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sdhc  (Boster Bio)


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    Structured Review

    Boster Bio sdhc
    Sdhc, supplied by Boster Bio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sdhc/product/Boster Bio
    Average 93 stars, based on 1 article reviews
    sdhc - by Bioz Stars, 2026-05
    93/100 stars

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    Proteintech antibody against sdhc
    A) Schematic showing the xenograft tumor model with subcutaneous implantation. B) Tumor weight from B) C) Lipid ROS are measured by C11-BODIPY581/591 in EPCAM positive cells from the tumors from B). D) Schematic showing breeding strategy to generate tamoxifen inducible intestine specific <t>SDHC</t> deficient mice. E) Western blot images showing cellular and mitochondrial protein expression of SDHC 5days post tamoxifen induction via 100mg/kg body weight I.P. injection in WT ( Sdhc +/+), Het ( Sdhc +/-) and KO ( Sdhc -/-) mice. F) Representative H&E images of Sdhc F/F and Sdhc ΔIE mice fed with 350 ppm or 1000ppm iron containing chow for 7 days. G) Inflammatory histology scored for small intestine and colon of Sdhc F/F and Sdhc ΔIE mice fed with 350 ppm or 1000ppm iron containing chow for 7 days. H) Representative immunohistochemistry images showing accumulation of 4 <t>hydroxynonenal</t> <t>(4HNE)</t> in small intestine and colon of Sdhc F/F and Sdhc ΔIE mice fed with 350 ppm or 1000ppm iron containing chow for 7 days. I) Schematic showing treatment protocol for colitis associated cancer model using AOM/DSS in Sdhc F/F (WT) and Sdhc Het IE (Het) mice. J) Tumor number measured in mice from I). K) Tumor burden measured in mice from I) L) Lipid ROS measured by C11-BODIPY581/591 in EPCAM positive epithelial cells derived from I). M) Schematic showing role of heme-SDHC-CoQ axis in mitigating iron induced cell death in CRC cells. All data are mean ± SEM. One-way ANOVA with Tukey’s multiple comparisons test for (B) and (G) and t test for (C), (J), (K) and (L). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001.
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    A) Western blot images showing protein expression <t>of</t> <t>SDHA,</t> SDHB and beta actin in SDHA and SDHB knockdown HT29 cells via constitutive shRNA expression. B) Representative crystal violet staining of HT29 SDHA and <t>SDHC</t> knockdown cells from A) 14 days post copper sulphate (100μM) + elesclomol (Cu-Es), C) hydrogen peroxide (H 2 O 2 ) and D) 5-fluoroUracil (5FU) at indicated concentrations. E) Heatmap representation of relative colony count from B). F) Representative crystal violet staining images 14 days post FAC (at indicated concentrations), dimethyl succinate, dimethyl malonate, and diethyl malonate. G) Representative crystal violet staining image of NDUSF1 and 2 knockdown cells 14 days post FAC treatment (0.25, 0.5mM) with or without SA (250μM) or heme (10μM).
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    A) Western blot images showing protein expression <t>of</t> <t>SDHA,</t> SDHB and beta actin in SDHA and SDHB knockdown HT29 cells via constitutive shRNA expression. B) Representative crystal violet staining of HT29 SDHA and <t>SDHC</t> knockdown cells from A) 14 days post copper sulphate (100μM) + elesclomol (Cu-Es), C) hydrogen peroxide (H 2 O 2 ) and D) 5-fluoroUracil (5FU) at indicated concentrations. E) Heatmap representation of relative colony count from B). F) Representative crystal violet staining images 14 days post FAC (at indicated concentrations), dimethyl succinate, dimethyl malonate, and diethyl malonate. G) Representative crystal violet staining image of NDUSF1 and 2 knockdown cells 14 days post FAC treatment (0.25, 0.5mM) with or without SA (250μM) or heme (10μM).
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    Proteintech anti sdhc
    A) Western blot images showing protein expression <t>of</t> <t>SDHA,</t> SDHB and beta actin in SDHA and SDHB knockdown HT29 cells via constitutive shRNA expression. B) Representative crystal violet staining of HT29 SDHA and <t>SDHC</t> knockdown cells from A) 14 days post copper sulphate (100μM) + elesclomol (Cu-Es), C) hydrogen peroxide (H 2 O 2 ) and D) 5-fluoroUracil (5FU) at indicated concentrations. E) Heatmap representation of relative colony count from B). F) Representative crystal violet staining images 14 days post FAC (at indicated concentrations), dimethyl succinate, dimethyl malonate, and diethyl malonate. G) Representative crystal violet staining image of NDUSF1 and 2 knockdown cells 14 days post FAC treatment (0.25, 0.5mM) with or without SA (250μM) or heme (10μM).
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    Thermo Fisher gene exp sdhc hs01698067 s1
    H2/Z14 and C6/Z96 modulate SDH subunit protein abundance.( a ) Normalized expression of SDHA , SDHB , <t>SDHC</t> , and SDHD across human lung adenocarcinoma (LUAD, N=80) and immortalized lung epithelial & fibroblast cell lines (Lung, N=8) from the Human Protein Atlas database. Expression levels are presented as normalized transcript per million (nTPM), b,c Immunofluorescent staining ( b ) and quantification ( c ) of SDHA and SDHD in H1975 cells treated with or without H2/Z14 and C6/Z96 (30 µM) for six hours. Cells were co-stained with primary anti-SDHA and anti-SDHD antibodies, followed by secondary antibodies conjugated with Alexa Fluor 488 or 555. The cells were then counterstained with DAPI and imaged by confocal microscopy. Scale bar = 20 µm. N = 6 replicates. ( d ) Western blot analysis of SDHA in H1975 cells treated with or without H2/Z14 and C6/Z96 (30 µM) for four hours. Band intensity was quantified and is shown below the images. β-Actin was used as a loading control. The images were representative of data from two independent experiments. Data are mean ± s.e.m. and were analyzed with Welch’s t-test ( a , c ). **, p <0.01; ***, p <0.001; ns, not significant
    Gene Exp Sdhc Hs01698067 S1, supplied by Thermo Fisher, 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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    H2/Z14 and C6/Z96 modulate SDH subunit protein abundance.( a ) Normalized expression of SDHA , SDHB , <t>SDHC</t> , and SDHD across human lung adenocarcinoma (LUAD, N=80) and immortalized lung epithelial & fibroblast cell lines (Lung, N=8) from the Human Protein Atlas database. Expression levels are presented as normalized transcript per million (nTPM), b,c Immunofluorescent staining ( b ) and quantification ( c ) of SDHA and SDHD in H1975 cells treated with or without H2/Z14 and C6/Z96 (30 µM) for six hours. Cells were co-stained with primary anti-SDHA and anti-SDHD antibodies, followed by secondary antibodies conjugated with Alexa Fluor 488 or 555. The cells were then counterstained with DAPI and imaged by confocal microscopy. Scale bar = 20 µm. N = 6 replicates. ( d ) Western blot analysis of SDHA in H1975 cells treated with or without H2/Z14 and C6/Z96 (30 µM) for four hours. Band intensity was quantified and is shown below the images. β-Actin was used as a loading control. The images were representative of data from two independent experiments. Data are mean ± s.e.m. and were analyzed with Welch’s t-test ( a , c ). **, p <0.01; ***, p <0.001; ns, not significant
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    Thermo Fisher gene exp sdhc mm00481172 m1
    H2/Z14 and C6/Z96 modulate SDH subunit protein abundance.( a ) Normalized expression of SDHA , SDHB , <t>SDHC</t> , and SDHD across human lung adenocarcinoma (LUAD, N=80) and immortalized lung epithelial & fibroblast cell lines (Lung, N=8) from the Human Protein Atlas database. Expression levels are presented as normalized transcript per million (nTPM), b,c Immunofluorescent staining ( b ) and quantification ( c ) of SDHA and SDHD in H1975 cells treated with or without H2/Z14 and C6/Z96 (30 µM) for six hours. Cells were co-stained with primary anti-SDHA and anti-SDHD antibodies, followed by secondary antibodies conjugated with Alexa Fluor 488 or 555. The cells were then counterstained with DAPI and imaged by confocal microscopy. Scale bar = 20 µm. N = 6 replicates. ( d ) Western blot analysis of SDHA in H1975 cells treated with or without H2/Z14 and C6/Z96 (30 µM) for four hours. Band intensity was quantified and is shown below the images. β-Actin was used as a loading control. The images were representative of data from two independent experiments. Data are mean ± s.e.m. and were analyzed with Welch’s t-test ( a , c ). **, p <0.01; ***, p <0.001; ns, not significant
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    Image Search Results


    A) Schematic showing the xenograft tumor model with subcutaneous implantation. B) Tumor weight from B) C) Lipid ROS are measured by C11-BODIPY581/591 in EPCAM positive cells from the tumors from B). D) Schematic showing breeding strategy to generate tamoxifen inducible intestine specific SDHC deficient mice. E) Western blot images showing cellular and mitochondrial protein expression of SDHC 5days post tamoxifen induction via 100mg/kg body weight I.P. injection in WT ( Sdhc +/+), Het ( Sdhc +/-) and KO ( Sdhc -/-) mice. F) Representative H&E images of Sdhc F/F and Sdhc ΔIE mice fed with 350 ppm or 1000ppm iron containing chow for 7 days. G) Inflammatory histology scored for small intestine and colon of Sdhc F/F and Sdhc ΔIE mice fed with 350 ppm or 1000ppm iron containing chow for 7 days. H) Representative immunohistochemistry images showing accumulation of 4 hydroxynonenal (4HNE) in small intestine and colon of Sdhc F/F and Sdhc ΔIE mice fed with 350 ppm or 1000ppm iron containing chow for 7 days. I) Schematic showing treatment protocol for colitis associated cancer model using AOM/DSS in Sdhc F/F (WT) and Sdhc Het IE (Het) mice. J) Tumor number measured in mice from I). K) Tumor burden measured in mice from I) L) Lipid ROS measured by C11-BODIPY581/591 in EPCAM positive epithelial cells derived from I). M) Schematic showing role of heme-SDHC-CoQ axis in mitigating iron induced cell death in CRC cells. All data are mean ± SEM. One-way ANOVA with Tukey’s multiple comparisons test for (B) and (G) and t test for (C), (J), (K) and (L). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001.

    Journal: bioRxiv

    Article Title: Iron addicted colorectal cancers exploit Heme-Complex II axis to resist oxidative cell death

    doi: 10.1101/2025.11.05.686813

    Figure Lengend Snippet: A) Schematic showing the xenograft tumor model with subcutaneous implantation. B) Tumor weight from B) C) Lipid ROS are measured by C11-BODIPY581/591 in EPCAM positive cells from the tumors from B). D) Schematic showing breeding strategy to generate tamoxifen inducible intestine specific SDHC deficient mice. E) Western blot images showing cellular and mitochondrial protein expression of SDHC 5days post tamoxifen induction via 100mg/kg body weight I.P. injection in WT ( Sdhc +/+), Het ( Sdhc +/-) and KO ( Sdhc -/-) mice. F) Representative H&E images of Sdhc F/F and Sdhc ΔIE mice fed with 350 ppm or 1000ppm iron containing chow for 7 days. G) Inflammatory histology scored for small intestine and colon of Sdhc F/F and Sdhc ΔIE mice fed with 350 ppm or 1000ppm iron containing chow for 7 days. H) Representative immunohistochemistry images showing accumulation of 4 hydroxynonenal (4HNE) in small intestine and colon of Sdhc F/F and Sdhc ΔIE mice fed with 350 ppm or 1000ppm iron containing chow for 7 days. I) Schematic showing treatment protocol for colitis associated cancer model using AOM/DSS in Sdhc F/F (WT) and Sdhc Het IE (Het) mice. J) Tumor number measured in mice from I). K) Tumor burden measured in mice from I) L) Lipid ROS measured by C11-BODIPY581/591 in EPCAM positive epithelial cells derived from I). M) Schematic showing role of heme-SDHC-CoQ axis in mitigating iron induced cell death in CRC cells. All data are mean ± SEM. One-way ANOVA with Tukey’s multiple comparisons test for (B) and (G) and t test for (C), (J), (K) and (L). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001.

    Article Snippet: Followed by blocking with 5% goat serum in PBS and sections were then probed with primary antibody against SDHC (Proteintech, 14575-AP) or 4HNE (R&D Systems, MAB3249-SP) diluted at 1:500 in the blocking solution.

    Techniques: Western Blot, Expressing, Injection, Immunohistochemistry, Derivative Assay

    A) Western blot images showing protein expression of SDHA, SDHB and beta actin in SDHA and SDHB knockdown HT29 cells via constitutive shRNA expression. B) Representative crystal violet staining of HT29 SDHA and SDHC knockdown cells from A) 14 days post copper sulphate (100μM) + elesclomol (Cu-Es), C) hydrogen peroxide (H 2 O 2 ) and D) 5-fluoroUracil (5FU) at indicated concentrations. E) Heatmap representation of relative colony count from B). F) Representative crystal violet staining images 14 days post FAC (at indicated concentrations), dimethyl succinate, dimethyl malonate, and diethyl malonate. G) Representative crystal violet staining image of NDUSF1 and 2 knockdown cells 14 days post FAC treatment (0.25, 0.5mM) with or without SA (250μM) or heme (10μM).

    Journal: bioRxiv

    Article Title: Iron addicted colorectal cancers exploit Heme-Complex II axis to resist oxidative cell death

    doi: 10.1101/2025.11.05.686813

    Figure Lengend Snippet: A) Western blot images showing protein expression of SDHA, SDHB and beta actin in SDHA and SDHB knockdown HT29 cells via constitutive shRNA expression. B) Representative crystal violet staining of HT29 SDHA and SDHC knockdown cells from A) 14 days post copper sulphate (100μM) + elesclomol (Cu-Es), C) hydrogen peroxide (H 2 O 2 ) and D) 5-fluoroUracil (5FU) at indicated concentrations. E) Heatmap representation of relative colony count from B). F) Representative crystal violet staining images 14 days post FAC (at indicated concentrations), dimethyl succinate, dimethyl malonate, and diethyl malonate. G) Representative crystal violet staining image of NDUSF1 and 2 knockdown cells 14 days post FAC treatment (0.25, 0.5mM) with or without SA (250μM) or heme (10μM).

    Article Snippet: After lysis solubilized proteins were resolved on 12% SDS-polyacrylamide gels and transferred to PVDF membrane, blocked with 5% milk in TBST and probed overnight with indicated primary antibodies diluted at 1:1000 in the blocking buffer for GPX4 (Proteintech, 67763-1-Ig), FTH1 (Cell Signaling,3998S), UROD (Santa Cruz, SC-365297), FECH (Proteintech, 14466-1-AP), SDHA (Cell Signaling, 11998), SDHB (Proteintech, 10620-1-AP), SDHC (Proteintech, 14575-AP), β-actin (Proteintech 66009-1-Ig).

    Techniques: Western Blot, Expressing, Knockdown, shRNA, Staining

    H2/Z14 and C6/Z96 modulate SDH subunit protein abundance.( a ) Normalized expression of SDHA , SDHB , SDHC , and SDHD across human lung adenocarcinoma (LUAD, N=80) and immortalized lung epithelial & fibroblast cell lines (Lung, N=8) from the Human Protein Atlas database. Expression levels are presented as normalized transcript per million (nTPM), b,c Immunofluorescent staining ( b ) and quantification ( c ) of SDHA and SDHD in H1975 cells treated with or without H2/Z14 and C6/Z96 (30 µM) for six hours. Cells were co-stained with primary anti-SDHA and anti-SDHD antibodies, followed by secondary antibodies conjugated with Alexa Fluor 488 or 555. The cells were then counterstained with DAPI and imaged by confocal microscopy. Scale bar = 20 µm. N = 6 replicates. ( d ) Western blot analysis of SDHA in H1975 cells treated with or without H2/Z14 and C6/Z96 (30 µM) for four hours. Band intensity was quantified and is shown below the images. β-Actin was used as a loading control. The images were representative of data from two independent experiments. Data are mean ± s.e.m. and were analyzed with Welch’s t-test ( a , c ). **, p <0.01; ***, p <0.001; ns, not significant

    Journal: Cancer Cell International

    Article Title: Efficient identification of new small molecules targeting succinate dehydrogenase in non-small cell lung cancer

    doi: 10.1186/s12935-025-04002-7

    Figure Lengend Snippet: H2/Z14 and C6/Z96 modulate SDH subunit protein abundance.( a ) Normalized expression of SDHA , SDHB , SDHC , and SDHD across human lung adenocarcinoma (LUAD, N=80) and immortalized lung epithelial & fibroblast cell lines (Lung, N=8) from the Human Protein Atlas database. Expression levels are presented as normalized transcript per million (nTPM), b,c Immunofluorescent staining ( b ) and quantification ( c ) of SDHA and SDHD in H1975 cells treated with or without H2/Z14 and C6/Z96 (30 µM) for six hours. Cells were co-stained with primary anti-SDHA and anti-SDHD antibodies, followed by secondary antibodies conjugated with Alexa Fluor 488 or 555. The cells were then counterstained with DAPI and imaged by confocal microscopy. Scale bar = 20 µm. N = 6 replicates. ( d ) Western blot analysis of SDHA in H1975 cells treated with or without H2/Z14 and C6/Z96 (30 µM) for four hours. Band intensity was quantified and is shown below the images. β-Actin was used as a loading control. The images were representative of data from two independent experiments. Data are mean ± s.e.m. and were analyzed with Welch’s t-test ( a , c ). **, p <0.01; ***, p <0.001; ns, not significant

    Article Snippet: TaqMan probes (Applied Biosystem) included the following: SDHA -Hs00188166_m1 (Cat#4331182), SDHB -Hs00268117_m1 (Cat#4331182), SDHC -Hs01698067_s1 (Cat#4331182), SDHD -Hs00829723_g1 (Cat#4331182), CASP9 -Hs00962278_m1 (Cat#4453320), CYCS -Hs01588974_g1 (Cat#4453320), and GAPDH-Hs02786624_g1 (Cat#4331182).

    Techniques: Quantitative Proteomics, Expressing, Staining, Confocal Microscopy, Western Blot, Control