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ppe anti il 7rα  (Bio X Cell)


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    Structured Review

    Bio X Cell ppe anti il 7rα
    Ppe Anti Il 7rα, supplied by Bio X Cell, used in various techniques. Bioz Stars score: 93/100, based on 64 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/ppe anti il 7rα/product/Bio X Cell
    Average 93 stars, based on 64 article reviews
    ppe anti il 7rα - by Bioz Stars, 2026-06
    93/100 stars

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    Bio X Cell anti il 7rα antibody
    a Flow cytometric analysis of fetal lungs from asthmatic or control mothers (day 18 of fetal life); ILC2s were stimulated with PMA/ionomycin for 4 h, and cytokine production was assessed by intracellular staining. b Model of maternal <t>anti-IL-7Rα</t> treatment in late pregnancy. Female mice developed asthma during pregnancy (Fig. ) and were treated intravenously with isotype or anti-IL-7Rα antibodies on days 14, 16, and 18 of gestation. c Adult offspring of antibody-treated asthmatic mothers received PBS or HDM intranasally (Fig. ). Changes in eosinophil and ILC2 cell numbers in the lungs of adult offspring; ILC2s were stimulated with PMA/ionomycin for 4 h, and cytokine production was assessed by intracellular staining. In ( a , c ), data are representative of two independent experiments [( a ), intracellular staining was evaluated once], each experiment with one pregnant dam per group, or pooled from two independent experiments, each experiment with one or two pregnant dams. Sample sizes were as follows: a PBS: n = 7, OVA: n = 6; c OVA(Iso)-PBS: n = 9, OVA(anti-IL-7Rα)-PBS: n = 6, OVA(Iso)-HDM: n = 14, OVA(anti-IL-7Rα)-HDM: n = 8. In ( a , c ), each dot represents an individual mouse. In ( a , c ), data are presented as the mean ± SEM. * p < 0.05; **** p < 0.0001; ns, not significant [unpaired two-tailed Student’s t -test].
    Anti Il 7rα Antibody, supplied by Bio X Cell, 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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    Fig. 3 | Pulmonary immune changes in embryonic life affect adult allergic responses. a Flow cytometric analysis of fetal lungs from asthmatic or control mothers (day 18 of fetal life); ILC2s were stimulated with PMA/ionomycin for 4 h, and cytokine production was assessed by intracellular staining. b Model of maternal <t>anti-IL-7Rα</t> treatment in late pregnancy. Female mice developed asthma during pregnancy (Fig. 1a) and were treated intravenously with isotype or anti-IL- 7Rα antibodies on days 14, 16, and 18 of gestation. c Adult offspring of antibody- treated asthmatic mothers received PBS or HDM intranasally (Fig. 1a). Changes in eosinophil and ILC2 cell numbers in the lungs of adult offspring; ILC2s were
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    Fig. 3 | Pulmonary immune changes in embryonic life affect adult allergic responses. a Flow cytometric analysis of fetal lungs from asthmatic or control mothers (day 18 of fetal life); ILC2s were stimulated with PMA/ionomycin for 4 h, and cytokine production was assessed by intracellular staining. b Model of maternal <t>anti-IL-7Rα</t> treatment in late pregnancy. Female mice developed asthma during pregnancy (Fig. 1a) and were treated intravenously with isotype or anti-IL- 7Rα antibodies on days 14, 16, and 18 of gestation. c Adult offspring of antibody- treated asthmatic mothers received PBS or HDM intranasally (Fig. 1a). Changes in eosinophil and ILC2 cell numbers in the lungs of adult offspring; ILC2s were
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    Fig. 3 | Pulmonary immune changes in embryonic life affect adult allergic responses. a Flow cytometric analysis of fetal lungs from asthmatic or control mothers (day 18 of fetal life); ILC2s were stimulated with PMA/ionomycin for 4 h, and cytokine production was assessed by intracellular staining. b Model of maternal <t>anti-IL-7Rα</t> treatment in late pregnancy. Female mice developed asthma during pregnancy (Fig. 1a) and were treated intravenously with isotype or anti-IL- 7Rα antibodies on days 14, 16, and 18 of gestation. c Adult offspring of antibody- treated asthmatic mothers received PBS or HDM intranasally (Fig. 1a). Changes in eosinophil and ILC2 cell numbers in the lungs of adult offspring; ILC2s were
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    Fig. 3 | Pulmonary immune changes in embryonic life affect adult allergic responses. a Flow cytometric analysis of fetal lungs from asthmatic or control mothers (day 18 of fetal life); ILC2s were stimulated with PMA/ionomycin for 4 h, and cytokine production was assessed by intracellular staining. b Model of maternal <t>anti-IL-7Rα</t> treatment in late pregnancy. Female mice developed asthma during pregnancy (Fig. 1a) and were treated intravenously with isotype or anti-IL- 7Rα antibodies on days 14, 16, and 18 of gestation. c Adult offspring of antibody- treated asthmatic mothers received PBS or HDM intranasally (Fig. 1a). Changes in eosinophil and ILC2 cell numbers in the lungs of adult offspring; ILC2s were
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    Bio X Cell be0089
    Fig. 3 | Pulmonary immune changes in embryonic life affect adult allergic responses. a Flow cytometric analysis of fetal lungs from asthmatic or control mothers (day 18 of fetal life); ILC2s were stimulated with PMA/ionomycin for 4 h, and cytokine production was assessed by intracellular staining. b Model of maternal <t>anti-IL-7Rα</t> treatment in late pregnancy. Female mice developed asthma during pregnancy (Fig. 1a) and were treated intravenously with isotype or anti-IL- 7Rα antibodies on days 14, 16, and 18 of gestation. c Adult offspring of antibody- treated asthmatic mothers received PBS or HDM intranasally (Fig. 1a). Changes in eosinophil and ILC2 cell numbers in the lungs of adult offspring; ILC2s were
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    a Flow cytometric analysis of fetal lungs from asthmatic or control mothers (day 18 of fetal life); ILC2s were stimulated with PMA/ionomycin for 4 h, and cytokine production was assessed by intracellular staining. b Model of maternal anti-IL-7Rα treatment in late pregnancy. Female mice developed asthma during pregnancy (Fig. ) and were treated intravenously with isotype or anti-IL-7Rα antibodies on days 14, 16, and 18 of gestation. c Adult offspring of antibody-treated asthmatic mothers received PBS or HDM intranasally (Fig. ). Changes in eosinophil and ILC2 cell numbers in the lungs of adult offspring; ILC2s were stimulated with PMA/ionomycin for 4 h, and cytokine production was assessed by intracellular staining. In ( a , c ), data are representative of two independent experiments [( a ), intracellular staining was evaluated once], each experiment with one pregnant dam per group, or pooled from two independent experiments, each experiment with one or two pregnant dams. Sample sizes were as follows: a PBS: n = 7, OVA: n = 6; c OVA(Iso)-PBS: n = 9, OVA(anti-IL-7Rα)-PBS: n = 6, OVA(Iso)-HDM: n = 14, OVA(anti-IL-7Rα)-HDM: n = 8. In ( a , c ), each dot represents an individual mouse. In ( a , c ), data are presented as the mean ± SEM. * p < 0.05; **** p < 0.0001; ns, not significant [unpaired two-tailed Student’s t -test].

    Journal: Nature Communications

    Article Title: Maternal asthma imprints fetal lung ILC2s via glucocorticoid signaling leading to worsened allergic airway inflammation in murine adult offspring

    doi: 10.1038/s41467-025-55941-8

    Figure Lengend Snippet: a Flow cytometric analysis of fetal lungs from asthmatic or control mothers (day 18 of fetal life); ILC2s were stimulated with PMA/ionomycin for 4 h, and cytokine production was assessed by intracellular staining. b Model of maternal anti-IL-7Rα treatment in late pregnancy. Female mice developed asthma during pregnancy (Fig. ) and were treated intravenously with isotype or anti-IL-7Rα antibodies on days 14, 16, and 18 of gestation. c Adult offspring of antibody-treated asthmatic mothers received PBS or HDM intranasally (Fig. ). Changes in eosinophil and ILC2 cell numbers in the lungs of adult offspring; ILC2s were stimulated with PMA/ionomycin for 4 h, and cytokine production was assessed by intracellular staining. In ( a , c ), data are representative of two independent experiments [( a ), intracellular staining was evaluated once], each experiment with one pregnant dam per group, or pooled from two independent experiments, each experiment with one or two pregnant dams. Sample sizes were as follows: a PBS: n = 7, OVA: n = 6; c OVA(Iso)-PBS: n = 9, OVA(anti-IL-7Rα)-PBS: n = 6, OVA(Iso)-HDM: n = 14, OVA(anti-IL-7Rα)-HDM: n = 8. In ( a , c ), each dot represents an individual mouse. In ( a , c ), data are presented as the mean ± SEM. * p < 0.05; **** p < 0.0001; ns, not significant [unpaired two-tailed Student’s t -test].

    Article Snippet: For depletion of fetal ILC2, IL-7Ra blockade was performed by intravenous injection of 200 μg isotype control (Bio X Cell, BE0089) or anti-IL-7Rα antibody (Bio X Cell, BE0065) into pregnant female mice on days 14, 16, and 18 of gestation.

    Techniques: Control, Staining, Two Tailed Test

    Fig. 3 | Pulmonary immune changes in embryonic life affect adult allergic responses. a Flow cytometric analysis of fetal lungs from asthmatic or control mothers (day 18 of fetal life); ILC2s were stimulated with PMA/ionomycin for 4 h, and cytokine production was assessed by intracellular staining. b Model of maternal anti-IL-7Rα treatment in late pregnancy. Female mice developed asthma during pregnancy (Fig. 1a) and were treated intravenously with isotype or anti-IL- 7Rα antibodies on days 14, 16, and 18 of gestation. c Adult offspring of antibody- treated asthmatic mothers received PBS or HDM intranasally (Fig. 1a). Changes in eosinophil and ILC2 cell numbers in the lungs of adult offspring; ILC2s were

    Journal: Nature communications

    Article Title: Maternal asthma imprints fetal lung ILC2s via glucocorticoid signaling leading to worsened allergic airway inflammation in murine adult offspring.

    doi: 10.1038/s41467-025-55941-8

    Figure Lengend Snippet: Fig. 3 | Pulmonary immune changes in embryonic life affect adult allergic responses. a Flow cytometric analysis of fetal lungs from asthmatic or control mothers (day 18 of fetal life); ILC2s were stimulated with PMA/ionomycin for 4 h, and cytokine production was assessed by intracellular staining. b Model of maternal anti-IL-7Rα treatment in late pregnancy. Female mice developed asthma during pregnancy (Fig. 1a) and were treated intravenously with isotype or anti-IL- 7Rα antibodies on days 14, 16, and 18 of gestation. c Adult offspring of antibody- treated asthmatic mothers received PBS or HDM intranasally (Fig. 1a). Changes in eosinophil and ILC2 cell numbers in the lungs of adult offspring; ILC2s were

    Article Snippet: For depletion of fetal ILC2, IL-7Ra blockade was performed by intravenous injection of 200 μg isotype control (BioXCell, BE0089) or antiIL-7Rα antibody (Bio X Cell, BE0065) into pregnant female mice on days 14, 16, and 18 of gestation.

    Techniques: Control, Staining