il 21r Search Results


92
R&D Systems recombinant human il21r fc chimera
Recombinant Human Il21r Fc Chimera, supplied by R&D Systems, 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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93
R&D Systems recombinant mouse il 21 receptor fc
Recombinant Mouse Il 21 Receptor Fc, 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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91
R&D Systems anti mouse m il 21r
Anti Mouse M Il 21r, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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R&D Systems anti human il 21r
Anti Human Il 21r, 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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Average 93 stars, based on 1 article reviews
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94
R&D Systems recombinant mouse il 21r human fc chimera
( A ) Fecal pellets were collected from age-matched wild-type, IL-21 −/− , <t>and</t> <t>IL-21R</t> −/− B6 mice. IgA levels were quantified through ELISA and normalized to total protein. N = 2 mice per group, data is reflective of 2 independent experiments. *p<0.05 compared to wild-type mice. ( B ) Naïve IgD + B cells were activated with anti-µ (5µg/ml) and anti-CD40 (5µg/ml) in the presence of TGFβ1 (5ng/ml), IL-17 (50ng/ml), IL-21 (20ng/ml), or retinoic acid (1µM), or a combination of TGFβ1, IL-17, IL-21, and/or retinoic acid. On day 5, IgA was measured from the supernatant by ELISA. Data is reflective of 6 independent experiments. *p<0.05, ***p<0.001 compared between samples. + p<0.05, ++ p<0.01 compared to untreated cells.
Recombinant Mouse Il 21r Human Fc Chimera, 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
https://www.bioz.com/product/il+21r/Human+IL-21R+Antibody/pmc04501922-37-50-58
Average 94 stars, based on 1 article reviews
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92
R&D Systems allophycocyanin apc anti il 21r
( A ) Fecal pellets were collected from age-matched wild-type, IL-21 −/− , <t>and</t> <t>IL-21R</t> −/− B6 mice. IgA levels were quantified through ELISA and normalized to total protein. N = 2 mice per group, data is reflective of 2 independent experiments. *p<0.05 compared to wild-type mice. ( B ) Naïve IgD + B cells were activated with anti-µ (5µg/ml) and anti-CD40 (5µg/ml) in the presence of TGFβ1 (5ng/ml), IL-17 (50ng/ml), IL-21 (20ng/ml), or retinoic acid (1µM), or a combination of TGFβ1, IL-17, IL-21, and/or retinoic acid. On day 5, IgA was measured from the supernatant by ELISA. Data is reflective of 6 independent experiments. *p<0.05, ***p<0.001 compared between samples. + p<0.05, ++ p<0.01 compared to untreated cells.
Allophycocyanin Apc Anti Il 21r, supplied by R&D Systems, 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
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90
R&D Systems anti il 21r pe conjugated mab
( A ) Fecal pellets were collected from age-matched wild-type, IL-21 −/− , <t>and</t> <t>IL-21R</t> −/− B6 mice. IgA levels were quantified through ELISA and normalized to total protein. N = 2 mice per group, data is reflective of 2 independent experiments. *p<0.05 compared to wild-type mice. ( B ) Naïve IgD + B cells were activated with anti-µ (5µg/ml) and anti-CD40 (5µg/ml) in the presence of TGFβ1 (5ng/ml), IL-17 (50ng/ml), IL-21 (20ng/ml), or retinoic acid (1µM), or a combination of TGFβ1, IL-17, IL-21, and/or retinoic acid. On day 5, IgA was measured from the supernatant by ELISA. Data is reflective of 6 independent experiments. *p<0.05, ***p<0.001 compared between samples. + p<0.05, ++ p<0.01 compared to untreated cells.
Anti Il 21r Pe Conjugated 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/il+21r/Human+IL-21R+PE-conjugated+Antibody/pm16291655-55-0-5
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94
R&D Systems recombinant il 21r fc chimera protein
( A ) Fecal pellets were collected from age-matched wild-type, IL-21 −/− , <t>and</t> <t>IL-21R</t> −/− B6 mice. IgA levels were quantified through ELISA and normalized to total protein. N = 2 mice per group, data is reflective of 2 independent experiments. *p<0.05 compared to wild-type mice. ( B ) Naïve IgD + B cells were activated with anti-µ (5µg/ml) and anti-CD40 (5µg/ml) in the presence of TGFβ1 (5ng/ml), IL-17 (50ng/ml), IL-21 (20ng/ml), or retinoic acid (1µM), or a combination of TGFβ1, IL-17, IL-21, and/or retinoic acid. On day 5, IgA was measured from the supernatant by ELISA. Data is reflective of 6 independent experiments. *p<0.05, ***p<0.001 compared between samples. + p<0.05, ++ p<0.01 compared to untreated cells.
Recombinant Il 21r Fc Chimera Protein, 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
https://www.bioz.com/product/il+21r/Recombinant+Cynomolgus%2FRhesus+IL-21R+Fc+Chimera+Protein%2C+CF/pmc06824311-510-4-9
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93
Santa Cruz Biotechnology il 21r antibodies
( A ) Fecal pellets were collected from age-matched wild-type, IL-21 −/− , <t>and</t> <t>IL-21R</t> −/− B6 mice. IgA levels were quantified through ELISA and normalized to total protein. N = 2 mice per group, data is reflective of 2 independent experiments. *p<0.05 compared to wild-type mice. ( B ) Naïve IgD + B cells were activated with anti-µ (5µg/ml) and anti-CD40 (5µg/ml) in the presence of TGFβ1 (5ng/ml), IL-17 (50ng/ml), IL-21 (20ng/ml), or retinoic acid (1µM), or a combination of TGFβ1, IL-17, IL-21, and/or retinoic acid. On day 5, IgA was measured from the supernatant by ELISA. Data is reflective of 6 independent experiments. *p<0.05, ***p<0.001 compared between samples. + p<0.05, ++ p<0.01 compared to untreated cells.
Il 21r Antibodies, supplied by Santa Cruz Biotechnology, 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/product/il+21r/IL-21R+Antibody/pmc04496406-131-26-30
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85
R&D Systems goat anti human il 21r ab
( A ) Fecal pellets were collected from age-matched wild-type, IL-21 −/− , <t>and</t> <t>IL-21R</t> −/− B6 mice. IgA levels were quantified through ELISA and normalized to total protein. N = 2 mice per group, data is reflective of 2 independent experiments. *p<0.05 compared to wild-type mice. ( B ) Naïve IgD + B cells were activated with anti-µ (5µg/ml) and anti-CD40 (5µg/ml) in the presence of TGFβ1 (5ng/ml), IL-17 (50ng/ml), IL-21 (20ng/ml), or retinoic acid (1µM), or a combination of TGFβ1, IL-17, IL-21, and/or retinoic acid. On day 5, IgA was measured from the supernatant by ELISA. Data is reflective of 6 independent experiments. *p<0.05, ***p<0.001 compared between samples. + p<0.05, ++ p<0.01 compared to untreated cells.
Goat Anti Human Il 21r Ab, supplied by R&D Systems, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/il+21r/Human+IL-21R+Antibody/pm25780036-83-3-27
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93
R&D Systems recombinant mouse il 21r subunit
( A ) Fecal pellets were collected from age-matched wild-type, IL-21 −/− , <t>and</t> <t>IL-21R</t> −/− B6 mice. IgA levels were quantified through ELISA and normalized to total protein. N = 2 mice per group, data is reflective of 2 independent experiments. *p<0.05 compared to wild-type mice. ( B ) Naïve IgD + B cells were activated with anti-µ (5µg/ml) and anti-CD40 (5µg/ml) in the presence of TGFβ1 (5ng/ml), IL-17 (50ng/ml), IL-21 (20ng/ml), or retinoic acid (1µM), or a combination of TGFβ1, IL-17, IL-21, and/or retinoic acid. On day 5, IgA was measured from the supernatant by ELISA. Data is reflective of 6 independent experiments. *p<0.05, ***p<0.001 compared between samples. + p<0.05, ++ p<0.01 compared to untreated cells.
Recombinant Mouse Il 21r Subunit, 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
https://www.bioz.com/product/il+21r/Recombinant+Mouse+IL-21R+Fc+Chimera+Protein%2C+CF/pmc12494019-287-5-12
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90
R&D Systems goat anti mouse il 21r antibody
( A ) Fecal pellets were collected from age-matched wild-type, IL-21 −/− , <t>and</t> <t>IL-21R</t> −/− B6 mice. IgA levels were quantified through ELISA and normalized to total protein. N = 2 mice per group, data is reflective of 2 independent experiments. *p<0.05 compared to wild-type mice. ( B ) Naïve IgD + B cells were activated with anti-µ (5µg/ml) and anti-CD40 (5µg/ml) in the presence of TGFβ1 (5ng/ml), IL-17 (50ng/ml), IL-21 (20ng/ml), or retinoic acid (1µM), or a combination of TGFβ1, IL-17, IL-21, and/or retinoic acid. On day 5, IgA was measured from the supernatant by ELISA. Data is reflective of 6 independent experiments. *p<0.05, ***p<0.001 compared between samples. + p<0.05, ++ p<0.01 compared to untreated cells.
Goat Anti Mouse Il 21r Antibody, 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/il+21r/Mouse+IL-21R+Antibody/pelletier_martin__2006__effets_de_l_interleukine_15_et_de_l_interleukine_21_sur_les_neutrophiles-1050-6-18
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Image Search Results


( A ) Fecal pellets were collected from age-matched wild-type, IL-21 −/− , and IL-21R −/− B6 mice. IgA levels were quantified through ELISA and normalized to total protein. N = 2 mice per group, data is reflective of 2 independent experiments. *p<0.05 compared to wild-type mice. ( B ) Naïve IgD + B cells were activated with anti-µ (5µg/ml) and anti-CD40 (5µg/ml) in the presence of TGFβ1 (5ng/ml), IL-17 (50ng/ml), IL-21 (20ng/ml), or retinoic acid (1µM), or a combination of TGFβ1, IL-17, IL-21, and/or retinoic acid. On day 5, IgA was measured from the supernatant by ELISA. Data is reflective of 6 independent experiments. *p<0.05, ***p<0.001 compared between samples. + p<0.05, ++ p<0.01 compared to untreated cells.

Journal: Mucosal immunology

Article Title: Interleukin (IL)-21 promotes intestinal IgA response to microbiota

doi: 10.1038/mi.2014.134

Figure Lengend Snippet: ( A ) Fecal pellets were collected from age-matched wild-type, IL-21 −/− , and IL-21R −/− B6 mice. IgA levels were quantified through ELISA and normalized to total protein. N = 2 mice per group, data is reflective of 2 independent experiments. *p<0.05 compared to wild-type mice. ( B ) Naïve IgD + B cells were activated with anti-µ (5µg/ml) and anti-CD40 (5µg/ml) in the presence of TGFβ1 (5ng/ml), IL-17 (50ng/ml), IL-21 (20ng/ml), or retinoic acid (1µM), or a combination of TGFβ1, IL-17, IL-21, and/or retinoic acid. On day 5, IgA was measured from the supernatant by ELISA. Data is reflective of 6 independent experiments. *p<0.05, ***p<0.001 compared between samples. + p<0.05, ++ p<0.01 compared to untreated cells.

Article Snippet: The following antibodies were used for flow cytometry: PE-IL-17A (TC11-18H10.1), FITC-B220 (RA3-6B2), PE-α 4 β 7 (DATK32), FITC-CD4 (RM4-5), PE/Cy7-CD38 (90), APC-CD138 (281-2), and PE/Cy7-PD-1 (29F.1A12) were purchased from Biolegend; APC-RORγt (B2D), APC-GL-7, and eFluor450-Streptavidin were from eBioscience; Brilliant Violet 421-CD95 (Jo2) and biotinylated CXCR5 (2G8) were from BD Biosciences; recombinant mouse IL-21R human FC chimera was from R&D Systems; AlexaFluor 647 antihuman IgG FCγ (polyclonal) was from Jackson ImmunoResearch; PE-IgA (polyclonal) was from Southern Biotechnology.

Techniques: Enzyme-linked Immunosorbent Assay

10 6 CBir1 Th17 cells were i.v. transferred into TCR®x™ −/− mice. ( A ) On day 44 post-Th17 cell transfer, expression of surface IgA on splenic, intestinal lamina propria, or Peyer’s patch B cells of CBir1 Th17 cell recipients, Th17 cell recipients receiving neutralizing IL-21r (Th17+αIL-21r), or control TCRβxδ −/− mice was determined by flow cytometry. FACS plots are representative of 4 mice per group. ( B ) IgA + plasma cells and mature B cells in the spleens and intestines. Bar charts reflect mean +/− SEM. Data reflects 3 independent experiments. *p<0.05, **p<0.01, ***p<0.001 between compared samples. LPL = intestinal lamina propria lymphocytes; PP = Peyer’s patch; PC = plasma cell

Journal: Mucosal immunology

Article Title: Interleukin (IL)-21 promotes intestinal IgA response to microbiota

doi: 10.1038/mi.2014.134

Figure Lengend Snippet: 10 6 CBir1 Th17 cells were i.v. transferred into TCR®x™ −/− mice. ( A ) On day 44 post-Th17 cell transfer, expression of surface IgA on splenic, intestinal lamina propria, or Peyer’s patch B cells of CBir1 Th17 cell recipients, Th17 cell recipients receiving neutralizing IL-21r (Th17+αIL-21r), or control TCRβxδ −/− mice was determined by flow cytometry. FACS plots are representative of 4 mice per group. ( B ) IgA + plasma cells and mature B cells in the spleens and intestines. Bar charts reflect mean +/− SEM. Data reflects 3 independent experiments. *p<0.05, **p<0.01, ***p<0.001 between compared samples. LPL = intestinal lamina propria lymphocytes; PP = Peyer’s patch; PC = plasma cell

Article Snippet: The following antibodies were used for flow cytometry: PE-IL-17A (TC11-18H10.1), FITC-B220 (RA3-6B2), PE-α 4 β 7 (DATK32), FITC-CD4 (RM4-5), PE/Cy7-CD38 (90), APC-CD138 (281-2), and PE/Cy7-PD-1 (29F.1A12) were purchased from Biolegend; APC-RORγt (B2D), APC-GL-7, and eFluor450-Streptavidin were from eBioscience; Brilliant Violet 421-CD95 (Jo2) and biotinylated CXCR5 (2G8) were from BD Biosciences; recombinant mouse IL-21R human FC chimera was from R&D Systems; AlexaFluor 647 antihuman IgG FCγ (polyclonal) was from Jackson ImmunoResearch; PE-IgA (polyclonal) was from Southern Biotechnology.

Techniques: Expressing, Control, Flow Cytometry, Clinical Proteomics

( A ) On day 44 post-Th17 cell transfer, IgG and IgA in the serum was measured by ELISA. *p<0.05, **p<0.01, ***p<0.001 ( B ) Fecal pellets were collected from Th17 cell recipients during the course of the experiment. IgA levels were quantified through ELISA and normalized to total protein. Changes in expression over time are expressed as a fold change from individuals pre-transfer. N = 4 mice per group, from 3 independent experiments. *p<0.05 as compared to anti-IL-21r group. ( C ) Intracellular IgA production was measured from total bone marrow cells of CBir1 Th17 cell recipients, Th17 cell recipients receiving neutralizing IL-21r (Th17+αIL-21r), or control TCRβxδ −/− mice by flow cytometry. FACS plots are representative of 4 mice per group.

Journal: Mucosal immunology

Article Title: Interleukin (IL)-21 promotes intestinal IgA response to microbiota

doi: 10.1038/mi.2014.134

Figure Lengend Snippet: ( A ) On day 44 post-Th17 cell transfer, IgG and IgA in the serum was measured by ELISA. *p<0.05, **p<0.01, ***p<0.001 ( B ) Fecal pellets were collected from Th17 cell recipients during the course of the experiment. IgA levels were quantified through ELISA and normalized to total protein. Changes in expression over time are expressed as a fold change from individuals pre-transfer. N = 4 mice per group, from 3 independent experiments. *p<0.05 as compared to anti-IL-21r group. ( C ) Intracellular IgA production was measured from total bone marrow cells of CBir1 Th17 cell recipients, Th17 cell recipients receiving neutralizing IL-21r (Th17+αIL-21r), or control TCRβxδ −/− mice by flow cytometry. FACS plots are representative of 4 mice per group.

Article Snippet: The following antibodies were used for flow cytometry: PE-IL-17A (TC11-18H10.1), FITC-B220 (RA3-6B2), PE-α 4 β 7 (DATK32), FITC-CD4 (RM4-5), PE/Cy7-CD38 (90), APC-CD138 (281-2), and PE/Cy7-PD-1 (29F.1A12) were purchased from Biolegend; APC-RORγt (B2D), APC-GL-7, and eFluor450-Streptavidin were from eBioscience; Brilliant Violet 421-CD95 (Jo2) and biotinylated CXCR5 (2G8) were from BD Biosciences; recombinant mouse IL-21R human FC chimera was from R&D Systems; AlexaFluor 647 antihuman IgG FCγ (polyclonal) was from Jackson ImmunoResearch; PE-IgA (polyclonal) was from Southern Biotechnology.

Techniques: Enzyme-linked Immunosorbent Assay, Expressing, Control, Flow Cytometry

10 6 CBir1 Th17 cells were i.v. transferred into TCR®x™ −/− mice. ( A ) On day 44 post-Th17 cell transfer, expression of germinal center markers GL-7 and CD95 on splenic, mesenteric lymph node, intestinal lamina propria, or Peyer’s patch B220 + cells of CBir1 Th17 cell recipients, Th17 cell recipients receiving neutralizing IL-21r (Th17+αIL-21r), or control TCRβxδ −/− mice was determined by flow cytometry. FACS plots are representative of 4 mice per group. ( B ) IF image of Peyer’s patch from control TCRβxδ −/− mice or CBir1 Th17 cell recipients with 20× objective. Germinal center formation was analyzed by staining for GL-7-AlexaFluor 594 and B220-FITC. ( C ) RNA was collected from ileal tissue on day 44 post-Th17 cell transfer from CBir1 Th17 cell recipients or control TCRβxδ −/− mice and Aicda mRNA was analyzed by RT-PCR. Data is reflective of 4 mice per group, from 3 independent experiments.

Journal: Mucosal immunology

Article Title: Interleukin (IL)-21 promotes intestinal IgA response to microbiota

doi: 10.1038/mi.2014.134

Figure Lengend Snippet: 10 6 CBir1 Th17 cells were i.v. transferred into TCR®x™ −/− mice. ( A ) On day 44 post-Th17 cell transfer, expression of germinal center markers GL-7 and CD95 on splenic, mesenteric lymph node, intestinal lamina propria, or Peyer’s patch B220 + cells of CBir1 Th17 cell recipients, Th17 cell recipients receiving neutralizing IL-21r (Th17+αIL-21r), or control TCRβxδ −/− mice was determined by flow cytometry. FACS plots are representative of 4 mice per group. ( B ) IF image of Peyer’s patch from control TCRβxδ −/− mice or CBir1 Th17 cell recipients with 20× objective. Germinal center formation was analyzed by staining for GL-7-AlexaFluor 594 and B220-FITC. ( C ) RNA was collected from ileal tissue on day 44 post-Th17 cell transfer from CBir1 Th17 cell recipients or control TCRβxδ −/− mice and Aicda mRNA was analyzed by RT-PCR. Data is reflective of 4 mice per group, from 3 independent experiments.

Article Snippet: The following antibodies were used for flow cytometry: PE-IL-17A (TC11-18H10.1), FITC-B220 (RA3-6B2), PE-α 4 β 7 (DATK32), FITC-CD4 (RM4-5), PE/Cy7-CD38 (90), APC-CD138 (281-2), and PE/Cy7-PD-1 (29F.1A12) were purchased from Biolegend; APC-RORγt (B2D), APC-GL-7, and eFluor450-Streptavidin were from eBioscience; Brilliant Violet 421-CD95 (Jo2) and biotinylated CXCR5 (2G8) were from BD Biosciences; recombinant mouse IL-21R human FC chimera was from R&D Systems; AlexaFluor 647 antihuman IgG FCγ (polyclonal) was from Jackson ImmunoResearch; PE-IgA (polyclonal) was from Southern Biotechnology.

Techniques: Expressing, Control, Flow Cytometry, Staining, Reverse Transcription Polymerase Chain Reaction