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anti-st2 mab  (R&D Systems)


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    Structured Review

    R&D Systems anti-st2 mab
    Levels of total IgG ( A ) and IgG1 ( B ) in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or <t>+anti-ST2:</t> the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.
    Anti St2 Mab, supplied by R&D Systems, 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/anti+st2+mab/anti+st2/pmc11125625-48-6-16
    Average 90 stars, based on 1 article reviews
    anti-st2 mab - by Bioz Stars, 2026-10
    90/100 stars

    Images

    1) Product Images from "IL-33 Enhances the Total Production of IgG, IgG1, and IgG3 in Angiostrongylus cantonensis -Infected Mice"

    Article Title: IL-33 Enhances the Total Production of IgG, IgG1, and IgG3 in Angiostrongylus cantonensis -Infected Mice

    Journal: Tropical Medicine and Infectious Disease

    doi: 10.3390/tropicalmed9050111

    Levels of total IgG ( A ) and IgG1 ( B ) in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.
    Figure Legend Snippet: Levels of total IgG ( A ) and IgG1 ( B ) in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Techniques Used: Infection

    Levels of IgG2a ( A ), IgG2b ( B ), IgG2c ( C ), and IgG3 ( D ) in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.
    Figure Legend Snippet: Levels of IgG2a ( A ), IgG2b ( B ), IgG2c ( C ), and IgG3 ( D ) in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Techniques Used: Infection

    Levels of IgE in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.
    Figure Legend Snippet: Levels of IgE in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Techniques Used: Infection

    The proportion of each IgG subclass in the sum of IgG1 (1), IgG2 subtypes (2a, 2b, and 2c), and IgG3 (3) in each group. The blood samples were collected at the 3rd week post-infection. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.
    Figure Legend Snippet: The proportion of each IgG subclass in the sum of IgG1 (1), IgG2 subtypes (2a, 2b, and 2c), and IgG3 (3) in each group. The blood samples were collected at the 3rd week post-infection. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Techniques Used: Infection

    The proportion of each IgG subclass in the sum of IgG1 (1), IgG2 subtypes (2a, 2b, and 2c), and IgG3 (3) in each group. The blood samples were collected at the 4th week post-infection. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.
    Figure Legend Snippet: The proportion of each IgG subclass in the sum of IgG1 (1), IgG2 subtypes (2a, 2b, and 2c), and IgG3 (3) in each group. The blood samples were collected at the 4th week post-infection. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Techniques Used: Infection

    Related Articles

    Injection:

    Article Title: sST2: A Bridge Between Sirt1/p53/p21 Signal-Induced Senescence and TGF-β1/Smad2/3 Regulation of Cardiac Fibrosis in Mouse Viral Myocarditis
    Article Snippet: .. Anti-ST2 mAb (R&D systems, MAB10041) were given to VMC mice by intraperitoneal ( i.p. ) injection the day before and the day after the infection (20 μg/mouse). ..

    Article Title: sST2: A Bridge Between Sirt1/p53/p21 Signal-Induced Senescence and TGF-β1/Smad2/3 Regulation of Cardiac Fibrosis in Mouse Viral Myocarditis.
    Article Snippet: .. Anti-ST2 mAb (R&D systems, MAB10041) were given to VMC mice by intraperitoneal (i.p.) injection the day before and the day after the infection (20 μg/mouse). ..

    Infection:

    Article Title: sST2: A Bridge Between Sirt1/p53/p21 Signal-Induced Senescence and TGF-β1/Smad2/3 Regulation of Cardiac Fibrosis in Mouse Viral Myocarditis
    Article Snippet: .. Anti-ST2 mAb (R&D systems, MAB10041) were given to VMC mice by intraperitoneal ( i.p. ) injection the day before and the day after the infection (20 μg/mouse). ..

    Article Title: sST2: A Bridge Between Sirt1/p53/p21 Signal-Induced Senescence and TGF-β1/Smad2/3 Regulation of Cardiac Fibrosis in Mouse Viral Myocarditis.
    Article Snippet: .. Anti-ST2 mAb (R&D systems, MAB10041) were given to VMC mice by intraperitoneal (i.p.) injection the day before and the day after the infection (20 μg/mouse). ..

    Neutralization:

    Article Title: Stromal interleukin-33 promotes regulatory T cell-mediated immunosuppression in head and neck squamous cell carcinoma and correlates with poor prognosis.
    Article Snippet: Regulatory T cells (Tregs) mediate immunosuppressive signals that can contribute to the progression of head and neck squamous cell carcinoma (HNSCC).. Interleukin-33 (IL-33) is defined as an ‘alarmin’, an endogenous factor that is expressed during tissue and cell damage, which has been shown to promote Treg proliferation in non-lymphoid organs.. However, the interaction between IL-33 and Tregs in the HNSCC tumor microenvironment remains uncertain.

    Article Title: Stromal interleukin-33 promotes regulatory T cell-mediated immunosuppression in head and neck squamous cell carcinoma and correlates with poor prognosis
    Article Snippet: For Treg cell generation, SNU899 TSN-stimulated DCs were added to CD4 + T cells at a ratio of 1:10 and co-cultured for 5 days with 2 μg/ml anti-CD3 (555336, BD Bioscience) with or without 1 ng/ml recombinant human IL-33 (3625-IL-010, R&D System). .. For neutralization experiments, a human anti-ST2 mAb (3 μg/ml, AF523, R&D Systems) was added at the start of the co-culture. ..

    Control:

    Article Title: An IL-1 cytokine member, IL-33, induces human basophil activation via its ST2 receptor.
    Article Snippet: Human IL-3 was donated by the Kirin Brewery. .. The following Abs were purchased as indicated: mouse anti-IL-4 mAb (IgG1, clone 8D4–8) and biotin-conjugated rat anti-IL-4 mAb (IgG1, clone MP4–25D2) (eBioscience); FITC-conjugated goat anti-human IgE Ab (Biosource International); mouse neutralizing anti-ST2 mAb (IgG1, clone 97203) (R&D Systems); rabbit anti-IL-33 pAb (Adipogen); mouse anti-ST2 mAb (IgG1, clone HB12) (MBL); control mouse IgG1 (MOPC21) and mouse IgG2a (UPC10) (Sigma-Aldrich); mouse IgG2b mAb (MOPC 195) (Cappel); and FITC-conjugated goat anti-mouse IgG (Jackson ImmunoResearch). ..

    other:

    Article Title: GROUP 2 INNATE LYMPHOID CELLS AND CD4 + T CELLS COOPERATE TO MEDIATE TYPE 2 IMMUNE RESPONSE IN MICE
    Article Snippet: Anti-ST2 mAb (97203) was from R&D Systems.



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    Levels of total IgG ( A ) and IgG1 ( B ) in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or <t>+anti-ST2:</t> the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.
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    Image Search Results


    Levels of total IgG ( A ) and IgG1 ( B ) in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Journal: Tropical Medicine and Infectious Disease

    Article Title: IL-33 Enhances the Total Production of IgG, IgG1, and IgG3 in Angiostrongylus cantonensis -Infected Mice

    doi: 10.3390/tropicalmed9050111

    Figure Lengend Snippet: Levels of total IgG ( A ) and IgG1 ( B ) in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Article Snippet: The dose of anti-IL-33 mAb and anti-ST2 mAb is 10 µg in 0.1 mL of PBS (R&D Systems Inc., USA) and 50 µg in 0.1 mL of PBS (R&D Systems Inc., USA), respectively.

    Techniques: Infection

    Levels of IgG2a ( A ), IgG2b ( B ), IgG2c ( C ), and IgG3 ( D ) in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Journal: Tropical Medicine and Infectious Disease

    Article Title: IL-33 Enhances the Total Production of IgG, IgG1, and IgG3 in Angiostrongylus cantonensis -Infected Mice

    doi: 10.3390/tropicalmed9050111

    Figure Lengend Snippet: Levels of IgG2a ( A ), IgG2b ( B ), IgG2c ( C ), and IgG3 ( D ) in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Article Snippet: The dose of anti-IL-33 mAb and anti-ST2 mAb is 10 µg in 0.1 mL of PBS (R&D Systems Inc., USA) and 50 µg in 0.1 mL of PBS (R&D Systems Inc., USA), respectively.

    Techniques: Infection

    Levels of IgE in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Journal: Tropical Medicine and Infectious Disease

    Article Title: IL-33 Enhances the Total Production of IgG, IgG1, and IgG3 in Angiostrongylus cantonensis -Infected Mice

    doi: 10.3390/tropicalmed9050111

    Figure Lengend Snippet: Levels of IgE in the sera of mice. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Article Snippet: The dose of anti-IL-33 mAb and anti-ST2 mAb is 10 µg in 0.1 mL of PBS (R&D Systems Inc., USA) and 50 µg in 0.1 mL of PBS (R&D Systems Inc., USA), respectively.

    Techniques: Infection

    The proportion of each IgG subclass in the sum of IgG1 (1), IgG2 subtypes (2a, 2b, and 2c), and IgG3 (3) in each group. The blood samples were collected at the 3rd week post-infection. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Journal: Tropical Medicine and Infectious Disease

    Article Title: IL-33 Enhances the Total Production of IgG, IgG1, and IgG3 in Angiostrongylus cantonensis -Infected Mice

    doi: 10.3390/tropicalmed9050111

    Figure Lengend Snippet: The proportion of each IgG subclass in the sum of IgG1 (1), IgG2 subtypes (2a, 2b, and 2c), and IgG3 (3) in each group. The blood samples were collected at the 3rd week post-infection. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Article Snippet: The dose of anti-IL-33 mAb and anti-ST2 mAb is 10 µg in 0.1 mL of PBS (R&D Systems Inc., USA) and 50 µg in 0.1 mL of PBS (R&D Systems Inc., USA), respectively.

    Techniques: Infection

    The proportion of each IgG subclass in the sum of IgG1 (1), IgG2 subtypes (2a, 2b, and 2c), and IgG3 (3) in each group. The blood samples were collected at the 4th week post-infection. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Journal: Tropical Medicine and Infectious Disease

    Article Title: IL-33 Enhances the Total Production of IgG, IgG1, and IgG3 in Angiostrongylus cantonensis -Infected Mice

    doi: 10.3390/tropicalmed9050111

    Figure Lengend Snippet: The proportion of each IgG subclass in the sum of IgG1 (1), IgG2 subtypes (2a, 2b, and 2c), and IgG3 (3) in each group. The blood samples were collected at the 4th week post-infection. N: non-infected mice. Ac: A. cantonensis -infected mice. +IL-33: the mice received injections of IL-33. +anti-IL-33 or +anti-ST2: the mice received injections of anti-IL-33 mAb or anti-ST2 mAb. The injections began at 3 dpi and subsequent booster injections were administered at 5-day intervals with the same dose.

    Article Snippet: The dose of anti-IL-33 mAb and anti-ST2 mAb is 10 µg in 0.1 mL of PBS (R&D Systems Inc., USA) and 50 µg in 0.1 mL of PBS (R&D Systems Inc., USA), respectively.

    Techniques: Infection

    IL-33 restored the suppressive function of Tregs, inhibited the production of interferon (IFN)-γ by regulatory T cells (Tregs) and the activation of orbital fibroblasts (OFs) in idiopathic orbital inflammation (IOI). (A) The plasma level of interleukin (IL)-33 in healthy controls (n = 18) and patients with IOI (n = 22) was assessed by Luminex technology. (B) The proportion of circulating ST2 + Foxp3 + Tregs in healthy controls (n = 14) and patients with IOI (n = 8). (C) IL-33 and (D) IL1RL1 mRNA expression in orbital fat from healthy subjects (n = 4) and patients with IOI (n = 15). (E) Intracellular cytokines secreted by FACS-sorted Tregs from IOI patients (n = 5) were detected after stimulation with IL-33 in the presence of anti-CD3 and anti-CD28 and IL-2. (F) Proliferation of CFSE labeled naïve T cells cocultured with sorted-Tregs under different treatment conditions. (G) Expression of a-SMA in OFs cocultured with Tregs under different treatment conditions. * P < 0.05; ** P < 0.01; *** P < 0.001; **** P < 0.0001; ns, not significant.

    Journal: Frontiers in Immunology

    Article Title: Increased Dysfunctional and Plastic Regulatory T Cells in Idiopathic Orbital Inflammation

    doi: 10.3389/fimmu.2021.634847

    Figure Lengend Snippet: IL-33 restored the suppressive function of Tregs, inhibited the production of interferon (IFN)-γ by regulatory T cells (Tregs) and the activation of orbital fibroblasts (OFs) in idiopathic orbital inflammation (IOI). (A) The plasma level of interleukin (IL)-33 in healthy controls (n = 18) and patients with IOI (n = 22) was assessed by Luminex technology. (B) The proportion of circulating ST2 + Foxp3 + Tregs in healthy controls (n = 14) and patients with IOI (n = 8). (C) IL-33 and (D) IL1RL1 mRNA expression in orbital fat from healthy subjects (n = 4) and patients with IOI (n = 15). (E) Intracellular cytokines secreted by FACS-sorted Tregs from IOI patients (n = 5) were detected after stimulation with IL-33 in the presence of anti-CD3 and anti-CD28 and IL-2. (F) Proliferation of CFSE labeled naïve T cells cocultured with sorted-Tregs under different treatment conditions. (G) Expression of a-SMA in OFs cocultured with Tregs under different treatment conditions. * P < 0.05; ** P < 0.01; *** P < 0.001; **** P < 0.0001; ns, not significant.

    Article Snippet: In some experiments of CFSE assay and cytokine measurement, Tregs were stimulated with recombinant human (rh)IL-33 (20 ng/mL) (R&D Systems) and human anti-ST2 mAb (R&D Systems), which competitively bound to the IL-33 receptor (ST2).

    Techniques: Activation Assay, Clinical Proteomics, Luminex, Expressing, Labeling