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anti gsdmd antibody  (Proteintech)


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    Structured Review

    Proteintech anti gsdmd antibody
    <t>GSDMD</t> is upregulated <t>in</t> <t>intestinal</t> cancer. ( A ) IHC analysis of GSDMD protein level in a human tissue microarray, including 80 colorectal cancer and matched adjacent tumor specimens. ( B ) IHC analysis of GSDMD protein level in four colorectal cancer tissue and matched adjacent cancer tissue from ( A ) (200× magnification). ( C - E ) GSDMD expression score in cytoplasm ( C ), nuclear ( D ), and cytoplasm + nuclear ( E ) as calculated by multiplying the intensity and positive percentage scores according to ( A ). ( F ) Western blot analysis of GSDMD in in small intestine tumor tissue from Apc min/+ mice ( n = 5) and normal tissue from WT mice ( n = 3). Data are representative of at least three independent experiments (mean ± SEM). *** p < 0.001 by Student’s t test. FL means full length
    Anti Gsdmd Antibody, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 584 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/immunohistochemistry+microarray+based+expression+data/GSDMD+Antibody/pmc11492562-54-0-2
    Average 96 stars, based on 584 article reviews
    anti gsdmd antibody - by Bioz Stars, 2026-10
    96/100 stars

    Images

    1) Product Images from "Gasdermin D promotes development of intestinal tumors through regulating IL-1β release and gut microbiota composition"

    Article Title: Gasdermin D promotes development of intestinal tumors through regulating IL-1β release and gut microbiota composition

    Journal: Cell Communication and Signaling : CCS

    doi: 10.1186/s12964-024-01890-6

    GSDMD is upregulated in intestinal cancer. ( A ) IHC analysis of GSDMD protein level in a human tissue microarray, including 80 colorectal cancer and matched adjacent tumor specimens. ( B ) IHC analysis of GSDMD protein level in four colorectal cancer tissue and matched adjacent cancer tissue from ( A ) (200× magnification). ( C - E ) GSDMD expression score in cytoplasm ( C ), nuclear ( D ), and cytoplasm + nuclear ( E ) as calculated by multiplying the intensity and positive percentage scores according to ( A ). ( F ) Western blot analysis of GSDMD in in small intestine tumor tissue from Apc min/+ mice ( n = 5) and normal tissue from WT mice ( n = 3). Data are representative of at least three independent experiments (mean ± SEM). *** p < 0.001 by Student’s t test. FL means full length
    Figure Legend Snippet: GSDMD is upregulated in intestinal cancer. ( A ) IHC analysis of GSDMD protein level in a human tissue microarray, including 80 colorectal cancer and matched adjacent tumor specimens. ( B ) IHC analysis of GSDMD protein level in four colorectal cancer tissue and matched adjacent cancer tissue from ( A ) (200× magnification). ( C - E ) GSDMD expression score in cytoplasm ( C ), nuclear ( D ), and cytoplasm + nuclear ( E ) as calculated by multiplying the intensity and positive percentage scores according to ( A ). ( F ) Western blot analysis of GSDMD in in small intestine tumor tissue from Apc min/+ mice ( n = 5) and normal tissue from WT mice ( n = 3). Data are representative of at least three independent experiments (mean ± SEM). *** p < 0.001 by Student’s t test. FL means full length

    Techniques Used: Microarray, Expressing, Western Blot

    Deficiency of GSDMD suppresses spontaneous intestinal cancer development. ( A ) Macroscopic view of representative small intestine from 20-week old Apc min/+ and Apc min/+ Gsdmd −/− mice. ( B ) Hematoxylin and eosin (H&E) staining of the representative intestinal tumor from the Apc min/+ and Apc min/+ Gsdmd −/− mice as in ( A ) (100× magnification). ( C - F ) Tumor number ( C and E ) and tumor load ( D and F ) from the small intestines or colons of 20-week-old Apc min/+ ( n = 7) and Apc min/+ Gsdmd −/− ( n = 7) mice. ( G ) Histogram showing the size distribution of tumors from the small intestines of 20-week-old Apc min/+ ( n = 7) and Apc min/+ Gsdmd −/− ( n = 7) mice. ( H - J ) Hematocrit ( H ), thymus weight ( I ) and spleen weight ( J ) of 20-week-old Apc min/+ ( n = 6–7) and Apc min/+ Gsdmd −/− ( n = 6–7) mice. Data are representative of at least three independent experiments (mean ± SEM). * p < 0.05, ** p < 0.01, *** p < 0.001 by Student’s t test
    Figure Legend Snippet: Deficiency of GSDMD suppresses spontaneous intestinal cancer development. ( A ) Macroscopic view of representative small intestine from 20-week old Apc min/+ and Apc min/+ Gsdmd −/− mice. ( B ) Hematoxylin and eosin (H&E) staining of the representative intestinal tumor from the Apc min/+ and Apc min/+ Gsdmd −/− mice as in ( A ) (100× magnification). ( C - F ) Tumor number ( C and E ) and tumor load ( D and F ) from the small intestines or colons of 20-week-old Apc min/+ ( n = 7) and Apc min/+ Gsdmd −/− ( n = 7) mice. ( G ) Histogram showing the size distribution of tumors from the small intestines of 20-week-old Apc min/+ ( n = 7) and Apc min/+ Gsdmd −/− ( n = 7) mice. ( H - J ) Hematocrit ( H ), thymus weight ( I ) and spleen weight ( J ) of 20-week-old Apc min/+ ( n = 6–7) and Apc min/+ Gsdmd −/− ( n = 6–7) mice. Data are representative of at least three independent experiments (mean ± SEM). * p < 0.05, ** p < 0.01, *** p < 0.001 by Student’s t test

    Techniques Used: Staining

    Exogenous IL-1β promotes intestinal tumor development in Apc min/+ Gsdmd −/− mice. ( A ) 8-week-old Apc min/+ Gsdmd −/− mice simultaneously received injection of IL-1β or PBS twice a week, while age and sex-matched Apc min/+ mice were injected with PBS ( n = 5–6/group). H&E staining of the representative intestinal tumor from the 20-week old above mice (100× magnification). Tumors are circled with dashed lines. ( B - E ) Tumor number ( B and D ) and tumor load ( C and E ) from the small intestines or colons of 20-week-old above mice as in ( A ). ( F - G ) Spleen weight ( F ), and hematocrit ( G ) of 20-week-old above mice as in ( A ). ( H ) Histogram showing the size distribution of tumors from the small intestines of 20-week-old above mice as in ( A ). Data are representative of at least three independent experiments (mean ± SEM). ** p < 0.01 by Student’s t test. N.S. means no significance
    Figure Legend Snippet: Exogenous IL-1β promotes intestinal tumor development in Apc min/+ Gsdmd −/− mice. ( A ) 8-week-old Apc min/+ Gsdmd −/− mice simultaneously received injection of IL-1β or PBS twice a week, while age and sex-matched Apc min/+ mice were injected with PBS ( n = 5–6/group). H&E staining of the representative intestinal tumor from the 20-week old above mice (100× magnification). Tumors are circled with dashed lines. ( B - E ) Tumor number ( B and D ) and tumor load ( C and E ) from the small intestines or colons of 20-week-old above mice as in ( A ). ( F - G ) Spleen weight ( F ), and hematocrit ( G ) of 20-week-old above mice as in ( A ). ( H ) Histogram showing the size distribution of tumors from the small intestines of 20-week-old above mice as in ( A ). Data are representative of at least three independent experiments (mean ± SEM). ** p < 0.01 by Student’s t test. N.S. means no significance

    Techniques Used: Injection, Staining

    Exogenous Kyn promotes intestinal tumor development in Apc min/+ Gsdmd −/− mice. ( A ) ELISA analysis of Kyn and Trp from colon of Apc min/+ ( n = 6) and Apc min/+ Gsdmd −/− ( n = 6) mice. ( B ) Kyn/Trp was determined as in ( A ). ( C ) 8-week-old Apc min/+ Gsdmd −/− mice simultaneously received injection of Kyn or PBS once a week, while age and sex-matched Apc min/+ mice were injected with PBS ( n = 5/group). H&E staining of the representative intestinal tumor from the 20-week old above mice (100× magnification). ( D - G ) Tumor number ( D and F ) and tumor load ( E and G ) from the small intestines or colons of 20-week-old above mice as in ( C ). ( H - I ) Spleen weight ( H ), and hematocrit ( I ) of 20-week-old above mice as in ( C ). ( J ) Histogram showing the size distribution of tumors from the small intestines of 20-week-old above mice as in ( C ). Data are representative of at least three independent experiments (mean ± SEM). * p < 0.05, ** p < 0.01, *** p < 0.001 by Student’s t test. N.S. means no significance
    Figure Legend Snippet: Exogenous Kyn promotes intestinal tumor development in Apc min/+ Gsdmd −/− mice. ( A ) ELISA analysis of Kyn and Trp from colon of Apc min/+ ( n = 6) and Apc min/+ Gsdmd −/− ( n = 6) mice. ( B ) Kyn/Trp was determined as in ( A ). ( C ) 8-week-old Apc min/+ Gsdmd −/− mice simultaneously received injection of Kyn or PBS once a week, while age and sex-matched Apc min/+ mice were injected with PBS ( n = 5/group). H&E staining of the representative intestinal tumor from the 20-week old above mice (100× magnification). ( D - G ) Tumor number ( D and F ) and tumor load ( E and G ) from the small intestines or colons of 20-week-old above mice as in ( C ). ( H - I ) Spleen weight ( H ), and hematocrit ( I ) of 20-week-old above mice as in ( C ). ( J ) Histogram showing the size distribution of tumors from the small intestines of 20-week-old above mice as in ( C ). Data are representative of at least three independent experiments (mean ± SEM). * p < 0.05, ** p < 0.01, *** p < 0.001 by Student’s t test. N.S. means no significance

    Techniques Used: Enzyme-linked Immunosorbent Assay, Injection, Staining

    Exogenous Kyn increases Treg cell number in Apc min/+ Gsdmd −/− mice. ( A ) 8-week-old Apc min/+ Gsdmd −/− mice simultaneously received injection of Kyn or PBS once a week, while age and sex-matched Apc min/+ mice were injected with PBS ( n = 4/group). Flow cytometry analysis of CD4 + and CD8 + T cell number from intestinal tumor of the 20-week old above mice. ( B ) Total leukocytes were determined by CD45 + cell. CD4 + T cells % of total leukocyte and CD8 + T cells % of total leukocyte were determined as in ( A ). ( C ) Flow cytometry analysis of Treg (CD4 + Foxp3 + ) cell number from intestinal tumor of the 20-week old mice as in ( A ). ( D ) Treg % of CD4 + cells was determined as in ( C ). Data are representative of at least three independent experiments (mean ± SEM). ** p < 0.01, *** p < 0.001 by Student’s t test. N.S. means no significance
    Figure Legend Snippet: Exogenous Kyn increases Treg cell number in Apc min/+ Gsdmd −/− mice. ( A ) 8-week-old Apc min/+ Gsdmd −/− mice simultaneously received injection of Kyn or PBS once a week, while age and sex-matched Apc min/+ mice were injected with PBS ( n = 4/group). Flow cytometry analysis of CD4 + and CD8 + T cell number from intestinal tumor of the 20-week old above mice. ( B ) Total leukocytes were determined by CD45 + cell. CD4 + T cells % of total leukocyte and CD8 + T cells % of total leukocyte were determined as in ( A ). ( C ) Flow cytometry analysis of Treg (CD4 + Foxp3 + ) cell number from intestinal tumor of the 20-week old mice as in ( A ). ( D ) Treg % of CD4 + cells was determined as in ( C ). Data are representative of at least three independent experiments (mean ± SEM). ** p < 0.01, *** p < 0.001 by Student’s t test. N.S. means no significance

    Techniques Used: Injection, Flow Cytometry

    Related Articles

    Incubation:

    Article Title: ADSC-Conditioned Medium Mitigates LPS-Induced Acute Lung Injury by Inhibiting Alveolar Macrophage Pyroptosis.
    Article Snippet: Following fixation with 4% paraformaldehyde, permeabilization with Triton X-100 (Yeasen, Shanghai, China), and washing with PBS, the cells were blocked with 5% BSA for 1 h at room temperature. .. Subsequently, the cells were incubated overnight at 4 ◦C with a combination of primary antibodies targeting GSDMD (1:100, Proteintech, 20770-1-AP, Wuhan, China) and NLRP3 (1:100, Proteintech, 68102-1-Ig). ..

    Article Title: Statins targeting mevalonate-geranylgeranyl diphosphate pathway inhibit proliferation in NK/T lymphoma by promoting pyroptosis.
    Article Snippet: After electrophoretic separation via sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE), the proteins were electroblotted onto nitrocellulose membranes (66485, PALL, USA) using a semi-dry transfer system. .. The membranes were then incubated with primary antibodies against pro-caspase-1 (1:1000, ab179515, Abcam, England), cleaved caspase-1 (1:1000, 4199, CST, USA), GSDMD (1:2000, 20770-1-AP, Proteintech, Wuhan, China), cleaved N-terminal GSDMD (1:1000, ab215203, Abcam), IL-18 (1:5000, 10663-1-AP, Proteintech), IL-1β (1:1,000, 26048-1-AP, Proteintech), GSDME (1:2000, 13075-1-AP, Proteintech) and β-actin (1:5000, 66009-1-lg, Proteintech) overnight at 4 ◦C. .. Then the membranes were cultured with secondary antibodies (1:5000, SA00001-1 and SA00001-2, Proteintech) for 1 hour at room temperature.

    Article Title: Pharmacological Targeting of CXCR4 Attenuates Sepsis-Induced Intestinal Injury by Suppressing NLRP3/GSDMD-Mediated Pyroptosis.
    Article Snippet: .. After blocking with 10% goat serum, sections were incubated overnight at 4°C with primary antibodies against: Anti-GSDMD (1:200, Proteintech, #20770-1-AP) and Anti-Cytokeratin19 (1:200, Proteintech, #10712-1-AP). .. A species-matched secondary antibody Goat anti-rabbit IgG-Cy3 (1:50, ZSGB-BIO, #ZF-0316) was applied.

    other:

    Article Title: FOXE1 promotes the progression of pulp inflammation by activating PANoptosis in dental pulp cells
    Article Snippet: Anti-pro and cleaved GSDMD , Proteintech , Cat# 20770-1-AP, RRID: AB_10696319.

    Blocking Assay:

    Article Title: Pharmacological Targeting of CXCR4 Attenuates Sepsis-Induced Intestinal Injury by Suppressing NLRP3/GSDMD-Mediated Pyroptosis.
    Article Snippet: .. After blocking with 10% goat serum, sections were incubated overnight at 4°C with primary antibodies against: Anti-GSDMD (1:200, Proteintech, #20770-1-AP) and Anti-Cytokeratin19 (1:200, Proteintech, #10712-1-AP). .. A species-matched secondary antibody Goat anti-rabbit IgG-Cy3 (1:50, ZSGB-BIO, #ZF-0316) was applied.



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