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rabbit anti cd3  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit anti cd3
    Rabbit Anti Cd3, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+cd3+antibody/pm41723466-156-11-14
    Average 86 stars, based on 1 article reviews
    rabbit anti cd3 - by Bioz Stars, 2026-09
    86/100 stars

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    Related Articles

    Expressing:

    Article Title: PCDHGA10 as a potential prognostic biomarker and correlated with immune infiltration in gastric cancer.
    Article Snippet: The pathologists set the threshold of each marker to ensure an accuracy of more than 95%.The pathologists set the threshold of each marker to ensure an accuracy of more than 95%.. This study used the following primary antibodies: rabbit antiPCDHGA10 (1:50, D1247, Biobyt), rabbit anti-CD11b antibody (1:100, 49420S, CST), rabbit anti-CD8 antibody (1:100, ab83278, Frontiers in Immunology 03 Abcam), rabbit anti-CD3 antibody (1:200, 85061S, CST), rabbit anti-CD4 antibody (1:200, ab133616, Abcam), mouse anti-Foxp-3 antibody (1:50, ab20034, Abcam), anti-LAG-3 antibody (1:50, ab52587, Abcam), anti-CD66b antibody (1:500, ab214175, Abcam), anti-cytokeratin antibody (1:8000, orb69073, Biobyt), anti-CD68 antibody (1:500, 797778S, CST).. The secondary antibody was OpalTM polymer HRP Ms+Rb (211011069, Akoya Bioscience).The secondary antibody was OpalTM polymer HRP Ms+Rb (211011069, Akoya Bioscience).

    Article Title: PCDHGA10 as a potential prognostic biomarker and correlated with immune infiltration in gastric cancer
    Article Snippet: The pathologists set the threshold of each marker to ensure an accuracy of more than 95%.The pathologists set the threshold of each marker to ensure an accuracy of more than 95%.. This study used the following primary antibodies: rabbit anti-PCDHGA10 (1:50, D1247, Biobyt), rabbit anti-CD11b antibody (1:100, 49420S, CST), rabbit anti-CD8 antibody (1:100, ab83278, Abcam), rabbit anti-CD3 antibody (1:200, 85061S, CST), rabbit anti-CD4 antibody (1:200, ab133616, Abcam), mouse anti-Foxp-3 antibody (1:50, ab20034, Abcam), anti-LAG-3 antibody (1:50, ab52587, Abcam), anti-CD66b antibody (1:500, ab214175, Abcam), anti-cytokeratin antibody (1:8000, orb69073, Biobyt), anti-CD68 antibody (1:500, 797778S, CST).. The secondary antibody was Opal™ polymer HRP Ms + Rb (211011069, Akoya Bioscience).The secondary antibody was Opal™ polymer HRP Ms + Rb (211011069, Akoya Bioscience).

    Article Title: Marsdenia tenacissima enhances immune response of tumor infiltrating T lymphocytes to colorectal cancer
    Article Snippet: Human XL Cytokine Array Kit (#ARY022B) was purchased from R&D Systems, Inc (Minneapolis, MN, USA).Human XL Cytokine Array Kit (#ARY022B) was purchased from R&D Systems, Inc (Minneapolis, MN, USA).. Rabbit anti-CD3 antibody (#85061), rabbit anti-CD8 antibody (#85336), rabbit anti-PD-1 antibody (#86163) and rabbit anti-PD-L1 antibody (#13684) were purchased from Cell Signaling Technology Co., Ltd (Danvers, MA, US).. Goat anti-rabbit IgG-HRP antibody (#P0615) were purchased from Beyotime Biotech Inc. Rabbit anti-FOXP3 antibody (#PB0043) was purchased from Boster Biological Technology Co., Ltd (Wuhan, Hubei, China).Goat anti-rabbit IgG-HRP antibody (#P0615) were purchased from Beyotime Biotech Inc. Rabbit anti-FOXP3 antibody (#PB0043) was purchased from Boster Biological Technology Co., Ltd (Wuhan, Hubei, China).



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    cd3  (Cell Signaling Technology Inc)
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    Cell Signaling Technology Inc cd3
    ( a ) Western blot to confirm the loss of Ass1 protein expression in YUMM1.7 Ass1 knockout cells (Ass1-KO). β-ACTIN was used as a loading control. ( b ) Ass1-wildtype (Ass1-WT) or Ass1-KO cells were subcutaneously injected into C57BL/6J mice for tumor growth curve. Ass1-KO melanomas does not grow compared to wiltype controls. ( c ) Ass1-WT or Ass1-KO melanomas were collected for histology. IHC staining shows more Cd8+ T cells infiltrated into Ass1-KO melanomas compared to wildtype controls. ( d ) YUMM1.7-WT or Ass1-KO cells were subcutaneously injected into NSG or C57BL/6J respectively for tumor growth curve. Ass1-KO melanomas grow in NSG mice, but not in C57BL/6J mice. ( e ) IHC staining of <t>Cd3</t> to detect T cells in tumors collected from d. ( f ) YUMM1.7 wiltype cells were subcutaneously injected into C57BL/6J mice and treated with IgG or anti-PD1. Tumors were measured for growth curve. NS indicates no significance.
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    rabbit anti hcd3 mabs  (fluidigm)
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    ( a ) Western blot to confirm the loss of Ass1 protein expression in YUMM1.7 Ass1 knockout cells (Ass1-KO). β-ACTIN was used as a loading control. ( b ) Ass1-wildtype (Ass1-WT) or Ass1-KO cells were subcutaneously injected into C57BL/6J mice for tumor growth curve. Ass1-KO melanomas does not grow compared to wiltype controls. ( c ) Ass1-WT or Ass1-KO melanomas were collected for histology. IHC staining shows more Cd8+ T cells infiltrated into Ass1-KO melanomas compared to wildtype controls. ( d ) YUMM1.7-WT or Ass1-KO cells were subcutaneously injected into NSG or C57BL/6J respectively for tumor growth curve. Ass1-KO melanomas grow in NSG mice, but not in C57BL/6J mice. ( e ) IHC staining of <t>Cd3</t> to detect T cells in tumors collected from d. ( f ) YUMM1.7 wiltype cells were subcutaneously injected into C57BL/6J mice and treated with IgG or anti-PD1. Tumors were measured for growth curve. NS indicates no significance.
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    Image Search Results


    ( a ) Western blot to confirm the loss of Ass1 protein expression in YUMM1.7 Ass1 knockout cells (Ass1-KO). β-ACTIN was used as a loading control. ( b ) Ass1-wildtype (Ass1-WT) or Ass1-KO cells were subcutaneously injected into C57BL/6J mice for tumor growth curve. Ass1-KO melanomas does not grow compared to wiltype controls. ( c ) Ass1-WT or Ass1-KO melanomas were collected for histology. IHC staining shows more Cd8+ T cells infiltrated into Ass1-KO melanomas compared to wildtype controls. ( d ) YUMM1.7-WT or Ass1-KO cells were subcutaneously injected into NSG or C57BL/6J respectively for tumor growth curve. Ass1-KO melanomas grow in NSG mice, but not in C57BL/6J mice. ( e ) IHC staining of Cd3 to detect T cells in tumors collected from d. ( f ) YUMM1.7 wiltype cells were subcutaneously injected into C57BL/6J mice and treated with IgG or anti-PD1. Tumors were measured for growth curve. NS indicates no significance.

    Journal: bioRxiv

    Article Title: MYC-ATF4-ASS1 axis governs intracellular arginine synthesis and dictates the immune microenvironment in melanoma

    doi: 10.64898/2026.02.27.707779

    Figure Lengend Snippet: ( a ) Western blot to confirm the loss of Ass1 protein expression in YUMM1.7 Ass1 knockout cells (Ass1-KO). β-ACTIN was used as a loading control. ( b ) Ass1-wildtype (Ass1-WT) or Ass1-KO cells were subcutaneously injected into C57BL/6J mice for tumor growth curve. Ass1-KO melanomas does not grow compared to wiltype controls. ( c ) Ass1-WT or Ass1-KO melanomas were collected for histology. IHC staining shows more Cd8+ T cells infiltrated into Ass1-KO melanomas compared to wildtype controls. ( d ) YUMM1.7-WT or Ass1-KO cells were subcutaneously injected into NSG or C57BL/6J respectively for tumor growth curve. Ass1-KO melanomas grow in NSG mice, but not in C57BL/6J mice. ( e ) IHC staining of Cd3 to detect T cells in tumors collected from d. ( f ) YUMM1.7 wiltype cells were subcutaneously injected into C57BL/6J mice and treated with IgG or anti-PD1. Tumors were measured for growth curve. NS indicates no significance.

    Article Snippet: Primary antibodies against Ki67 (Thermo Fisher Scientific, MA5-14520), F4/80 (CST, 70076S), Cd8 (98941S), Cd3 (78588S), Cd20 (70168S) were diluted 1:200 in PBST buffer and incubated with slides overnight at 4°C on a shaker.

    Techniques: Western Blot, Expressing, Knock-Out, Control, Injection, Immunohistochemistry