mouse igg2a isotype control antibody Search Results


95
Miltenyi Biotec mouse igg2a isotype control fitc

Mouse Igg2a Isotype Control Fitc, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Bio-Techne corporation isotype control

Isotype Control, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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Proteintech ab277236 igg isotype control primary mouse

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Proteintech conjugated mouse igg2a isotype control

Conjugated Mouse Igg2a Isotype Control, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Vasculox Inc isotype matched-control mouse immunoglobulin g 2a (igg2a) antibody

Isotype Matched Control Mouse Immunoglobulin G 2a (Igg2a) Antibody, supplied by Vasculox Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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Novimmune isotype-matched control mab, w6/32
Toll-like receptor 4 (TLR4) drives systemic inflammation and end-organ damage in a mouse model of hemorrhagic shock (HS) and trauma (HS/T). Wild-type (WT), TLR4 −/− , MyD88 −/− , or Trif −/− B6 mice were subjected to HS/T. IL-6 and ALT plasma levels were measured 6 h after the onset of HS/T as described in Section “ ” (A,B) . In separate experiments, the selective anti-mouse TLR4 Ab 1A6 or its isotype control <t>(W6/32</t> Ab) was administered intravenously 30 min prior to the initiation of the HS and the levels of IL-6 and ALT were measured at 3, 6, and 20 h after the onset of HS/T (C,D) . Panels (A,C) show IL-6 plasma levels, (B,D) show ALT plasma levels, (E,F) show IL-6 and ALT plasma levels after 6 h following the initiation of HS/T in the following cell-specific TLR4 −/− B6 mouse strains: Albumin-Cre × TLR4 loxP/loxP (Alb-Cre), CD11c-Cre × TLR4 loxP/loxP (CD11c-Cre), and Lyz-Cre × TLR4 loxP/loxP (Lyz-Cre). WT and TLR4 loxP/loxP (FloxP) mice were used as controls. Panels (G,H) show IL-6 and ALT plasma levels in lethally irradiated WT B6 mice reconstituted with bone marrow cells from CD11c-diphtheria toxin (DT) receptor (DTR) B6 mice or CD11c-TLR4 −/− B6 mice at 6 h after HS/T. WT B6 mice were used as controls [ (A,B,E,F) * P < 0.05, analyzed by Mann–Whitney Rank Sum Test; (C) P = 0.050, (D) * P < 0.001, analyzed by two-way ANOVA; (G,H) * P < 0.001, analyzed by Student’s t -test ( n = 6–15 animals/experimental condition)].
Isotype Matched Control Mab, W6/32, supplied by Novimmune, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+igg2a+isotype+control+antibody/pmc05712321-63-11-15?v=Novimmune
Average 90 stars, based on 1 article reviews
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Bio-Techne corporation mouse igg2a alexa fluor® 488-conjugated antibody
Toll-like receptor 4 (TLR4) drives systemic inflammation and end-organ damage in a mouse model of hemorrhagic shock (HS) and trauma (HS/T). Wild-type (WT), TLR4 −/− , MyD88 −/− , or Trif −/− B6 mice were subjected to HS/T. IL-6 and ALT plasma levels were measured 6 h after the onset of HS/T as described in Section “ ” (A,B) . In separate experiments, the selective anti-mouse TLR4 Ab 1A6 or its isotype control <t>(W6/32</t> Ab) was administered intravenously 30 min prior to the initiation of the HS and the levels of IL-6 and ALT were measured at 3, 6, and 20 h after the onset of HS/T (C,D) . Panels (A,C) show IL-6 plasma levels, (B,D) show ALT plasma levels, (E,F) show IL-6 and ALT plasma levels after 6 h following the initiation of HS/T in the following cell-specific TLR4 −/− B6 mouse strains: Albumin-Cre × TLR4 loxP/loxP (Alb-Cre), CD11c-Cre × TLR4 loxP/loxP (CD11c-Cre), and Lyz-Cre × TLR4 loxP/loxP (Lyz-Cre). WT and TLR4 loxP/loxP (FloxP) mice were used as controls. Panels (G,H) show IL-6 and ALT plasma levels in lethally irradiated WT B6 mice reconstituted with bone marrow cells from CD11c-diphtheria toxin (DT) receptor (DTR) B6 mice or CD11c-TLR4 −/− B6 mice at 6 h after HS/T. WT B6 mice were used as controls [ (A,B,E,F) * P < 0.05, analyzed by Mann–Whitney Rank Sum Test; (C) P = 0.050, (D) * P < 0.001, analyzed by two-way ANOVA; (G,H) * P < 0.001, analyzed by Student’s t -test ( n = 6–15 animals/experimental condition)].
Mouse Igg2a Alexa Fluor® 488 Conjugated Antibody, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 92 stars, based on 1 article reviews
mouse igg2a alexa fluor® 488-conjugated antibody - by Bioz Stars, 2026-07
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96
Bio-Techne corporation mouse igg2a fluorescein-conjugated antibody
Toll-like receptor 4 (TLR4) drives systemic inflammation and end-organ damage in a mouse model of hemorrhagic shock (HS) and trauma (HS/T). Wild-type (WT), TLR4 −/− , MyD88 −/− , or Trif −/− B6 mice were subjected to HS/T. IL-6 and ALT plasma levels were measured 6 h after the onset of HS/T as described in Section “ ” (A,B) . In separate experiments, the selective anti-mouse TLR4 Ab 1A6 or its isotype control <t>(W6/32</t> Ab) was administered intravenously 30 min prior to the initiation of the HS and the levels of IL-6 and ALT were measured at 3, 6, and 20 h after the onset of HS/T (C,D) . Panels (A,C) show IL-6 plasma levels, (B,D) show ALT plasma levels, (E,F) show IL-6 and ALT plasma levels after 6 h following the initiation of HS/T in the following cell-specific TLR4 −/− B6 mouse strains: Albumin-Cre × TLR4 loxP/loxP (Alb-Cre), CD11c-Cre × TLR4 loxP/loxP (CD11c-Cre), and Lyz-Cre × TLR4 loxP/loxP (Lyz-Cre). WT and TLR4 loxP/loxP (FloxP) mice were used as controls. Panels (G,H) show IL-6 and ALT plasma levels in lethally irradiated WT B6 mice reconstituted with bone marrow cells from CD11c-diphtheria toxin (DT) receptor (DTR) B6 mice or CD11c-TLR4 −/− B6 mice at 6 h after HS/T. WT B6 mice were used as controls [ (A,B,E,F) * P < 0.05, analyzed by Mann–Whitney Rank Sum Test; (C) P = 0.050, (D) * P < 0.001, analyzed by two-way ANOVA; (G,H) * P < 0.001, analyzed by Student’s t -test ( n = 6–15 animals/experimental condition)].
Mouse Igg2a Fluorescein Conjugated Antibody, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
mouse igg2a fluorescein-conjugated antibody - by Bioz Stars, 2026-07
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90
MultiSciences Biotech Co Ltd mouse igg2a isotype control, apc antibody
Toll-like receptor 4 (TLR4) drives systemic inflammation and end-organ damage in a mouse model of hemorrhagic shock (HS) and trauma (HS/T). Wild-type (WT), TLR4 −/− , MyD88 −/− , or Trif −/− B6 mice were subjected to HS/T. IL-6 and ALT plasma levels were measured 6 h after the onset of HS/T as described in Section “ ” (A,B) . In separate experiments, the selective anti-mouse TLR4 Ab 1A6 or its isotype control <t>(W6/32</t> Ab) was administered intravenously 30 min prior to the initiation of the HS and the levels of IL-6 and ALT were measured at 3, 6, and 20 h after the onset of HS/T (C,D) . Panels (A,C) show IL-6 plasma levels, (B,D) show ALT plasma levels, (E,F) show IL-6 and ALT plasma levels after 6 h following the initiation of HS/T in the following cell-specific TLR4 −/− B6 mouse strains: Albumin-Cre × TLR4 loxP/loxP (Alb-Cre), CD11c-Cre × TLR4 loxP/loxP (CD11c-Cre), and Lyz-Cre × TLR4 loxP/loxP (Lyz-Cre). WT and TLR4 loxP/loxP (FloxP) mice were used as controls. Panels (G,H) show IL-6 and ALT plasma levels in lethally irradiated WT B6 mice reconstituted with bone marrow cells from CD11c-diphtheria toxin (DT) receptor (DTR) B6 mice or CD11c-TLR4 −/− B6 mice at 6 h after HS/T. WT B6 mice were used as controls [ (A,B,E,F) * P < 0.05, analyzed by Mann–Whitney Rank Sum Test; (C) P = 0.050, (D) * P < 0.001, analyzed by two-way ANOVA; (G,H) * P < 0.001, analyzed by Student’s t -test ( n = 6–15 animals/experimental condition)].
Mouse Igg2a Isotype Control, Apc Antibody, supplied by MultiSciences Biotech Co Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+igg2a+isotype+control+antibody/pm30763585-56-47-55?v=MultiSciences+Biotech+Co+Ltd
Average 90 stars, based on 1 article reviews
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Galaxy Biotech isotype-matched control antibody (mouse igg2a)
Toll-like receptor 4 (TLR4) drives systemic inflammation and end-organ damage in a mouse model of hemorrhagic shock (HS) and trauma (HS/T). Wild-type (WT), TLR4 −/− , MyD88 −/− , or Trif −/− B6 mice were subjected to HS/T. IL-6 and ALT plasma levels were measured 6 h after the onset of HS/T as described in Section “ ” (A,B) . In separate experiments, the selective anti-mouse TLR4 Ab 1A6 or its isotype control <t>(W6/32</t> Ab) was administered intravenously 30 min prior to the initiation of the HS and the levels of IL-6 and ALT were measured at 3, 6, and 20 h after the onset of HS/T (C,D) . Panels (A,C) show IL-6 plasma levels, (B,D) show ALT plasma levels, (E,F) show IL-6 and ALT plasma levels after 6 h following the initiation of HS/T in the following cell-specific TLR4 −/− B6 mouse strains: Albumin-Cre × TLR4 loxP/loxP (Alb-Cre), CD11c-Cre × TLR4 loxP/loxP (CD11c-Cre), and Lyz-Cre × TLR4 loxP/loxP (Lyz-Cre). WT and TLR4 loxP/loxP (FloxP) mice were used as controls. Panels (G,H) show IL-6 and ALT plasma levels in lethally irradiated WT B6 mice reconstituted with bone marrow cells from CD11c-diphtheria toxin (DT) receptor (DTR) B6 mice or CD11c-TLR4 −/− B6 mice at 6 h after HS/T. WT B6 mice were used as controls [ (A,B,E,F) * P < 0.05, analyzed by Mann–Whitney Rank Sum Test; (C) P = 0.050, (D) * P < 0.001, analyzed by two-way ANOVA; (G,H) * P < 0.001, analyzed by Student’s t -test ( n = 6–15 animals/experimental condition)].
Isotype Matched Control Antibody (Mouse Igg2a), supplied by Galaxy Biotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+igg2a+isotype+control+antibody/pm17307814-48-22-7?v=Galaxy+Biotech
Average 90 stars, based on 1 article reviews
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Isotype Note IgG2a kappa Host Species Note Mouse BALB c
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Image Search Results


Journal: iScience

Article Title: Migration of human T cells can be differentially directed by electric fields depending on the extracellular microenvironment

doi: 10.1016/j.isci.2024.109746

Figure Lengend Snippet:

Article Snippet: Mouse IgG2a isotype control - FITC , Miltenyi Biotec , Cat#: 130-113-271 Lot: 5200908299.

Techniques: Recombinant, Control, Cell Isolation, Isolation, Software

Toll-like receptor 4 (TLR4) drives systemic inflammation and end-organ damage in a mouse model of hemorrhagic shock (HS) and trauma (HS/T). Wild-type (WT), TLR4 −/− , MyD88 −/− , or Trif −/− B6 mice were subjected to HS/T. IL-6 and ALT plasma levels were measured 6 h after the onset of HS/T as described in Section “ ” (A,B) . In separate experiments, the selective anti-mouse TLR4 Ab 1A6 or its isotype control (W6/32 Ab) was administered intravenously 30 min prior to the initiation of the HS and the levels of IL-6 and ALT were measured at 3, 6, and 20 h after the onset of HS/T (C,D) . Panels (A,C) show IL-6 plasma levels, (B,D) show ALT plasma levels, (E,F) show IL-6 and ALT plasma levels after 6 h following the initiation of HS/T in the following cell-specific TLR4 −/− B6 mouse strains: Albumin-Cre × TLR4 loxP/loxP (Alb-Cre), CD11c-Cre × TLR4 loxP/loxP (CD11c-Cre), and Lyz-Cre × TLR4 loxP/loxP (Lyz-Cre). WT and TLR4 loxP/loxP (FloxP) mice were used as controls. Panels (G,H) show IL-6 and ALT plasma levels in lethally irradiated WT B6 mice reconstituted with bone marrow cells from CD11c-diphtheria toxin (DT) receptor (DTR) B6 mice or CD11c-TLR4 −/− B6 mice at 6 h after HS/T. WT B6 mice were used as controls [ (A,B,E,F) * P < 0.05, analyzed by Mann–Whitney Rank Sum Test; (C) P = 0.050, (D) * P < 0.001, analyzed by two-way ANOVA; (G,H) * P < 0.001, analyzed by Student’s t -test ( n = 6–15 animals/experimental condition)].

Journal: Frontiers in Immunology

Article Title: Toll-Like Receptor 4 on both Myeloid Cells and Dendritic Cells Is Required for Systemic Inflammation and Organ Damage after Hemorrhagic Shock with Tissue Trauma in Mice

doi: 10.3389/fimmu.2017.01672

Figure Lengend Snippet: Toll-like receptor 4 (TLR4) drives systemic inflammation and end-organ damage in a mouse model of hemorrhagic shock (HS) and trauma (HS/T). Wild-type (WT), TLR4 −/− , MyD88 −/− , or Trif −/− B6 mice were subjected to HS/T. IL-6 and ALT plasma levels were measured 6 h after the onset of HS/T as described in Section “ ” (A,B) . In separate experiments, the selective anti-mouse TLR4 Ab 1A6 or its isotype control (W6/32 Ab) was administered intravenously 30 min prior to the initiation of the HS and the levels of IL-6 and ALT were measured at 3, 6, and 20 h after the onset of HS/T (C,D) . Panels (A,C) show IL-6 plasma levels, (B,D) show ALT plasma levels, (E,F) show IL-6 and ALT plasma levels after 6 h following the initiation of HS/T in the following cell-specific TLR4 −/− B6 mouse strains: Albumin-Cre × TLR4 loxP/loxP (Alb-Cre), CD11c-Cre × TLR4 loxP/loxP (CD11c-Cre), and Lyz-Cre × TLR4 loxP/loxP (Lyz-Cre). WT and TLR4 loxP/loxP (FloxP) mice were used as controls. Panels (G,H) show IL-6 and ALT plasma levels in lethally irradiated WT B6 mice reconstituted with bone marrow cells from CD11c-diphtheria toxin (DT) receptor (DTR) B6 mice or CD11c-TLR4 −/− B6 mice at 6 h after HS/T. WT B6 mice were used as controls [ (A,B,E,F) * P < 0.05, analyzed by Mann–Whitney Rank Sum Test; (C) P = 0.050, (D) * P < 0.001, analyzed by two-way ANOVA; (G,H) * P < 0.001, analyzed by Student’s t -test ( n = 6–15 animals/experimental condition)].

Article Snippet: Anti-mouse TLR4 monoclonal antibody (mAb), 1A6, and its isotype-matched control mAb, W6/32, were provided by NovImmune SA (Geneva, Switzerland) and have been described previously ( ).

Techniques: Irradiation, MANN-WHITNEY