chicken ova323 339 peptide Search Results


96
InvivoGen ova 257 264 peptide
Identification of astemizole and ikarugamycin as immunostimulatory agents. (A–D) De-ini dendritic cells (DC) were cultured with the compounds of the indicated chemical libraries for 16 hours, then washed twice and pulsed with 500 µg/mL ovalbumin <t>(OVA)</t> protein for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells for 16 hours. Then, the supernatant of cells was harvested and the production of interleukin 2 (IL2), as an indicator for antigen cross-presentation capacity, was measured by ELISA. IL2 concentration was normalized according to dimethyl sulfoxide (DMSO)-treated controls. (E–F) De-iniDCs and bone marrow-derived DCs (BMDCs) were treated with DMSO or ikarugamycin (0.1, 0.2, 0.5, 1 µM) (E), or astemizole (0.2, 0.5, 1, 2, 5 µM) (F) for 16 hours, then washed twice and pulsed with OVA protein or 10 ng/mL OVA257-264 peptide <t>(SL8,</t> as a positive control) for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells. IL-2 secretion was measured by ELISA as an indication for antigen cross-presentation capacity. Data are reported as the mean±SD of three replicates, and statistical analyses were performed with a two-tailed unpaired Student’s t test. de-iniDCs, de-induced/de-immortalized DCs.
Ova 257 264 Peptide, supplied by InvivoGen, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biosynth Carbosynth chicken ova323 339 peptide
Identification of astemizole and ikarugamycin as immunostimulatory agents. (A–D) De-ini dendritic cells (DC) were cultured with the compounds of the indicated chemical libraries for 16 hours, then washed twice and pulsed with 500 µg/mL ovalbumin <t>(OVA)</t> protein for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells for 16 hours. Then, the supernatant of cells was harvested and the production of interleukin 2 (IL2), as an indicator for antigen cross-presentation capacity, was measured by ELISA. IL2 concentration was normalized according to dimethyl sulfoxide (DMSO)-treated controls. (E–F) De-iniDCs and bone marrow-derived DCs (BMDCs) were treated with DMSO or ikarugamycin (0.1, 0.2, 0.5, 1 µM) (E), or astemizole (0.2, 0.5, 1, 2, 5 µM) (F) for 16 hours, then washed twice and pulsed with OVA protein or 10 ng/mL OVA257-264 peptide <t>(SL8,</t> as a positive control) for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells. IL-2 secretion was measured by ELISA as an indication for antigen cross-presentation capacity. Data are reported as the mean±SD of three replicates, and statistical analyses were performed with a two-tailed unpaired Student’s t test. de-iniDCs, de-induced/de-immortalized DCs.
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90
AnaSpec mouse mog 35–55 peptide
Identification of astemizole and ikarugamycin as immunostimulatory agents. (A–D) De-ini dendritic cells (DC) were cultured with the compounds of the indicated chemical libraries for 16 hours, then washed twice and pulsed with 500 µg/mL ovalbumin <t>(OVA)</t> protein for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells for 16 hours. Then, the supernatant of cells was harvested and the production of interleukin 2 (IL2), as an indicator for antigen cross-presentation capacity, was measured by ELISA. IL2 concentration was normalized according to dimethyl sulfoxide (DMSO)-treated controls. (E–F) De-iniDCs and bone marrow-derived DCs (BMDCs) were treated with DMSO or ikarugamycin (0.1, 0.2, 0.5, 1 µM) (E), or astemizole (0.2, 0.5, 1, 2, 5 µM) (F) for 16 hours, then washed twice and pulsed with OVA protein or 10 ng/mL OVA257-264 peptide <t>(SL8,</t> as a positive control) for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells. IL-2 secretion was measured by ELISA as an indication for antigen cross-presentation capacity. Data are reported as the mean±SD of three replicates, and statistical analyses were performed with a two-tailed unpaired Student’s t test. de-iniDCs, de-induced/de-immortalized DCs.
Mouse Mog 35–55 Peptide, supplied by AnaSpec, 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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90
GenScript corporation antigenic peptide ova 323–339
Identification of astemizole and ikarugamycin as immunostimulatory agents. (A–D) De-ini dendritic cells (DC) were cultured with the compounds of the indicated chemical libraries for 16 hours, then washed twice and pulsed with 500 µg/mL ovalbumin <t>(OVA)</t> protein for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells for 16 hours. Then, the supernatant of cells was harvested and the production of interleukin 2 (IL2), as an indicator for antigen cross-presentation capacity, was measured by ELISA. IL2 concentration was normalized according to dimethyl sulfoxide (DMSO)-treated controls. (E–F) De-iniDCs and bone marrow-derived DCs (BMDCs) were treated with DMSO or ikarugamycin (0.1, 0.2, 0.5, 1 µM) (E), or astemizole (0.2, 0.5, 1, 2, 5 µM) (F) for 16 hours, then washed twice and pulsed with OVA protein or 10 ng/mL OVA257-264 peptide <t>(SL8,</t> as a positive control) for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells. IL-2 secretion was measured by ELISA as an indication for antigen cross-presentation capacity. Data are reported as the mean±SD of three replicates, and statistical analyses were performed with a two-tailed unpaired Student’s t test. de-iniDCs, de-induced/de-immortalized DCs.
Antigenic Peptide Ova 323–339, supplied by GenScript corporation, 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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90
Peptron Inc chicken ova323–339 (isqavhaahaeineagr)
Identification of astemizole and ikarugamycin as immunostimulatory agents. (A–D) De-ini dendritic cells (DC) were cultured with the compounds of the indicated chemical libraries for 16 hours, then washed twice and pulsed with 500 µg/mL ovalbumin <t>(OVA)</t> protein for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells for 16 hours. Then, the supernatant of cells was harvested and the production of interleukin 2 (IL2), as an indicator for antigen cross-presentation capacity, was measured by ELISA. IL2 concentration was normalized according to dimethyl sulfoxide (DMSO)-treated controls. (E–F) De-iniDCs and bone marrow-derived DCs (BMDCs) were treated with DMSO or ikarugamycin (0.1, 0.2, 0.5, 1 µM) (E), or astemizole (0.2, 0.5, 1, 2, 5 µM) (F) for 16 hours, then washed twice and pulsed with OVA protein or 10 ng/mL OVA257-264 peptide <t>(SL8,</t> as a positive control) for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells. IL-2 secretion was measured by ELISA as an indication for antigen cross-presentation capacity. Data are reported as the mean±SD of three replicates, and statistical analyses were performed with a two-tailed unpaired Student’s t test. de-iniDCs, de-induced/de-immortalized DCs.
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90
Neo MPS Inc chicken ova peptide ova 323–339
Identification of astemizole and ikarugamycin as immunostimulatory agents. (A–D) De-ini dendritic cells (DC) were cultured with the compounds of the indicated chemical libraries for 16 hours, then washed twice and pulsed with 500 µg/mL ovalbumin <t>(OVA)</t> protein for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells for 16 hours. Then, the supernatant of cells was harvested and the production of interleukin 2 (IL2), as an indicator for antigen cross-presentation capacity, was measured by ELISA. IL2 concentration was normalized according to dimethyl sulfoxide (DMSO)-treated controls. (E–F) De-iniDCs and bone marrow-derived DCs (BMDCs) were treated with DMSO or ikarugamycin (0.1, 0.2, 0.5, 1 µM) (E), or astemizole (0.2, 0.5, 1, 2, 5 µM) (F) for 16 hours, then washed twice and pulsed with OVA protein or 10 ng/mL OVA257-264 peptide <t>(SL8,</t> as a positive control) for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells. IL-2 secretion was measured by ELISA as an indication for antigen cross-presentation capacity. Data are reported as the mean±SD of three replicates, and statistical analyses were performed with a two-tailed unpaired Student’s t test. de-iniDCs, de-induced/de-immortalized DCs.
Chicken Ova Peptide Ova 323–339, supplied by Neo MPS Inc, 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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94
Biosynth Carbosynth ova 323 339 isqavhaahaeineagr
Identification of astemizole and ikarugamycin as immunostimulatory agents. (A–D) De-ini dendritic cells (DC) were cultured with the compounds of the indicated chemical libraries for 16 hours, then washed twice and pulsed with 500 µg/mL ovalbumin <t>(OVA)</t> protein for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells for 16 hours. Then, the supernatant of cells was harvested and the production of interleukin 2 (IL2), as an indicator for antigen cross-presentation capacity, was measured by ELISA. IL2 concentration was normalized according to dimethyl sulfoxide (DMSO)-treated controls. (E–F) De-iniDCs and bone marrow-derived DCs (BMDCs) were treated with DMSO or ikarugamycin (0.1, 0.2, 0.5, 1 µM) (E), or astemizole (0.2, 0.5, 1, 2, 5 µM) (F) for 16 hours, then washed twice and pulsed with OVA protein or 10 ng/mL OVA257-264 peptide <t>(SL8,</t> as a positive control) for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells. IL-2 secretion was measured by ELISA as an indication for antigen cross-presentation capacity. Data are reported as the mean±SD of three replicates, and statistical analyses were performed with a two-tailed unpaired Student’s t test. de-iniDCs, de-induced/de-immortalized DCs.
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90
LifeTein Inc chicken ova (323-339)
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Jackson Laboratory ot-ii transgenic mice
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Ot Ii Transgenic Mice, supplied by Jackson Laboratory, 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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GenScript corporation chicken ova 323–339 peptide
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Chicken Ova 323–339 Peptide, supplied by GenScript corporation, 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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Alpha Diagnostics rabbit anti-chicken ova(323-339) igg
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Millipore chicken ova323-339 peptide
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Image Search Results


Identification of astemizole and ikarugamycin as immunostimulatory agents. (A–D) De-ini dendritic cells (DC) were cultured with the compounds of the indicated chemical libraries for 16 hours, then washed twice and pulsed with 500 µg/mL ovalbumin (OVA) protein for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells for 16 hours. Then, the supernatant of cells was harvested and the production of interleukin 2 (IL2), as an indicator for antigen cross-presentation capacity, was measured by ELISA. IL2 concentration was normalized according to dimethyl sulfoxide (DMSO)-treated controls. (E–F) De-iniDCs and bone marrow-derived DCs (BMDCs) were treated with DMSO or ikarugamycin (0.1, 0.2, 0.5, 1 µM) (E), or astemizole (0.2, 0.5, 1, 2, 5 µM) (F) for 16 hours, then washed twice and pulsed with OVA protein or 10 ng/mL OVA257-264 peptide (SL8, as a positive control) for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells. IL-2 secretion was measured by ELISA as an indication for antigen cross-presentation capacity. Data are reported as the mean±SD of three replicates, and statistical analyses were performed with a two-tailed unpaired Student’s t test. de-iniDCs, de-induced/de-immortalized DCs.

Journal: Journal for Immunotherapy of Cancer

Article Title: Anticancer effects of ikarugamycin and astemizole identified in a screen for stimulators of cellular immune responses

doi: 10.1136/jitc-2023-006785

Figure Lengend Snippet: Identification of astemizole and ikarugamycin as immunostimulatory agents. (A–D) De-ini dendritic cells (DC) were cultured with the compounds of the indicated chemical libraries for 16 hours, then washed twice and pulsed with 500 µg/mL ovalbumin (OVA) protein for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells for 16 hours. Then, the supernatant of cells was harvested and the production of interleukin 2 (IL2), as an indicator for antigen cross-presentation capacity, was measured by ELISA. IL2 concentration was normalized according to dimethyl sulfoxide (DMSO)-treated controls. (E–F) De-iniDCs and bone marrow-derived DCs (BMDCs) were treated with DMSO or ikarugamycin (0.1, 0.2, 0.5, 1 µM) (E), or astemizole (0.2, 0.5, 1, 2, 5 µM) (F) for 16 hours, then washed twice and pulsed with OVA protein or 10 ng/mL OVA257-264 peptide (SL8, as a positive control) for 4 hours, washed again twice, and then co-cultured with B3Z hybridoma cells. IL-2 secretion was measured by ELISA as an indication for antigen cross-presentation capacity. Data are reported as the mean±SD of three replicates, and statistical analyses were performed with a two-tailed unpaired Student’s t test. de-iniDCs, de-induced/de-immortalized DCs.

Article Snippet: OVA 257–264 peptide (SL8, Cat# vac-sin) was obtained from Invivogen (San Diego, California, USA).

Techniques: Cell Culture, Enzyme-linked Immunosorbent Assay, Concentration Assay, Derivative Assay, Positive Control, Two Tailed Test

KEY RESOURCES TABLE

Journal: Cell reports

Article Title: T Cell-Intrinsic IRF5 Regulates T Cell Signaling, Migration, and Differentiation and Promotes Intestinal Inflammation

doi: 10.1016/j.celrep.2020.107820

Figure Lengend Snippet: KEY RESOURCES TABLE

Article Snippet: Chicken OVA (323-339) , Lifetein , Cat# LT51023.

Techniques: Enzyme-linked Immunosorbent Assay, Recombinant, Sonication, DNA Library Preparation, Purification, Activation Assay, cDNA Synthesis, Software