 synthesis through TOMM40.

    Journal: Cancer biology & therapy

    doi: 10.1080/15384047.2024.2375440

    Figure 7. BRG1 induces the expession of TOMM40 in HCC cells. (a) HepG2 cells were stained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. (b and c) the percentage of positive cells was analyzed by ImageJ software (n = 10). **p < .01, ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (d) HuH-7 cells were stained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. (e and f) the percentage of positive cells was analyzed by ImageJ software (n = 10). ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC.
    Figure Legend Snippet: Figure 7. BRG1 induces the expession of TOMM40 in HCC cells. (a) HepG2 cells were stained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. (b and c) the percentage of positive cells was analyzed by ImageJ software (n = 10). **p < .01, ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (d) HuH-7 cells were stained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. (e and f) the percentage of positive cells was analyzed by ImageJ software (n = 10). ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC.

    Techniques Used: Staining, Knockdown, Over Expression, Software

    Figure 8. BRG1 induces the expession of TOMM40 in HCC cells. (a) HepG2 cells were immunostained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. Scale bar, 20 μm. (b and c) the relative fluorescence intensity was analyzed by ImageJ software (n = 10). ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (d) HuH-7 cells were immunostained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. Scale bar, 20 μm. (e and f) the relative fluorescence intensity was analyzed by Image J software (n = 10). ***p < .001 vs siRNA-NC, ###p < .001 vs pcDNA3.1-NC.
    Figure Legend Snippet: Figure 8. BRG1 induces the expession of TOMM40 in HCC cells. (a) HepG2 cells were immunostained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. Scale bar, 20 μm. (b and c) the relative fluorescence intensity was analyzed by ImageJ software (n = 10). ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (d) HuH-7 cells were immunostained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. Scale bar, 20 μm. (e and f) the relative fluorescence intensity was analyzed by Image J software (n = 10). ***p < .001 vs siRNA-NC, ###p < .001 vs pcDNA3.1-NC.

    Techniques Used: Knockdown, Over Expression, Fluorescence, Software

    Figure 9. BRG1 activates TOMM40/ATP5A1 pathway in HCC cells. (a) The expressions of BRG1, TOMM40 and ATP5A1 were analyzed using Western blotting after BRG1 knockdown or overexpression in HepG2 cells. (b-d) the relative intensities of BRG1, TOMM40 and ATP5A1 were determined using ImageJ software (n = 3). **p < .01, ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (e) The expressions of BRG1, TOMM40 and ATP5A1 were analyzed using Western blotting after BRG1 knockdown or overexpression in HuH-7 cells. (f-h) the relative intensity were determined using ImageJ software (n = 3). **p < .01, ***p < .001 vs siRNA-NC, ###p < .001 vs pcDNA3.1-NC. (i-l) the mRNA expressions level of BRG1, TOMM40 and ATP5A1 were analyzed using RT-qPCR.(n = 3). ##p < .01, ###p < .001 vs siRNA-NC, ***p < .001 vs pcDNA3.1-NC.
    Figure Legend Snippet: Figure 9. BRG1 activates TOMM40/ATP5A1 pathway in HCC cells. (a) The expressions of BRG1, TOMM40 and ATP5A1 were analyzed using Western blotting after BRG1 knockdown or overexpression in HepG2 cells. (b-d) the relative intensities of BRG1, TOMM40 and ATP5A1 were determined using ImageJ software (n = 3). **p < .01, ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (e) The expressions of BRG1, TOMM40 and ATP5A1 were analyzed using Western blotting after BRG1 knockdown or overexpression in HuH-7 cells. (f-h) the relative intensity were determined using ImageJ software (n = 3). **p < .01, ***p < .001 vs siRNA-NC, ###p < .001 vs pcDNA3.1-NC. (i-l) the mRNA expressions level of BRG1, TOMM40 and ATP5A1 were analyzed using RT-qPCR.(n = 3). ##p < .01, ###p < .001 vs siRNA-NC, ***p < .001 vs pcDNA3.1-NC.

    Techniques Used: Western Blot, Knockdown, Over Expression, Software, Quantitative RT-PCR

    Related Articles

    Blocking Assay:

    Article Title: BRG1 promotes liver cancer cell proliferation and metastasis by enhancing mitochondrial function and ATP5A1 synthesis through TOMM40.
    Article Snippet: Equal amounts of 30 μg protein were separated in an 8%~10% SDS-PAGE gel and transferred to a PVDF membrane (Cat#IPVH00010, Millipore). .. After blocking with 5% nonfat milk for 1 h at room temperature, the membranes were incubated with indicated primary antibodies: anti-rabbit BRG1 antibody (1:1000, 21634–1-AP, Proteintech, China), antirabbit TOMM40 antibody (1:1000, 18409–1-AP, Proteintech, China), anti-rabbit ATP5A1 (1:1000, 14676–1-AP, Proteintech, China) and anti-mouse β-actin antibody (1:2000, 66009–1-Ig, Proteintech, China) overnight at 4°C. .. Then, the blots were incubated with HRP-conjugated goat anti-rabbit or mouse IgG secondary antibody (1:6000, Cat# SA00001–2, Proteintech, China) for 1 h and were exposed in the SuperSignal West Pico Substrate (Cat#D3308–1, Beyotime Biotech).

    Incubation:

    Article Title: BRG1 promotes liver cancer cell proliferation and metastasis by enhancing mitochondrial function and ATP5A1 synthesis through TOMM40.
    Article Snippet: Equal amounts of 30 μg protein were separated in an 8%~10% SDS-PAGE gel and transferred to a PVDF membrane (Cat#IPVH00010, Millipore). .. After blocking with 5% nonfat milk for 1 h at room temperature, the membranes were incubated with indicated primary antibodies: anti-rabbit BRG1 antibody (1:1000, 21634–1-AP, Proteintech, China), antirabbit TOMM40 antibody (1:1000, 18409–1-AP, Proteintech, China), anti-rabbit ATP5A1 (1:1000, 14676–1-AP, Proteintech, China) and anti-mouse β-actin antibody (1:2000, 66009–1-Ig, Proteintech, China) overnight at 4°C. .. Then, the blots were incubated with HRP-conjugated goat anti-rabbit or mouse IgG secondary antibody (1:6000, Cat# SA00001–2, Proteintech, China) for 1 h and were exposed in the SuperSignal West Pico Substrate (Cat#D3308–1, Beyotime Biotech).



    Similar Products

    antirabbit tomm40 antibody  (Proteintech)
    96
    Proteintech antirabbit tomm40 antibody
    Figure 7. BRG1 induces the expession of <t>TOMM40</t> in HCC cells. (a) HepG2 cells were stained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. (b and c) the percentage of positive cells was analyzed by ImageJ software (n = 10). **p < .01, ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (d) HuH-7 cells were stained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. (e and f) the percentage of positive cells was analyzed by ImageJ software (n = 10). ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC.
    Antirabbit Tomm40 Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/antirabbit+tomm40+antibody/TOMM40+Antibody/pm38978225-30-27-32
    Average 96 stars, based on 1 article reviews
    antirabbit tomm40 antibody - by Bioz Stars, 2026-09
    96/100 stars
    		  Buy from Supplier

    Image Search Results


    Figure 7. BRG1 induces the expession of TOMM40 in HCC cells. (a) HepG2 cells were stained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. (b and c) the percentage of positive cells was analyzed by ImageJ software (n = 10). **p < .01, ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (d) HuH-7 cells were stained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. (e and f) the percentage of positive cells was analyzed by ImageJ software (n = 10). ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC.

    Journal: Cancer biology & therapy

    Article Title: BRG1 promotes liver cancer cell proliferation and metastasis by enhancing mitochondrial function and ATP5A1 synthesis through TOMM40.

    doi: 10.1080/15384047.2024.2375440

    Figure Lengend Snippet: Figure 7. BRG1 induces the expession of TOMM40 in HCC cells. (a) HepG2 cells were stained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. (b and c) the percentage of positive cells was analyzed by ImageJ software (n = 10). **p < .01, ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (d) HuH-7 cells were stained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. (e and f) the percentage of positive cells was analyzed by ImageJ software (n = 10). ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC.

    Article Snippet: After blocking with 5% nonfat milk for 1 h at room temperature, the membranes were incubated with indicated primary antibodies: anti-rabbit BRG1 antibody (1:1000, 21634–1-AP, Proteintech, China), antirabbit TOMM40 antibody (1:1000, 18409–1-AP, Proteintech, China), anti-rabbit ATP5A1 (1:1000, 14676–1-AP, Proteintech, China) and anti-mouse β-actin antibody (1:2000, 66009–1-Ig, Proteintech, China) overnight at 4°C.

    Techniques: Staining, Knockdown, Over Expression, Software

    Figure 8. BRG1 induces the expession of TOMM40 in HCC cells. (a) HepG2 cells were immunostained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. Scale bar, 20 μm. (b and c) the relative fluorescence intensity was analyzed by ImageJ software (n = 10). ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (d) HuH-7 cells were immunostained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. Scale bar, 20 μm. (e and f) the relative fluorescence intensity was analyzed by Image J software (n = 10). ***p < .001 vs siRNA-NC, ###p < .001 vs pcDNA3.1-NC.

    Journal: Cancer biology & therapy

    Article Title: BRG1 promotes liver cancer cell proliferation and metastasis by enhancing mitochondrial function and ATP5A1 synthesis through TOMM40.

    doi: 10.1080/15384047.2024.2375440

    Figure Lengend Snippet: Figure 8. BRG1 induces the expession of TOMM40 in HCC cells. (a) HepG2 cells were immunostained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. Scale bar, 20 μm. (b and c) the relative fluorescence intensity was analyzed by ImageJ software (n = 10). ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (d) HuH-7 cells were immunostained with TOMM40 and BRG1 antibody after BRG1 knockdown or overexpression. Scale bar, 20 μm. (e and f) the relative fluorescence intensity was analyzed by Image J software (n = 10). ***p < .001 vs siRNA-NC, ###p < .001 vs pcDNA3.1-NC.

    Article Snippet: After blocking with 5% nonfat milk for 1 h at room temperature, the membranes were incubated with indicated primary antibodies: anti-rabbit BRG1 antibody (1:1000, 21634–1-AP, Proteintech, China), antirabbit TOMM40 antibody (1:1000, 18409–1-AP, Proteintech, China), anti-rabbit ATP5A1 (1:1000, 14676–1-AP, Proteintech, China) and anti-mouse β-actin antibody (1:2000, 66009–1-Ig, Proteintech, China) overnight at 4°C.

    Techniques: Knockdown, Over Expression, Fluorescence, Software

    Figure 9. BRG1 activates TOMM40/ATP5A1 pathway in HCC cells. (a) The expressions of BRG1, TOMM40 and ATP5A1 were analyzed using Western blotting after BRG1 knockdown or overexpression in HepG2 cells. (b-d) the relative intensities of BRG1, TOMM40 and ATP5A1 were determined using ImageJ software (n = 3). **p < .01, ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (e) The expressions of BRG1, TOMM40 and ATP5A1 were analyzed using Western blotting after BRG1 knockdown or overexpression in HuH-7 cells. (f-h) the relative intensity were determined using ImageJ software (n = 3). **p < .01, ***p < .001 vs siRNA-NC, ###p < .001 vs pcDNA3.1-NC. (i-l) the mRNA expressions level of BRG1, TOMM40 and ATP5A1 were analyzed using RT-qPCR.(n = 3). ##p < .01, ###p < .001 vs siRNA-NC, ***p < .001 vs pcDNA3.1-NC.

    Journal: Cancer biology & therapy

    Article Title: BRG1 promotes liver cancer cell proliferation and metastasis by enhancing mitochondrial function and ATP5A1 synthesis through TOMM40.

    doi: 10.1080/15384047.2024.2375440

    Figure Lengend Snippet: Figure 9. BRG1 activates TOMM40/ATP5A1 pathway in HCC cells. (a) The expressions of BRG1, TOMM40 and ATP5A1 were analyzed using Western blotting after BRG1 knockdown or overexpression in HepG2 cells. (b-d) the relative intensities of BRG1, TOMM40 and ATP5A1 were determined using ImageJ software (n = 3). **p < .01, ***p < .001 vs siRNA-NC, ##p < .01, ###p < .001 vs pcDNA3.1-NC. (e) The expressions of BRG1, TOMM40 and ATP5A1 were analyzed using Western blotting after BRG1 knockdown or overexpression in HuH-7 cells. (f-h) the relative intensity were determined using ImageJ software (n = 3). **p < .01, ***p < .001 vs siRNA-NC, ###p < .001 vs pcDNA3.1-NC. (i-l) the mRNA expressions level of BRG1, TOMM40 and ATP5A1 were analyzed using RT-qPCR.(n = 3). ##p < .01, ###p < .001 vs siRNA-NC, ***p < .001 vs pcDNA3.1-NC.

    Article Snippet: After blocking with 5% nonfat milk for 1 h at room temperature, the membranes were incubated with indicated primary antibodies: anti-rabbit BRG1 antibody (1:1000, 21634–1-AP, Proteintech, China), antirabbit TOMM40 antibody (1:1000, 18409–1-AP, Proteintech, China), anti-rabbit ATP5A1 (1:1000, 14676–1-AP, Proteintech, China) and anti-mouse β-actin antibody (1:2000, 66009–1-Ig, Proteintech, China) overnight at 4°C.

    Techniques: Western Blot, Knockdown, Over Expression, Software, Quantitative RT-PCR