µg mouse α il 33 Search Results


anti mouse il 33 antibody  (R&D Systems)
94
R&D Systems anti mouse il 33 antibody
Anti Mouse Il 33 Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
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µg mouse α il 17  (Bio-Techne corporation)
94
Bio-Techne corporation µg mouse α il 17
( A ) Female and male mice were infected with 10 7 CFU of UPEC strain UTI89-RFP-kan R and bladders analyzed by flow cytometry at 24 hours PI. Graphs show ( A ) the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and LTi-like cells (CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − ) in bladders. ( B ) Female mice were implanted with empty tubing (Mock) or slow release tubing containing testosterone (T tube) and allowed to recover 1 week before infection with 10 7 CFU UPEC strain UTI89-RFP-kan R . Graphs show the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − LTi-like cells in bladders. ( C-E ) Graphs show the number of infected mice, determined by urine sampling, over time in ( C ) wildtype or RAG2 − /-γc mice, ( D ) mice treated with isotype or αNK1.1-depleting antibody, ( E ) mice treated <t>with</t> <t>α-IL-17</t> neutralizing antibody. ( A-B ) Data are pooled from 2-3 experiments, n=4-5/group in each experiment. Each dot is one mouse, red dots depict female mice and blue dots are male mice, lines are medians. ( C-E ) Graphs are representative experiments, n=6-12 mice per experiment, at least 2 experiments each. * p<0.05, ** p<0.01, Mann-Whitney test. Analyses in this figure were corrected for multiple testing by Holm–Bonferroni method, all p<0.05 had q< 0.05.
µg Mouse α Il 17, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 94 stars, based on 1 article reviews
µg mouse α il 17 - by Bioz Stars, 2026-10
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recombinant mouse il 21r fc chimera  (Bio-Techne corporation)
94
Bio-Techne corporation recombinant mouse il 21r fc chimera
( A ) Female and male mice were infected with 10 7 CFU of UPEC strain UTI89-RFP-kan R and bladders analyzed by flow cytometry at 24 hours PI. Graphs show ( A ) the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and LTi-like cells (CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − ) in bladders. ( B ) Female mice were implanted with empty tubing (Mock) or slow release tubing containing testosterone (T tube) and allowed to recover 1 week before infection with 10 7 CFU UPEC strain UTI89-RFP-kan R . Graphs show the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − LTi-like cells in bladders. ( C-E ) Graphs show the number of infected mice, determined by urine sampling, over time in ( C ) wildtype or RAG2 − /-γc mice, ( D ) mice treated with isotype or αNK1.1-depleting antibody, ( E ) mice treated <t>with</t> <t>α-IL-17</t> neutralizing antibody. ( A-B ) Data are pooled from 2-3 experiments, n=4-5/group in each experiment. Each dot is one mouse, red dots depict female mice and blue dots are male mice, lines are medians. ( C-E ) Graphs are representative experiments, n=6-12 mice per experiment, at least 2 experiments each. * p<0.05, ** p<0.01, Mann-Whitney test. Analyses in this figure were corrected for multiple testing by Holm–Bonferroni method, all p<0.05 had q< 0.05.
Recombinant Mouse Il 21r Fc Chimera, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mouse anti-human il-4  (Becton Dickinson)
90
Becton Dickinson mouse anti-human il-4
( A ) Female and male mice were infected with 10 7 CFU of UPEC strain UTI89-RFP-kan R and bladders analyzed by flow cytometry at 24 hours PI. Graphs show ( A ) the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and LTi-like cells (CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − ) in bladders. ( B ) Female mice were implanted with empty tubing (Mock) or slow release tubing containing testosterone (T tube) and allowed to recover 1 week before infection with 10 7 CFU UPEC strain UTI89-RFP-kan R . Graphs show the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − LTi-like cells in bladders. ( C-E ) Graphs show the number of infected mice, determined by urine sampling, over time in ( C ) wildtype or RAG2 − /-γc mice, ( D ) mice treated with isotype or αNK1.1-depleting antibody, ( E ) mice treated <t>with</t> <t>α-IL-17</t> neutralizing antibody. ( A-B ) Data are pooled from 2-3 experiments, n=4-5/group in each experiment. Each dot is one mouse, red dots depict female mice and blue dots are male mice, lines are medians. ( C-E ) Graphs are representative experiments, n=6-12 mice per experiment, at least 2 experiments each. * p<0.05, ** p<0.01, Mann-Whitney test. Analyses in this figure were corrected for multiple testing by Holm–Bonferroni method, all p<0.05 had q< 0.05.
Mouse Anti Human Il 4, supplied by Becton Dickinson, 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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primary antibody anti mouse il 33  (R&D Systems)
97
R&D Systems primary antibody anti mouse il 33
( A ) Female and male mice were infected with 10 7 CFU of UPEC strain UTI89-RFP-kan R and bladders analyzed by flow cytometry at 24 hours PI. Graphs show ( A ) the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and LTi-like cells (CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − ) in bladders. ( B ) Female mice were implanted with empty tubing (Mock) or slow release tubing containing testosterone (T tube) and allowed to recover 1 week before infection with 10 7 CFU UPEC strain UTI89-RFP-kan R . Graphs show the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − LTi-like cells in bladders. ( C-E ) Graphs show the number of infected mice, determined by urine sampling, over time in ( C ) wildtype or RAG2 − /-γc mice, ( D ) mice treated with isotype or αNK1.1-depleting antibody, ( E ) mice treated <t>with</t> <t>α-IL-17</t> neutralizing antibody. ( A-B ) Data are pooled from 2-3 experiments, n=4-5/group in each experiment. Each dot is one mouse, red dots depict female mice and blue dots are male mice, lines are medians. ( C-E ) Graphs are representative experiments, n=6-12 mice per experiment, at least 2 experiments each. * p<0.05, ** p<0.01, Mann-Whitney test. Analyses in this figure were corrected for multiple testing by Holm–Bonferroni method, all p<0.05 had q< 0.05.
Primary Antibody Anti Mouse Il 33, supplied by R&D Systems, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 97 stars, based on 1 article reviews
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mouse il 33  (Elabscience Biotechnology)
94
Elabscience Biotechnology mouse il 33
( A ) Female and male mice were infected with 10 7 CFU of UPEC strain UTI89-RFP-kan R and bladders analyzed by flow cytometry at 24 hours PI. Graphs show ( A ) the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and LTi-like cells (CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − ) in bladders. ( B ) Female mice were implanted with empty tubing (Mock) or slow release tubing containing testosterone (T tube) and allowed to recover 1 week before infection with 10 7 CFU UPEC strain UTI89-RFP-kan R . Graphs show the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − LTi-like cells in bladders. ( C-E ) Graphs show the number of infected mice, determined by urine sampling, over time in ( C ) wildtype or RAG2 − /-γc mice, ( D ) mice treated with isotype or αNK1.1-depleting antibody, ( E ) mice treated <t>with</t> <t>α-IL-17</t> neutralizing antibody. ( A-B ) Data are pooled from 2-3 experiments, n=4-5/group in each experiment. Each dot is one mouse, red dots depict female mice and blue dots are male mice, lines are medians. ( C-E ) Graphs are representative experiments, n=6-12 mice per experiment, at least 2 experiments each. * p<0.05, ** p<0.01, Mann-Whitney test. Analyses in this figure were corrected for multiple testing by Holm–Bonferroni method, all p<0.05 had q< 0.05.
Mouse Il 33, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rat anti-mouse il-10  (Becton Dickinson)
90
Becton Dickinson rat anti-mouse il-10
( A ) Female and male mice were infected with 10 7 CFU of UPEC strain UTI89-RFP-kan R and bladders analyzed by flow cytometry at 24 hours PI. Graphs show ( A ) the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and LTi-like cells (CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − ) in bladders. ( B ) Female mice were implanted with empty tubing (Mock) or slow release tubing containing testosterone (T tube) and allowed to recover 1 week before infection with 10 7 CFU UPEC strain UTI89-RFP-kan R . Graphs show the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − LTi-like cells in bladders. ( C-E ) Graphs show the number of infected mice, determined by urine sampling, over time in ( C ) wildtype or RAG2 − /-γc mice, ( D ) mice treated with isotype or αNK1.1-depleting antibody, ( E ) mice treated <t>with</t> <t>α-IL-17</t> neutralizing antibody. ( A-B ) Data are pooled from 2-3 experiments, n=4-5/group in each experiment. Each dot is one mouse, red dots depict female mice and blue dots are male mice, lines are medians. ( C-E ) Graphs are representative experiments, n=6-12 mice per experiment, at least 2 experiments each. * p<0.05, ** p<0.01, Mann-Whitney test. Analyses in this figure were corrected for multiple testing by Holm–Bonferroni method, all p<0.05 had q< 0.05.
Rat Anti Mouse Il 10, supplied by Becton Dickinson, 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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mouse st2 il 33r duoset elisa kit  (R&D Systems)
93
R&D Systems mouse st2 il 33r duoset elisa kit
( A ) Female and male mice were infected with 10 7 CFU of UPEC strain UTI89-RFP-kan R and bladders analyzed by flow cytometry at 24 hours PI. Graphs show ( A ) the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and LTi-like cells (CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − ) in bladders. ( B ) Female mice were implanted with empty tubing (Mock) or slow release tubing containing testosterone (T tube) and allowed to recover 1 week before infection with 10 7 CFU UPEC strain UTI89-RFP-kan R . Graphs show the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − LTi-like cells in bladders. ( C-E ) Graphs show the number of infected mice, determined by urine sampling, over time in ( C ) wildtype or RAG2 − /-γc mice, ( D ) mice treated with isotype or αNK1.1-depleting antibody, ( E ) mice treated <t>with</t> <t>α-IL-17</t> neutralizing antibody. ( A-B ) Data are pooled from 2-3 experiments, n=4-5/group in each experiment. Each dot is one mouse, red dots depict female mice and blue dots are male mice, lines are medians. ( C-E ) Graphs are representative experiments, n=6-12 mice per experiment, at least 2 experiments each. * p<0.05, ** p<0.01, Mann-Whitney test. Analyses in this figure were corrected for multiple testing by Holm–Bonferroni method, all p<0.05 had q< 0.05.
Mouse St2 Il 33r Duoset Elisa Kit, supplied by R&D Systems, 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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mouse il-33 (interleukin 33) elisa kit  (Guangzhou JET Bio-Filtration)
94
Guangzhou JET Bio-Filtration mouse il-33 (interleukin 33) elisa kit
( A ) Female and male mice were infected with 10 7 CFU of UPEC strain UTI89-RFP-kan R and bladders analyzed by flow cytometry at 24 hours PI. Graphs show ( A ) the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and LTi-like cells (CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − ) in bladders. ( B ) Female mice were implanted with empty tubing (Mock) or slow release tubing containing testosterone (T tube) and allowed to recover 1 week before infection with 10 7 CFU UPEC strain UTI89-RFP-kan R . Graphs show the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − LTi-like cells in bladders. ( C-E ) Graphs show the number of infected mice, determined by urine sampling, over time in ( C ) wildtype or RAG2 − /-γc mice, ( D ) mice treated with isotype or αNK1.1-depleting antibody, ( E ) mice treated <t>with</t> <t>α-IL-17</t> neutralizing antibody. ( A-B ) Data are pooled from 2-3 experiments, n=4-5/group in each experiment. Each dot is one mouse, red dots depict female mice and blue dots are male mice, lines are medians. ( C-E ) Graphs are representative experiments, n=6-12 mice per experiment, at least 2 experiments each. * p<0.05, ** p<0.01, Mann-Whitney test. Analyses in this figure were corrected for multiple testing by Holm–Bonferroni method, all p<0.05 had q< 0.05.
Mouse Il 33 (Interleukin 33) Elisa Kit, supplied by Guangzhou JET Bio-Filtration, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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il 33 quantikine enzyme linked immunosorbent assay kit  (R&D Systems)
94
R&D Systems il 33 quantikine enzyme linked immunosorbent assay kit
( A ) Female and male mice were infected with 10 7 CFU of UPEC strain UTI89-RFP-kan R and bladders analyzed by flow cytometry at 24 hours PI. Graphs show ( A ) the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and LTi-like cells (CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − ) in bladders. ( B ) Female mice were implanted with empty tubing (Mock) or slow release tubing containing testosterone (T tube) and allowed to recover 1 week before infection with 10 7 CFU UPEC strain UTI89-RFP-kan R . Graphs show the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − LTi-like cells in bladders. ( C-E ) Graphs show the number of infected mice, determined by urine sampling, over time in ( C ) wildtype or RAG2 − /-γc mice, ( D ) mice treated with isotype or αNK1.1-depleting antibody, ( E ) mice treated <t>with</t> <t>α-IL-17</t> neutralizing antibody. ( A-B ) Data are pooled from 2-3 experiments, n=4-5/group in each experiment. Each dot is one mouse, red dots depict female mice and blue dots are male mice, lines are medians. ( C-E ) Graphs are representative experiments, n=6-12 mice per experiment, at least 2 experiments each. * p<0.05, ** p<0.01, Mann-Whitney test. Analyses in this figure were corrected for multiple testing by Holm–Bonferroni method, all p<0.05 had q< 0.05.
Il 33 Quantikine Enzyme Linked Immunosorbent Assay Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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mouse duoset il 33 elisa  (R&D Systems)
95
R&D Systems mouse duoset il 33 elisa
( A ) Female and male mice were infected with 10 7 CFU of UPEC strain UTI89-RFP-kan R and bladders analyzed by flow cytometry at 24 hours PI. Graphs show ( A ) the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and LTi-like cells (CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − ) in bladders. ( B ) Female mice were implanted with empty tubing (Mock) or slow release tubing containing testosterone (T tube) and allowed to recover 1 week before infection with 10 7 CFU UPEC strain UTI89-RFP-kan R . Graphs show the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − LTi-like cells in bladders. ( C-E ) Graphs show the number of infected mice, determined by urine sampling, over time in ( C ) wildtype or RAG2 − /-γc mice, ( D ) mice treated with isotype or αNK1.1-depleting antibody, ( E ) mice treated <t>with</t> <t>α-IL-17</t> neutralizing antibody. ( A-B ) Data are pooled from 2-3 experiments, n=4-5/group in each experiment. Each dot is one mouse, red dots depict female mice and blue dots are male mice, lines are medians. ( C-E ) Graphs are representative experiments, n=6-12 mice per experiment, at least 2 experiments each. * p<0.05, ** p<0.01, Mann-Whitney test. Analyses in this figure were corrected for multiple testing by Holm–Bonferroni method, all p<0.05 had q< 0.05.
Mouse Duoset Il 33 Elisa, supplied by R&D Systems, 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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recombinant mouse il-33 protein  (Bio-Techne corporation)
95
Bio-Techne corporation recombinant mouse il-33 protein
( A ) Female and male mice were infected with 10 7 CFU of UPEC strain UTI89-RFP-kan R and bladders analyzed by flow cytometry at 24 hours PI. Graphs show ( A ) the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and LTi-like cells (CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − ) in bladders. ( B ) Female mice were implanted with empty tubing (Mock) or slow release tubing containing testosterone (T tube) and allowed to recover 1 week before infection with 10 7 CFU UPEC strain UTI89-RFP-kan R . Graphs show the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − LTi-like cells in bladders. ( C-E ) Graphs show the number of infected mice, determined by urine sampling, over time in ( C ) wildtype or RAG2 − /-γc mice, ( D ) mice treated with isotype or αNK1.1-depleting antibody, ( E ) mice treated <t>with</t> <t>α-IL-17</t> neutralizing antibody. ( A-B ) Data are pooled from 2-3 experiments, n=4-5/group in each experiment. Each dot is one mouse, red dots depict female mice and blue dots are male mice, lines are medians. ( C-E ) Graphs are representative experiments, n=6-12 mice per experiment, at least 2 experiments each. * p<0.05, ** p<0.01, Mann-Whitney test. Analyses in this figure were corrected for multiple testing by Holm–Bonferroni method, all p<0.05 had q< 0.05.
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Image Search Results


( A ) Female and male mice were infected with 10 7 CFU of UPEC strain UTI89-RFP-kan R and bladders analyzed by flow cytometry at 24 hours PI. Graphs show ( A ) the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and LTi-like cells (CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − ) in bladders. ( B ) Female mice were implanted with empty tubing (Mock) or slow release tubing containing testosterone (T tube) and allowed to recover 1 week before infection with 10 7 CFU UPEC strain UTI89-RFP-kan R . Graphs show the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − LTi-like cells in bladders. ( C-E ) Graphs show the number of infected mice, determined by urine sampling, over time in ( C ) wildtype or RAG2 − /-γc mice, ( D ) mice treated with isotype or αNK1.1-depleting antibody, ( E ) mice treated with α-IL-17 neutralizing antibody. ( A-B ) Data are pooled from 2-3 experiments, n=4-5/group in each experiment. Each dot is one mouse, red dots depict female mice and blue dots are male mice, lines are medians. ( C-E ) Graphs are representative experiments, n=6-12 mice per experiment, at least 2 experiments each. * p<0.05, ** p<0.01, Mann-Whitney test. Analyses in this figure were corrected for multiple testing by Holm–Bonferroni method, all p<0.05 had q< 0.05.

Journal: bioRxiv

Article Title: Sex differences in IL-17 determine chronicity in male versus female urinary tract infection

doi: 10.1101/449124

Figure Lengend Snippet: ( A ) Female and male mice were infected with 10 7 CFU of UPEC strain UTI89-RFP-kan R and bladders analyzed by flow cytometry at 24 hours PI. Graphs show ( A ) the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and LTi-like cells (CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − ) in bladders. ( B ) Female mice were implanted with empty tubing (Mock) or slow release tubing containing testosterone (T tube) and allowed to recover 1 week before infection with 10 7 CFU UPEC strain UTI89-RFP-kan R . Graphs show the number of CD3 + CD4 + T cells, CD3 − NK1.1 + NK cells, γδ T cells, and CD90 + CD25 + CD4 + CD3 − NK1.1 − MHC II − CD11b − LTi-like cells in bladders. ( C-E ) Graphs show the number of infected mice, determined by urine sampling, over time in ( C ) wildtype or RAG2 − /-γc mice, ( D ) mice treated with isotype or αNK1.1-depleting antibody, ( E ) mice treated with α-IL-17 neutralizing antibody. ( A-B ) Data are pooled from 2-3 experiments, n=4-5/group in each experiment. Each dot is one mouse, red dots depict female mice and blue dots are male mice, lines are medians. ( C-E ) Graphs are representative experiments, n=6-12 mice per experiment, at least 2 experiments each. * p<0.05, ** p<0.01, Mann-Whitney test. Analyses in this figure were corrected for multiple testing by Holm–Bonferroni method, all p<0.05 had q< 0.05.

Article Snippet: For IL-17 neutralization, 83.3-111 µg/mouse α-IL-17 (clone 50104, BioTechne/R&D Systems) or 83.3-111 µg/mouse rat IgG2a isotype control (clone 54447, BioXcell) were delivered intravenously in 100 µL PBS.

Techniques: Infection, Flow Cytometry, Sampling, MANN-WHITNEY