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isotype control antibody, mouse igg2a  (Miltenyi Biotec)


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    Miltenyi Biotec isotype control antibody, mouse igg2a
    Isotype Control Antibody, Mouse Igg2a, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 74 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/igg2a/Isotype+Control+Antibody%2C+mouse+IgG2a/custom%40130-113-833%4042727576
    Average 95 stars, based on 74 article reviews
    isotype control antibody, mouse igg2a - by Bioz Stars, 2026-09
    95/100 stars

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    Article Title: Leukemia Inhibitory Factor Is Required for Subventricular Zone Astrocyte Progenitor Proliferation and for Prokineticin-2 Production after a Closed Head Injury in Mice
    Article Snippet: GLAST (biotin) , 1:11 , Mouse , IgG2a, K , NA , ASCA-1 , 130-118-984 , MACs (Miltenyi).

    Article Title: SOCS3 Regulates Dectin-2-Induced Inflammation in PBMCs of Diabetic Patients
    Article Snippet: Anti-CD45 VioBlue , IgG2a , 130-113-684 , Miltenyi Biotec.

    Article Title: Targeting Intracellular Innate RNA-Sensing Systems Overcomes Resistance to CAR T-cell Therapy in Solid Tumors
    Article Snippet: Alexa Fluor 647 murine cleaved Caspase-3 Rabbit IgG C92-605 BD BioSciences AB_1727414 Alexa Fluor 700 human Granzyme B Mouse IgG1, κ QA16A02 Biolegend AB_2728389 APC murine CD3 Rat IgG2b, κ 17A2 Biolegend AB_2561456 APC murine CD4 Rat IgG2b, κ GK1.5 Biolegend AB_312697 APC murine PD-1 Rat IgG2b, κ RMP1-30 Biolegend AB_10612938 APC murine Fas Mouse IgG1, κ 15A7 eBioscience AB_10717405 APC murine FasL Armenian Hamster IgG MFL3 Biolegend AB_2813951 APC murine Ki67 Rat IgG2a, κ 16A8 Biolegend AB_1727414 APC human CD3 Mouse IgG2a, κ OKT3 Biolegend AB_1937212 APC-Cy7 murine CD45.2 Mouse (SJL) IgG2a, κ 104 Biolegend AB_830789 APCeFluor 780 murine CD25 Rat IgG1, κ PC61.5 eBioscience AB_1272179 FITC murine CD3 Rat IgG2b, κ 17A2 Biolegend AB_312661 FITC murine c-myc Mouse IgG1 SH1-26E7.1.3 Miltenyi Biotec AB_2751329 FITC human CD8 Mouse IgG1, κ SK1 Biolegend AB_1877179 Pacific Blue murine CD4 Rat IgG2b, κ GK1.5 Biolegend AB_493647 Pacific Blue murine CD107a Rat IgG2a, κ 1D4B eBioscience AB_11219687 Pacific Blue murine Ki67 Rat IgG2a, κ 16A8 Biolegend AB_2564490 PE murine CD3 Rat IgG2b, κ 17A2 Biolegend AB_312663 PE murine IFN-g Rat IgG2a, κ XMG1.2 Biolegend AB_315402 PE murine CTLA-4 Armenian Hamster IgG UC10-4B9 Biolegend AB_313254 PE murine TRAILR2 (CD262) Armenian Hamster IgG MD5-1 Biolegend AB_345401 PE-Cy7 murine CD45.2 Mouse (SJL) IgG2a, κ 104 Biolegend AB_1186103 PE-Cy7 murine Granzyme B Rat IgG2a, κ NGZB eBioscience AB_10853339 PE-Cy7 murine TIM-3 Rat IgG1, κ B8.2C12 Biolegend AB_2632733 PerCPCy5.5 murine CD8 Rat IgG2a, κ 53-6.7 Biolegend AB_2075238 PerCPCy5.5 murine CD69 Armenian Hamster IgG H1.2F3 Biolegend AB_940495 PerCPCy5.5 murine LAG-3 Rat IgG1, κ C9B7W Biolegend AB_2561516 PerCPCy5.5 murine EpCAM Rat IgG2a, κ G8.8 Biolegend AB_2098647 PerCPCy5.5 murine Fas Mouse IgG1, κ SA367H8 Biolegend AB_2632904

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    Article Title: Complex Tumor Spheroid Formation and One-Step Cancer-Associated Fibroblasts Purification from Hepatocellular Carcinoma Tissue Promoted by Inorganic Surface Topography
    Article Snippet: .. Analysis of markers to detect HCC cancer cells and CAFs was performed using the following anti-human antibodies: Alexa Fluor 488-conjugated IgG2a to alpha-fetoprotein (AFP, BD Biosciences, San Jose, CA, USA); FITC-conjugated IgG1 to CD13 (Merck, Germany); FITC-conjugated IgG2b to CD44 (BD Biosciences, USA); FITC-conjugated IgG1 to CD90 (BD Biosciences, USA); FITC-conjugated IgG1 to CD133 (Miltenyi Biotec, Bergisch Gladbach, Germany); Unconjugated IgG1 to CD151 (abcam, Cambridge, UK); FITC-conjugated IgG2b to EpCAM (BioLegend, San Diego, CA, USA); Unconjugated IgG1 to OV-6 (R&D Systems, Minneapolis, MN, USA); FITC-conjugated IgG1, IgG2a and IgG2b isotype control antibodies (Miltenyi Biotec, Bergisch Gladbach, Germany); Alexa Fluor 488-conjugated IgG isotype control antibody (abcam, Cambridge, UK); Alexa Fluor 488-conjugated anti-mouse antibody. .. Briefly, the cells were detached using StemPro Accutase Cell Dissociation Reagent (Thermo Fisher Scientific, Waltham, MA, USA) and incubated with fluorophore-conjugated antibodies for surface staining of CD13, CD44, CD90, CD133, CD151, EpCAM, and OV-6 for 1 h at 4 °C in the dark.

    Article Title: Expression Profile of New Marker Genes Involved in Differentiation of Human Wharton’s Jelly-Derived Mesenchymal Stem Cells into Chondrocytes, Osteoblasts, Adipocytes and Neural-like Cells
    Article Snippet: Isotype control IgG1 , FITC , IgG1k , IS5-21F5 , Miltenyi Biotec. .. Isotype control IgG2a , PerCP , IgG2a , S43.10 , Miltenyi Biotec. .. Isotype control IgG2a , PE , IgG2a , S43.10 , Miltenyi Biotec.

    Article Title: Expression Profile of New Marker Genes Involved in Differentiation of Human Wharton’s Jelly-Derived Mesenchymal Stem Cells into Chondrocytes, Osteoblasts, Adipocytes and Neural-like Cells
    Article Snippet: Isotype control IgG2a , PerCP , IgG2a , S43.10 , Miltenyi Biotec. .. Isotype control IgG2a , PE , IgG2a , S43.10 , Miltenyi Biotec. .. REA Control (S) , APC , IgG1 , REA293 , Miltenyi Biotec.



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    CLCA4 suppressed colorectal cancer stem cell expansion by interacting with vimentin to suppress FAK signaling pathways. (A) Western blotting analysis of FAK and p-FAK protein levels in control and CLCA4-overexpressing colorectal cancer (CRC) cells. Right panels: Quantification of protein expression ratio. (B) Western blotting analysis of stemness-related proteins and p-FAK in CLCA4-overexpressing cells treated with or without FAK agonist. Lower panels: Quantification of protein expression ratio. (C) Tumorsphere formation assay was performed to examine the tumorsphere formation ability in CLCA4-overexpressing cells treated with or without FAK agonist. One-way ANOVA with Tukey's multiple comparisons test (mean ± standard deviation). (D) Immunoprecipitation and <t>IgG</t> samples were analyzed by mass spectrometry. Proteins with unused >1.3 were filtered out, and keratin was removed. A total of 336 proteins were identified, including 334 proteins in immunoprecipitation samples and 4 proteins in IgG samples. (E) The immunoprecipitates of CLCA4 were purified using anti-Flag antibody and separated with SDS-PAGE, and the presence of vimentin was analyzed by Western blotting. Normal IgG was used as the negative control. (F) The immunoprecipitates of vimentin were purified using anti-HA antibody and separated with SDS-PAGE, and the presence of CLCA4 was analyzed by Western blotting. Normal IgG was used as the negative control. (G) The differences in protein levels (vimentin, Bmi-1, and p-FAK) among CRC cells transfected with different plasmids were analyzed by Western blotting. Right panels: Quantification of protein expression ratio. (H) Tumorsphere formation assay was performed to examine the tumorsphere formation ability among CRC cells transfected with different plasmids. One-way ANOVA with Tukey's multiple comparisons test (mean ± standard deviation).
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    CLCA4 suppressed colorectal cancer stem cell expansion by interacting with vimentin to suppress FAK signaling pathways. (A) Western blotting analysis of FAK and p-FAK protein levels in control and CLCA4-overexpressing colorectal cancer (CRC) cells. Right panels: Quantification of protein expression ratio. (B) Western blotting analysis of stemness-related proteins and p-FAK in CLCA4-overexpressing cells treated with or without FAK agonist. Lower panels: Quantification of protein expression ratio. (C) Tumorsphere formation assay was performed to examine the tumorsphere formation ability in CLCA4-overexpressing cells treated with or without FAK agonist. One-way ANOVA with Tukey's multiple comparisons test (mean ± standard deviation). (D) Immunoprecipitation and IgG samples were analyzed by mass spectrometry. Proteins with unused >1.3 were filtered out, and keratin was removed. A total of 336 proteins were identified, including 334 proteins in immunoprecipitation samples and 4 proteins in IgG samples. (E) The immunoprecipitates of CLCA4 were purified using anti-Flag antibody and separated with SDS-PAGE, and the presence of vimentin was analyzed by Western blotting. Normal IgG was used as the negative control. (F) The immunoprecipitates of vimentin were purified using anti-HA antibody and separated with SDS-PAGE, and the presence of CLCA4 was analyzed by Western blotting. Normal IgG was used as the negative control. (G) The differences in protein levels (vimentin, Bmi-1, and p-FAK) among CRC cells transfected with different plasmids were analyzed by Western blotting. Right panels: Quantification of protein expression ratio. (H) Tumorsphere formation assay was performed to examine the tumorsphere formation ability among CRC cells transfected with different plasmids. One-way ANOVA with Tukey's multiple comparisons test (mean ± standard deviation).

    Journal: Genes & Diseases

    Article Title: Chloride channel accessory 4 suppresses stem cell-like properties of colorectal cancer and enhances anti-PD-1 immunotherapy

    doi: 10.1016/j.gendis.2025.101859

    Figure Lengend Snippet: CLCA4 suppressed colorectal cancer stem cell expansion by interacting with vimentin to suppress FAK signaling pathways. (A) Western blotting analysis of FAK and p-FAK protein levels in control and CLCA4-overexpressing colorectal cancer (CRC) cells. Right panels: Quantification of protein expression ratio. (B) Western blotting analysis of stemness-related proteins and p-FAK in CLCA4-overexpressing cells treated with or without FAK agonist. Lower panels: Quantification of protein expression ratio. (C) Tumorsphere formation assay was performed to examine the tumorsphere formation ability in CLCA4-overexpressing cells treated with or without FAK agonist. One-way ANOVA with Tukey's multiple comparisons test (mean ± standard deviation). (D) Immunoprecipitation and IgG samples were analyzed by mass spectrometry. Proteins with unused >1.3 were filtered out, and keratin was removed. A total of 336 proteins were identified, including 334 proteins in immunoprecipitation samples and 4 proteins in IgG samples. (E) The immunoprecipitates of CLCA4 were purified using anti-Flag antibody and separated with SDS-PAGE, and the presence of vimentin was analyzed by Western blotting. Normal IgG was used as the negative control. (F) The immunoprecipitates of vimentin were purified using anti-HA antibody and separated with SDS-PAGE, and the presence of CLCA4 was analyzed by Western blotting. Normal IgG was used as the negative control. (G) The differences in protein levels (vimentin, Bmi-1, and p-FAK) among CRC cells transfected with different plasmids were analyzed by Western blotting. Right panels: Quantification of protein expression ratio. (H) Tumorsphere formation assay was performed to examine the tumorsphere formation ability among CRC cells transfected with different plasmids. One-way ANOVA with Tukey's multiple comparisons test (mean ± standard deviation).

    Article Snippet: After 7 days, mice were intraperitoneally treated with either an in vivo blocking antibody against mouse PD-1 (Clone: 29F.1A2, BioXcell, Cat# BP0273) or a rat IgG2a isotype control antibody (Clone: 2A3, BioXcell, Cat# BP0089).

    Techniques: Protein-Protein interactions, Western Blot, Control, Expressing, Tube Formation Assay, Standard Deviation, Immunoprecipitation, Mass Spectrometry, Purification, SDS Page, Negative Control, Transfection