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lom612  (TargetMol)


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    TargetMol lom612
    Lom612, supplied by TargetMol, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/lom612/product/TargetMol
    Average 93 stars, based on 1 article reviews
    lom612 - by Bioz Stars, 2026-02
    93/100 stars

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    ( A ) Overview of VISTA downstream signaling. ( B – E ) Freshly isolated WT and Vsir –/– aILC2s were stained intranuclearly for p-AKT, FOXO1, p65, and p52. Representative histograms of protein expression of p-AKT ( B ), FOXO1 ( C ), p65 ( D ), and p52 ( E ), and corresponding quantifications as MFI. ( F – I ) WT aILC2s were treated with FOXO1 inhibitor or vehicle. ( G and H ) Representative plots of GATA-3 ( G ) and Ki67 ( H ) expression levels and corresponding quantification (as MFI). ( I ) Cytokine levels in cell supernatant (per 10 3 ILC2s). ( J – M ) WT aILC2s were treated with FOXO1 activator or vehicle. ( K and L ) Representative plots of GATA-3 ( K ) and Ki67 ( L ) expression levels and corresponding quantification (as MFI). ( M ) Cytokine levels in cell supernatant (per 10 3 ILC2s). Data are presented as mean + SEM and are representative of at least 2 independent experiments. Statistical significance was assessed using 2-tailed Student’s t test; ** P < 0.01, *** P < 0.001, **** P < 0.0001.

    Journal: The Journal of Clinical Investigation

    Article Title: FOXO1 pathway activation by VISTA immune checkpoint restrains pulmonary ILC2 functions

    doi: 10.1172/JCI184932

    Figure Lengend Snippet: ( A ) Overview of VISTA downstream signaling. ( B – E ) Freshly isolated WT and Vsir –/– aILC2s were stained intranuclearly for p-AKT, FOXO1, p65, and p52. Representative histograms of protein expression of p-AKT ( B ), FOXO1 ( C ), p65 ( D ), and p52 ( E ), and corresponding quantifications as MFI. ( F – I ) WT aILC2s were treated with FOXO1 inhibitor or vehicle. ( G and H ) Representative plots of GATA-3 ( G ) and Ki67 ( H ) expression levels and corresponding quantification (as MFI). ( I ) Cytokine levels in cell supernatant (per 10 3 ILC2s). ( J – M ) WT aILC2s were treated with FOXO1 activator or vehicle. ( K and L ) Representative plots of GATA-3 ( K ) and Ki67 ( L ) expression levels and corresponding quantification (as MFI). ( M ) Cytokine levels in cell supernatant (per 10 3 ILC2s). Data are presented as mean + SEM and are representative of at least 2 independent experiments. Statistical significance was assessed using 2-tailed Student’s t test; ** P < 0.01, *** P < 0.001, **** P < 0.0001.

    Article Snippet: When specified, 10 μg/mL VISTA agonist antibody (MH5A, BioLegend), 10 μg/mL VISTA antagonist antibody (13F3, Bio X Cell), 100 nM FOXO1 inhibitor (AS1842856, MedChemExpress), or 1 μM FOXO1 activator (LOM612, MedChemExpress) with corresponding isotype control or vehicle (DMSO) was further added to cultures for the indicated times.

    Techniques: Isolation, Staining, Expressing

    ( A – F ) Human peripheral ILC2s (hILC2s) were stimulated with or without rhIL-33 (100 ng/mL). ( B ) Representative plots of VISTA expression levels and corresponding quantification (as MFI). ( C – F ) hILC2s were treated with 5 μg/mL rhVSIG3 and vehicle control. ( C and D ) Representative plots of GATA-3 ( C ) and Ki67 ( D ) expression levels and corresponding quantification (as MFI). ( E ) Cytokine levels in hILC2 supernatant (per 10 3 ILC2s). ( F ) Representative plots of FOXO1 expression levels and corresponding quantification (as MFI) following 1 hour treatment with rhVSIG3. ( G – J ) A total of 2 × 10 5 hILC2s were transferred intravenously into Rag2 –/– GC –/– mice, followed by intranasal challenge with rhIL-33. On days 1 and 3, mice intravenously received 2 mg/kg rhVSIG3 or vehicle. ( H ) Lung resistance in response to elevating doses of methacholine. ( I ) Total number of ILC2s per lung. ( J ) Total number of eosinophils in BAL fluid. Data are presented as mean + SEM and are representative of at least 2 independent experiments. Statistical significance was assessed using either 2-tailed Student’s t test ( B – F , I , and J ) or 1-way ANOVA followed by Tukey’s post hoc test ( H ); * P < 0.05, ** P < 0.01.

    Journal: The Journal of Clinical Investigation

    Article Title: FOXO1 pathway activation by VISTA immune checkpoint restrains pulmonary ILC2 functions

    doi: 10.1172/JCI184932

    Figure Lengend Snippet: ( A – F ) Human peripheral ILC2s (hILC2s) were stimulated with or without rhIL-33 (100 ng/mL). ( B ) Representative plots of VISTA expression levels and corresponding quantification (as MFI). ( C – F ) hILC2s were treated with 5 μg/mL rhVSIG3 and vehicle control. ( C and D ) Representative plots of GATA-3 ( C ) and Ki67 ( D ) expression levels and corresponding quantification (as MFI). ( E ) Cytokine levels in hILC2 supernatant (per 10 3 ILC2s). ( F ) Representative plots of FOXO1 expression levels and corresponding quantification (as MFI) following 1 hour treatment with rhVSIG3. ( G – J ) A total of 2 × 10 5 hILC2s were transferred intravenously into Rag2 –/– GC –/– mice, followed by intranasal challenge with rhIL-33. On days 1 and 3, mice intravenously received 2 mg/kg rhVSIG3 or vehicle. ( H ) Lung resistance in response to elevating doses of methacholine. ( I ) Total number of ILC2s per lung. ( J ) Total number of eosinophils in BAL fluid. Data are presented as mean + SEM and are representative of at least 2 independent experiments. Statistical significance was assessed using either 2-tailed Student’s t test ( B – F , I , and J ) or 1-way ANOVA followed by Tukey’s post hoc test ( H ); * P < 0.05, ** P < 0.01.

    Article Snippet: When specified, 10 μg/mL VISTA agonist antibody (MH5A, BioLegend), 10 μg/mL VISTA antagonist antibody (13F3, Bio X Cell), 100 nM FOXO1 inhibitor (AS1842856, MedChemExpress), or 1 μM FOXO1 activator (LOM612, MedChemExpress) with corresponding isotype control or vehicle (DMSO) was further added to cultures for the indicated times.

    Techniques: Expressing, Control

    ( A ) Overview of VISTA downstream signaling. ( B – E ) Freshly isolated WT and Vsir –/– aILC2s were stained intranuclearly for p-AKT, FOXO1, p65, and p52. Representative histograms of protein expression of p-AKT ( B ), FOXO1 ( C ), p65 ( D ), and p52 ( E ), and corresponding quantifications as MFI. ( F – I ) WT aILC2s were treated with FOXO1 inhibitor or vehicle. ( G and H ) Representative plots of GATA-3 ( G ) and Ki67 ( H ) expression levels and corresponding quantification (as MFI). ( I ) Cytokine levels in cell supernatant (per 10 3 ILC2s). ( J – M ) WT aILC2s were treated with FOXO1 activator or vehicle. ( K and L ) Representative plots of GATA-3 ( K ) and Ki67 ( L ) expression levels and corresponding quantification (as MFI). ( M ) Cytokine levels in cell supernatant (per 10 3 ILC2s). Data are presented as mean + SEM and are representative of at least 2 independent experiments. Statistical significance was assessed using 2-tailed Student’s t test; ** P < 0.01, *** P < 0.001, **** P < 0.0001.

    Journal: The Journal of Clinical Investigation

    Article Title: FOXO1 pathway activation by VISTA immune checkpoint restrains pulmonary ILC2 functions

    doi: 10.1172/JCI184932

    Figure Lengend Snippet: ( A ) Overview of VISTA downstream signaling. ( B – E ) Freshly isolated WT and Vsir –/– aILC2s were stained intranuclearly for p-AKT, FOXO1, p65, and p52. Representative histograms of protein expression of p-AKT ( B ), FOXO1 ( C ), p65 ( D ), and p52 ( E ), and corresponding quantifications as MFI. ( F – I ) WT aILC2s were treated with FOXO1 inhibitor or vehicle. ( G and H ) Representative plots of GATA-3 ( G ) and Ki67 ( H ) expression levels and corresponding quantification (as MFI). ( I ) Cytokine levels in cell supernatant (per 10 3 ILC2s). ( J – M ) WT aILC2s were treated with FOXO1 activator or vehicle. ( K and L ) Representative plots of GATA-3 ( K ) and Ki67 ( L ) expression levels and corresponding quantification (as MFI). ( M ) Cytokine levels in cell supernatant (per 10 3 ILC2s). Data are presented as mean + SEM and are representative of at least 2 independent experiments. Statistical significance was assessed using 2-tailed Student’s t test; ** P < 0.01, *** P < 0.001, **** P < 0.0001.

    Article Snippet: When specified, 10 μg/mL VISTA agonist antibody (MH5A, BioLegend), 10 μg/mL VISTA antagonist antibody (13F3, Bio X Cell), 100 nM FOXO1 inhibitor (AS1842856, MedChemExpress), or 1 μM FOXO1 activator (LOM612, MedChemExpress) with corresponding isotype control or vehicle (DMSO) was further added to cultures for the indicated times.

    Techniques: Isolation, Staining, Expressing

    ( A – F ) Human peripheral ILC2s (hILC2s) were stimulated with or without rhIL-33 (100 ng/mL). ( B ) Representative plots of VISTA expression levels and corresponding quantification (as MFI). ( C – F ) hILC2s were treated with 5 μg/mL rhVSIG3 and vehicle control. ( C and D ) Representative plots of GATA-3 ( C ) and Ki67 ( D ) expression levels and corresponding quantification (as MFI). ( E ) Cytokine levels in hILC2 supernatant (per 10 3 ILC2s). ( F ) Representative plots of FOXO1 expression levels and corresponding quantification (as MFI) following 1 hour treatment with rhVSIG3. ( G – J ) A total of 2 × 10 5 hILC2s were transferred intravenously into Rag2 –/– GC –/– mice, followed by intranasal challenge with rhIL-33. On days 1 and 3, mice intravenously received 2 mg/kg rhVSIG3 or vehicle. ( H ) Lung resistance in response to elevating doses of methacholine. ( I ) Total number of ILC2s per lung. ( J ) Total number of eosinophils in BAL fluid. Data are presented as mean + SEM and are representative of at least 2 independent experiments. Statistical significance was assessed using either 2-tailed Student’s t test ( B – F , I , and J ) or 1-way ANOVA followed by Tukey’s post hoc test ( H ); * P < 0.05, ** P < 0.01.

    Journal: The Journal of Clinical Investigation

    Article Title: FOXO1 pathway activation by VISTA immune checkpoint restrains pulmonary ILC2 functions

    doi: 10.1172/JCI184932

    Figure Lengend Snippet: ( A – F ) Human peripheral ILC2s (hILC2s) were stimulated with or without rhIL-33 (100 ng/mL). ( B ) Representative plots of VISTA expression levels and corresponding quantification (as MFI). ( C – F ) hILC2s were treated with 5 μg/mL rhVSIG3 and vehicle control. ( C and D ) Representative plots of GATA-3 ( C ) and Ki67 ( D ) expression levels and corresponding quantification (as MFI). ( E ) Cytokine levels in hILC2 supernatant (per 10 3 ILC2s). ( F ) Representative plots of FOXO1 expression levels and corresponding quantification (as MFI) following 1 hour treatment with rhVSIG3. ( G – J ) A total of 2 × 10 5 hILC2s were transferred intravenously into Rag2 –/– GC –/– mice, followed by intranasal challenge with rhIL-33. On days 1 and 3, mice intravenously received 2 mg/kg rhVSIG3 or vehicle. ( H ) Lung resistance in response to elevating doses of methacholine. ( I ) Total number of ILC2s per lung. ( J ) Total number of eosinophils in BAL fluid. Data are presented as mean + SEM and are representative of at least 2 independent experiments. Statistical significance was assessed using either 2-tailed Student’s t test ( B – F , I , and J ) or 1-way ANOVA followed by Tukey’s post hoc test ( H ); * P < 0.05, ** P < 0.01.

    Article Snippet: When specified, 10 μg/mL VISTA agonist antibody (MH5A, BioLegend), 10 μg/mL VISTA antagonist antibody (13F3, Bio X Cell), 100 nM FOXO1 inhibitor (AS1842856, MedChemExpress), or 1 μM FOXO1 activator (LOM612, MedChemExpress) with corresponding isotype control or vehicle (DMSO) was further added to cultures for the indicated times.

    Techniques: Expressing, Control