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anti gpihbp1  (Novus Biologicals)


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    Structured Review

    Novus Biologicals anti gpihbp1
    Anti Gpihbp1, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/anti gpihbp1/product/Novus Biologicals
    Average 94 stars, based on 1 article reviews
    anti gpihbp1 - by Bioz Stars, 2026-05
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    Novus Biologicals trpa1
    Calcium imaging and immunocytochemistry showing TRPV1 expression in transfected HEK‐293 cells. (A) Fura2 calcium imaging in HEK‐293 cells transiently expressing rTRPV1‐EYFP fusion protein. Representative traces of calcium transients evoked by capsaicin in EYFP + cells. Green traces correspond to EYFP + cells and gray traces to EYFP − cells. Pie chart represents the percentage of EYFP + cells that responded or failded to respond to capsaicin. Data obtained from 88 cells from 3 coverslips. (B–F left) Confocal images of TRPV1‐EYFP transiently expressed in HEK‐293 cells. EYFP (green), TRPV1 antibody (magenta) and Hoechst (HO, blue). Merge images correspond to the overlap between TRPV1 and EYFP on the left and Hoechst and brightfield (BF) on the right. Antibody dilution of the representative images is indicated in the lower right corner. Scale bar: 20 μm. (B–F right) Box plots display the specificity ratio (SR) for each tested dilution of the corresponding antibody. Each dot represents a single EYFP + cell. Boxes indicate the interquartile range (25th to 75th percentiles) and whiskers extend to the 5th and 95th percentiles. The horizontal line inside each box marks the median and the black dot indicates the mean. (*** p < 0.001 Mann–Whitney test). (G) Bar histogram graph summarizes the SR median difference between the tested antibody dilution and their controls lacking primary antibody (secondary antibody only; rabbit, goat or guinea pig) as calculated with the Hodges‐Lehman estimator. Error bars represent the 95% confidence interval. For each antibody and dilution, a minimum of 100 cells were analyzed across 4 fields from 2 independent transfections. $ Santa Cruz V1 antibody was generated against a human <t>TRPA1</t> peptide.
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    Calcium imaging and immunocytochemistry showing TRPV1 expression in transfected HEK‐293 cells. (A) Fura2 calcium imaging in HEK‐293 cells transiently expressing rTRPV1‐EYFP fusion protein. Representative traces of calcium transients evoked by capsaicin in EYFP + cells. Green traces correspond to EYFP + cells and gray traces to EYFP − cells. Pie chart represents the percentage of EYFP + cells that responded or failded to respond to capsaicin. Data obtained from 88 cells from 3 coverslips. (B–F left) Confocal images of TRPV1‐EYFP transiently expressed in HEK‐293 cells. EYFP (green), TRPV1 antibody (magenta) and Hoechst (HO, blue). Merge images correspond to the overlap between TRPV1 and EYFP on the left and Hoechst and brightfield (BF) on the right. Antibody dilution of the representative images is indicated in the lower right corner. Scale bar: 20 μm. (B–F right) Box plots display the specificity ratio (SR) for each tested dilution of the corresponding antibody. Each dot represents a single EYFP + cell. Boxes indicate the interquartile range (25th to 75th percentiles) and whiskers extend to the 5th and 95th percentiles. The horizontal line inside each box marks the median and the black dot indicates the mean. (*** p < 0.001 Mann–Whitney test). (G) Bar histogram graph summarizes the SR median difference between the tested antibody dilution and their controls lacking primary antibody (secondary antibody only; rabbit, goat or guinea pig) as calculated with the Hodges‐Lehman estimator. Error bars represent the 95% confidence interval. For each antibody and dilution, a minimum of 100 cells were analyzed across 4 fields from 2 independent transfections. $ Santa Cruz V1 antibody was generated against a human <t>TRPA1</t> peptide.
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    Novus Biologicals optic atrophy 1 opa1
    Calcium imaging and immunocytochemistry showing TRPV1 expression in transfected HEK‐293 cells. (A) Fura2 calcium imaging in HEK‐293 cells transiently expressing rTRPV1‐EYFP fusion protein. Representative traces of calcium transients evoked by capsaicin in EYFP + cells. Green traces correspond to EYFP + cells and gray traces to EYFP − cells. Pie chart represents the percentage of EYFP + cells that responded or failded to respond to capsaicin. Data obtained from 88 cells from 3 coverslips. (B–F left) Confocal images of TRPV1‐EYFP transiently expressed in HEK‐293 cells. EYFP (green), TRPV1 antibody (magenta) and Hoechst (HO, blue). Merge images correspond to the overlap between TRPV1 and EYFP on the left and Hoechst and brightfield (BF) on the right. Antibody dilution of the representative images is indicated in the lower right corner. Scale bar: 20 μm. (B–F right) Box plots display the specificity ratio (SR) for each tested dilution of the corresponding antibody. Each dot represents a single EYFP + cell. Boxes indicate the interquartile range (25th to 75th percentiles) and whiskers extend to the 5th and 95th percentiles. The horizontal line inside each box marks the median and the black dot indicates the mean. (*** p < 0.001 Mann–Whitney test). (G) Bar histogram graph summarizes the SR median difference between the tested antibody dilution and their controls lacking primary antibody (secondary antibody only; rabbit, goat or guinea pig) as calculated with the Hodges‐Lehman estimator. Error bars represent the 95% confidence interval. For each antibody and dilution, a minimum of 100 cells were analyzed across 4 fields from 2 independent transfections. $ Santa Cruz V1 antibody was generated against a human <t>TRPA1</t> peptide.
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    Calcium imaging and immunocytochemistry showing TRPV1 expression in transfected HEK‐293 cells. (A) Fura2 calcium imaging in HEK‐293 cells transiently expressing rTRPV1‐EYFP fusion protein. Representative traces of calcium transients evoked by capsaicin in EYFP + cells. Green traces correspond to EYFP + cells and gray traces to EYFP − cells. Pie chart represents the percentage of EYFP + cells that responded or failded to respond to capsaicin. Data obtained from 88 cells from 3 coverslips. (B–F left) Confocal images of TRPV1‐EYFP transiently expressed in HEK‐293 cells. EYFP (green), TRPV1 antibody (magenta) and Hoechst (HO, blue). Merge images correspond to the overlap between TRPV1 and EYFP on the left and Hoechst and brightfield (BF) on the right. Antibody dilution of the representative images is indicated in the lower right corner. Scale bar: 20 μm. (B–F right) Box plots display the specificity ratio (SR) for each tested dilution of the corresponding antibody. Each dot represents a single EYFP + cell. Boxes indicate the interquartile range (25th to 75th percentiles) and whiskers extend to the 5th and 95th percentiles. The horizontal line inside each box marks the median and the black dot indicates the mean. (*** p < 0.001 Mann–Whitney test). (G) Bar histogram graph summarizes the SR median difference between the tested antibody dilution and their controls lacking primary antibody (secondary antibody only; rabbit, goat or guinea pig) as calculated with the Hodges‐Lehman estimator. Error bars represent the 95% confidence interval. For each antibody and dilution, a minimum of 100 cells were analyzed across 4 fields from 2 independent transfections. $ Santa Cruz V1 antibody was generated against a human <t>TRPA1</t> peptide.
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    Novus Biologicals mouse monoclonal antibodies against tas2r3
    Calcium imaging and immunocytochemistry showing TRPV1 expression in transfected HEK‐293 cells. (A) Fura2 calcium imaging in HEK‐293 cells transiently expressing rTRPV1‐EYFP fusion protein. Representative traces of calcium transients evoked by capsaicin in EYFP + cells. Green traces correspond to EYFP + cells and gray traces to EYFP − cells. Pie chart represents the percentage of EYFP + cells that responded or failded to respond to capsaicin. Data obtained from 88 cells from 3 coverslips. (B–F left) Confocal images of TRPV1‐EYFP transiently expressed in HEK‐293 cells. EYFP (green), TRPV1 antibody (magenta) and Hoechst (HO, blue). Merge images correspond to the overlap between TRPV1 and EYFP on the left and Hoechst and brightfield (BF) on the right. Antibody dilution of the representative images is indicated in the lower right corner. Scale bar: 20 μm. (B–F right) Box plots display the specificity ratio (SR) for each tested dilution of the corresponding antibody. Each dot represents a single EYFP + cell. Boxes indicate the interquartile range (25th to 75th percentiles) and whiskers extend to the 5th and 95th percentiles. The horizontal line inside each box marks the median and the black dot indicates the mean. (*** p < 0.001 Mann–Whitney test). (G) Bar histogram graph summarizes the SR median difference between the tested antibody dilution and their controls lacking primary antibody (secondary antibody only; rabbit, goat or guinea pig) as calculated with the Hodges‐Lehman estimator. Error bars represent the 95% confidence interval. For each antibody and dilution, a minimum of 100 cells were analyzed across 4 fields from 2 independent transfections. $ Santa Cruz V1 antibody was generated against a human <t>TRPA1</t> peptide.
    Mouse Monoclonal Antibodies Against Tas2r3, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Novus Biologicals rabbit polyclonal antibody against tas2r4
    Calcium imaging and immunocytochemistry showing TRPV1 expression in transfected HEK‐293 cells. (A) Fura2 calcium imaging in HEK‐293 cells transiently expressing rTRPV1‐EYFP fusion protein. Representative traces of calcium transients evoked by capsaicin in EYFP + cells. Green traces correspond to EYFP + cells and gray traces to EYFP − cells. Pie chart represents the percentage of EYFP + cells that responded or failded to respond to capsaicin. Data obtained from 88 cells from 3 coverslips. (B–F left) Confocal images of TRPV1‐EYFP transiently expressed in HEK‐293 cells. EYFP (green), TRPV1 antibody (magenta) and Hoechst (HO, blue). Merge images correspond to the overlap between TRPV1 and EYFP on the left and Hoechst and brightfield (BF) on the right. Antibody dilution of the representative images is indicated in the lower right corner. Scale bar: 20 μm. (B–F right) Box plots display the specificity ratio (SR) for each tested dilution of the corresponding antibody. Each dot represents a single EYFP + cell. Boxes indicate the interquartile range (25th to 75th percentiles) and whiskers extend to the 5th and 95th percentiles. The horizontal line inside each box marks the median and the black dot indicates the mean. (*** p < 0.001 Mann–Whitney test). (G) Bar histogram graph summarizes the SR median difference between the tested antibody dilution and their controls lacking primary antibody (secondary antibody only; rabbit, goat or guinea pig) as calculated with the Hodges‐Lehman estimator. Error bars represent the 95% confidence interval. For each antibody and dilution, a minimum of 100 cells were analyzed across 4 fields from 2 independent transfections. $ Santa Cruz V1 antibody was generated against a human <t>TRPA1</t> peptide.
    Rabbit Polyclonal Antibody Against Tas2r4, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Novus Biologicals cox4
    mtSTAT3 regulates mitochondrial function and fibrosis in human intestinal cells. Overexpression of mtSTAT3 reduced the fibrosis marker C18. (A) Lysates of C18 cells transfected with mock and mtSTAT3 overexpression vector were analyzed for mtSTAT3 protein in mitochondria by Western blotting. (B, C) mRNA levels of the OXPHOS complex genes <t>COX4</t> and ATP5O and the fibrosis genes aSMA, fibronectin, and COL1A1 according to real-time PCR.
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    Image Search Results


    Calcium imaging and immunocytochemistry showing TRPV1 expression in transfected HEK‐293 cells. (A) Fura2 calcium imaging in HEK‐293 cells transiently expressing rTRPV1‐EYFP fusion protein. Representative traces of calcium transients evoked by capsaicin in EYFP + cells. Green traces correspond to EYFP + cells and gray traces to EYFP − cells. Pie chart represents the percentage of EYFP + cells that responded or failded to respond to capsaicin. Data obtained from 88 cells from 3 coverslips. (B–F left) Confocal images of TRPV1‐EYFP transiently expressed in HEK‐293 cells. EYFP (green), TRPV1 antibody (magenta) and Hoechst (HO, blue). Merge images correspond to the overlap between TRPV1 and EYFP on the left and Hoechst and brightfield (BF) on the right. Antibody dilution of the representative images is indicated in the lower right corner. Scale bar: 20 μm. (B–F right) Box plots display the specificity ratio (SR) for each tested dilution of the corresponding antibody. Each dot represents a single EYFP + cell. Boxes indicate the interquartile range (25th to 75th percentiles) and whiskers extend to the 5th and 95th percentiles. The horizontal line inside each box marks the median and the black dot indicates the mean. (*** p < 0.001 Mann–Whitney test). (G) Bar histogram graph summarizes the SR median difference between the tested antibody dilution and their controls lacking primary antibody (secondary antibody only; rabbit, goat or guinea pig) as calculated with the Hodges‐Lehman estimator. Error bars represent the 95% confidence interval. For each antibody and dilution, a minimum of 100 cells were analyzed across 4 fields from 2 independent transfections. $ Santa Cruz V1 antibody was generated against a human TRPA1 peptide.

    Journal: Journal of Neurochemistry

    Article Title: Validation of TRPA1 and TRPV1 Antibodies for Expression Detection in Mammalian Cells and Tissues

    doi: 10.1111/jnc.70444

    Figure Lengend Snippet: Calcium imaging and immunocytochemistry showing TRPV1 expression in transfected HEK‐293 cells. (A) Fura2 calcium imaging in HEK‐293 cells transiently expressing rTRPV1‐EYFP fusion protein. Representative traces of calcium transients evoked by capsaicin in EYFP + cells. Green traces correspond to EYFP + cells and gray traces to EYFP − cells. Pie chart represents the percentage of EYFP + cells that responded or failded to respond to capsaicin. Data obtained from 88 cells from 3 coverslips. (B–F left) Confocal images of TRPV1‐EYFP transiently expressed in HEK‐293 cells. EYFP (green), TRPV1 antibody (magenta) and Hoechst (HO, blue). Merge images correspond to the overlap between TRPV1 and EYFP on the left and Hoechst and brightfield (BF) on the right. Antibody dilution of the representative images is indicated in the lower right corner. Scale bar: 20 μm. (B–F right) Box plots display the specificity ratio (SR) for each tested dilution of the corresponding antibody. Each dot represents a single EYFP + cell. Boxes indicate the interquartile range (25th to 75th percentiles) and whiskers extend to the 5th and 95th percentiles. The horizontal line inside each box marks the median and the black dot indicates the mean. (*** p < 0.001 Mann–Whitney test). (G) Bar histogram graph summarizes the SR median difference between the tested antibody dilution and their controls lacking primary antibody (secondary antibody only; rabbit, goat or guinea pig) as calculated with the Hodges‐Lehman estimator. Error bars represent the 95% confidence interval. For each antibody and dilution, a minimum of 100 cells were analyzed across 4 fields from 2 independent transfections. $ Santa Cruz V1 antibody was generated against a human TRPA1 peptide.

    Article Snippet: Novus , TRPA1 , Rabbit , Novus Biologicals (Biotechne) , Human TRPA1 N‐terminus (1–100) PC , 77% , NB110‐40763 RRID:AB_715124.

    Techniques: Imaging, Immunocytochemistry, Expressing, Transfection, MANN-WHITNEY, Generated

    Calcium imaging and immunocytochemistry of TRPA1 expression in transfected HEK‐ 293 cells. (A) Representative traces of Fura2 calcium transients evoked by 50 μM AITC. Green traces correspond to tGFP + cells and gray traces to tGFP − cells. The pie chart represents the proportion of tGFP + cells that responded or failed to respond to AITC. Data obtained from 115 cells from 3 coverslips. (B–H left) Confocal images of TRPA1‐tGFP transiently expressed in HEK‐ 293 cells incubated with the indicated antibody. tGFP (green), TRPA1 (magenta) and Hoechst staining (blue). Merge images correspond to the overlap between TRPA1 and tGFP (lower‐left panel) or Hoechst and brightfield (HO, BF, lower‐right). Antibody dilution of the representative images is indicated in the lower right‐hand corner. Scale bar: 20 μm. (B–H right) box plots display the specificity ratio (SR) for each tested dilution of the corresponding antibody. Each dot represents a single tGFP + cell. Boxes indicate the interquartile range (25th to 75th percentiles) and whiskers extend to the 5th and 95th percentiles. The horizontal line inside each box marks the median and the black dot indicates the mean. (** p < 0.01, *** p < 0.001 Mann–Whitney test). (I) Bar histogram graph summarizes the SR median difference between the tested antibody dilution and their controls lacking primary antibody (secondary antibody only; rabbit or mouse) as calculated with the Hodges‐Lehman estimator. Error bars represent the 95% confidence interval. For each antibody and dilution, a minimum of 319 cells were analyzed across 4 fields from 2 independent transfections.

    Journal: Journal of Neurochemistry

    Article Title: Validation of TRPA1 and TRPV1 Antibodies for Expression Detection in Mammalian Cells and Tissues

    doi: 10.1111/jnc.70444

    Figure Lengend Snippet: Calcium imaging and immunocytochemistry of TRPA1 expression in transfected HEK‐ 293 cells. (A) Representative traces of Fura2 calcium transients evoked by 50 μM AITC. Green traces correspond to tGFP + cells and gray traces to tGFP − cells. The pie chart represents the proportion of tGFP + cells that responded or failed to respond to AITC. Data obtained from 115 cells from 3 coverslips. (B–H left) Confocal images of TRPA1‐tGFP transiently expressed in HEK‐ 293 cells incubated with the indicated antibody. tGFP (green), TRPA1 (magenta) and Hoechst staining (blue). Merge images correspond to the overlap between TRPA1 and tGFP (lower‐left panel) or Hoechst and brightfield (HO, BF, lower‐right). Antibody dilution of the representative images is indicated in the lower right‐hand corner. Scale bar: 20 μm. (B–H right) box plots display the specificity ratio (SR) for each tested dilution of the corresponding antibody. Each dot represents a single tGFP + cell. Boxes indicate the interquartile range (25th to 75th percentiles) and whiskers extend to the 5th and 95th percentiles. The horizontal line inside each box marks the median and the black dot indicates the mean. (** p < 0.01, *** p < 0.001 Mann–Whitney test). (I) Bar histogram graph summarizes the SR median difference between the tested antibody dilution and their controls lacking primary antibody (secondary antibody only; rabbit or mouse) as calculated with the Hodges‐Lehman estimator. Error bars represent the 95% confidence interval. For each antibody and dilution, a minimum of 319 cells were analyzed across 4 fields from 2 independent transfections.

    Article Snippet: Novus , TRPA1 , Rabbit , Novus Biologicals (Biotechne) , Human TRPA1 N‐terminus (1–100) PC , 77% , NB110‐40763 RRID:AB_715124.

    Techniques: Imaging, Immunocytochemistry, Expressing, Transfection, Incubation, Staining, MANN-WHITNEY

    Western blot analysis for TRPV1 and TRPA1 antibodies specificity. (A) Immunoblots for TRPV1 using Abcam (1:1000), Millipore V1 (1:1000), Santa Cruz V1 (1:100), Neuromics GT (1:200), and Neuromics GP (1:1000) antibodies. (−) lanes: Untransfected HEK‐293 cells, (+) lanes: HEK‐293 cells transfected with rTRPV1‐EYFP (B) Immunoblots for TRPA1 using Aviva (1:300), Novus (1:500), Millipore A1 (1:500), Alomone (1:200), Proteintech (1:500), Sigma WH (1:500), and Santa Cruz A1 (1:100). (−) lanes: Untransfected HEK‐293 cells, (+) lanes: HEK‐293 cells transfected with hTRPA1‐tGFFP. For each antibody, top row: Immunoblot with each TRPV1/TRPA1 antibody. Middle row: EYFP/tGFP immunoblotting of the same membrane. Bottom image: GAPDH loading control. Each blot was performed at least three times to rule out technical artifacts in cases where no anti‐TRPV1/TRPA1 signal was detected. For every repetition, the identical lysate sample was probed with all antibodies. Full uncropped blots are available in the Figure . $ Santa Cruz V1 antibody was generated against a human TRPA1 peptide.

    Journal: Journal of Neurochemistry

    Article Title: Validation of TRPA1 and TRPV1 Antibodies for Expression Detection in Mammalian Cells and Tissues

    doi: 10.1111/jnc.70444

    Figure Lengend Snippet: Western blot analysis for TRPV1 and TRPA1 antibodies specificity. (A) Immunoblots for TRPV1 using Abcam (1:1000), Millipore V1 (1:1000), Santa Cruz V1 (1:100), Neuromics GT (1:200), and Neuromics GP (1:1000) antibodies. (−) lanes: Untransfected HEK‐293 cells, (+) lanes: HEK‐293 cells transfected with rTRPV1‐EYFP (B) Immunoblots for TRPA1 using Aviva (1:300), Novus (1:500), Millipore A1 (1:500), Alomone (1:200), Proteintech (1:500), Sigma WH (1:500), and Santa Cruz A1 (1:100). (−) lanes: Untransfected HEK‐293 cells, (+) lanes: HEK‐293 cells transfected with hTRPA1‐tGFFP. For each antibody, top row: Immunoblot with each TRPV1/TRPA1 antibody. Middle row: EYFP/tGFP immunoblotting of the same membrane. Bottom image: GAPDH loading control. Each blot was performed at least three times to rule out technical artifacts in cases where no anti‐TRPV1/TRPA1 signal was detected. For every repetition, the identical lysate sample was probed with all antibodies. Full uncropped blots are available in the Figure . $ Santa Cruz V1 antibody was generated against a human TRPA1 peptide.

    Article Snippet: Novus , TRPA1 , Rabbit , Novus Biologicals (Biotechne) , Human TRPA1 N‐terminus (1–100) PC , 77% , NB110‐40763 RRID:AB_715124.

    Techniques: Western Blot, Transfection, Membrane, Control, Generated

    Calcium imaging and Immunochemistry of endogenous TRPA1 in cultured DRG neurons from TRPA1‐Cre‐ChR2‐EYFP mice. (A) Representative traces of calcium transients evoked by AITC and capsaicin in DRG neurons. Traces corresponding to cells responding to 50 μM AITC are displayed in yellow and non‐responding cells are displayed in gray. (B) The pie chart represents the proportion of neurons responding or failing to respond to AITC. Data obtained from 424 cells from 5 coverslips. (C–F) ICC or (G–J) IHC confocal images of DRG sensory neurons incubated with the indicated antibody. TRPA1 antibody (magenta) and βIIITubulin (cyan), merge images display TRPA1 antibody signal + βIII‐Tubulin. Dilution of the corresponding antibody shown in each example is indicated in the lower right corner. Scale bar: 50 μm. Representative images were chosen from 4 pictures of 2 different animals.

    Journal: Journal of Neurochemistry

    Article Title: Validation of TRPA1 and TRPV1 Antibodies for Expression Detection in Mammalian Cells and Tissues

    doi: 10.1111/jnc.70444

    Figure Lengend Snippet: Calcium imaging and Immunochemistry of endogenous TRPA1 in cultured DRG neurons from TRPA1‐Cre‐ChR2‐EYFP mice. (A) Representative traces of calcium transients evoked by AITC and capsaicin in DRG neurons. Traces corresponding to cells responding to 50 μM AITC are displayed in yellow and non‐responding cells are displayed in gray. (B) The pie chart represents the proportion of neurons responding or failing to respond to AITC. Data obtained from 424 cells from 5 coverslips. (C–F) ICC or (G–J) IHC confocal images of DRG sensory neurons incubated with the indicated antibody. TRPA1 antibody (magenta) and βIIITubulin (cyan), merge images display TRPA1 antibody signal + βIII‐Tubulin. Dilution of the corresponding antibody shown in each example is indicated in the lower right corner. Scale bar: 50 μm. Representative images were chosen from 4 pictures of 2 different animals.

    Article Snippet: Novus , TRPA1 , Rabbit , Novus Biologicals (Biotechne) , Human TRPA1 N‐terminus (1–100) PC , 77% , NB110‐40763 RRID:AB_715124.

    Techniques: Imaging, Cell Culture, Incubation

    mtSTAT3 regulates mitochondrial function and fibrosis in human intestinal cells. Overexpression of mtSTAT3 reduced the fibrosis marker C18. (A) Lysates of C18 cells transfected with mock and mtSTAT3 overexpression vector were analyzed for mtSTAT3 protein in mitochondria by Western blotting. (B, C) mRNA levels of the OXPHOS complex genes COX4 and ATP5O and the fibrosis genes aSMA, fibronectin, and COL1A1 according to real-time PCR.

    Journal: Frontiers in Immunology

    Article Title: Overexpression of mitochondrial STAT3 protein improves colonic inflammation and fibrosis in inflammatory bowel disease by enhancing mitochondrial function

    doi: 10.3389/fimmu.2026.1728341

    Figure Lengend Snippet: mtSTAT3 regulates mitochondrial function and fibrosis in human intestinal cells. Overexpression of mtSTAT3 reduced the fibrosis marker C18. (A) Lysates of C18 cells transfected with mock and mtSTAT3 overexpression vector were analyzed for mtSTAT3 protein in mitochondria by Western blotting. (B, C) mRNA levels of the OXPHOS complex genes COX4 and ATP5O and the fibrosis genes aSMA, fibronectin, and COL1A1 according to real-time PCR.

    Article Snippet: The tissue sections were stained for COX4 (NB110–39115; Novus, St. Louis, MO, USA), p727-STAT3 (ab32143; Abcam, Cambridge, UK), and DAPI (D3571; Invitrogen, Waltham, MA, USA); washed with phosphate-buffered saline (PBS); fixed in 4% paraformaldehyde; washed again with PBS; and blocked for 30 min with 10% normal goat serum.

    Techniques: Over Expression, Marker, Transfection, Plasmid Preparation, Western Blot, Real-time Polymerase Chain Reaction