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Becton Dickinson set a9
Set A9, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/set a9/product/Becton Dickinson
Average 86 stars, based on 1 article reviews
Price from $9.99 to $1999.99
set a9 - by Bioz Stars, 2024-10
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Becton Dickinson set a9
Set A9, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/set a9/product/Becton Dickinson
Average 86 stars, based on 1 article reviews
Price from $9.99 to $1999.99
set a9 - by Bioz Stars, 2024-10
86/100 stars
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Becton Dickinson hu il 8 cba flex set a9 100tst
Active IL-16 promotes the production of IL-1β, IL-6, <t>IL-8,</t> and TNF (A) Correlation analysis between IL-16 and IL-6 using the Spearman correlation method. (B) Correlation analysis between IL-16 and IL-1β using the Spearman correlation method. (C) Representative analysis of IL-6 expression by CD45 + CD56 − CD3 + CD4 + T cells isolated from the RNE and EE. (D) Statistical analysis of the percentages of IL-6-producing T cells among the CD4 + T cell population isolated from the RNE (n = 9) and EE (n = 10), unpaired t test. Data represent a pool from multiple independent experiments. (E, G, and I) PBMCs from a healthy donor were cultured with or without active IL-16 (10 or 100 ng/mL). For the detection of TNF, each group of cells was treated with phorbol myristate acetate (50 ng/mL), ionomycin (1 μg/mL), and monensin (10 μg/mL). After 4 h, the expression of IL-6, TNF, and TGF-β1 was determined by intracellular staining. (F, H, and J) Statistical analysis of the percentages of IL-6 + , TNF + , and TGF-β1 + cells among the CD4 + T cell population, paired t test, IL-6 (n = 14), TNF (n = 9), and TGF-β1 (n = 9). Data in (E)–(J) represent a pool from multiple independent experiments. (K‒O) PBMCs from a healthy donor were stimulated for 12 h in the presence of PBS or different concentrations of active IL-16 (10 or 100 ng/mL), after which the production of IL-6, IL-1β, TNF, CXCL8, and TGF-β in cell supernatants was analyzed using a CBA assay, paired t test, n = 21. (P) PBMCs from a healthy donor were stimulated for 12 h in the presence of PBS or different concentrations of IL-6 (10 or 100 ng/mL), after which the production of IL-16 in cell supernatants was analyzed using ELISA, paired t test, n = 10. Data in (K)–(P) represent a pool from multiple independent experiments.
Hu Il 8 Cba Flex Set A9 100tst, supplied by Becton Dickinson, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/hu il 8 cba flex set a9 100tst/product/Becton Dickinson
Average 86 stars, based on 1 article reviews
Price from $9.99 to $1999.99
hu il 8 cba flex set a9 100tst - by Bioz Stars, 2024-10
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Thermo Fisher pcdna3 his set a9
Active IL-16 promotes the production of IL-1β, IL-6, <t>IL-8,</t> and TNF (A) Correlation analysis between IL-16 and IL-6 using the Spearman correlation method. (B) Correlation analysis between IL-16 and IL-1β using the Spearman correlation method. (C) Representative analysis of IL-6 expression by CD45 + CD56 − CD3 + CD4 + T cells isolated from the RNE and EE. (D) Statistical analysis of the percentages of IL-6-producing T cells among the CD4 + T cell population isolated from the RNE (n = 9) and EE (n = 10), unpaired t test. Data represent a pool from multiple independent experiments. (E, G, and I) PBMCs from a healthy donor were cultured with or without active IL-16 (10 or 100 ng/mL). For the detection of TNF, each group of cells was treated with phorbol myristate acetate (50 ng/mL), ionomycin (1 μg/mL), and monensin (10 μg/mL). After 4 h, the expression of IL-6, TNF, and TGF-β1 was determined by intracellular staining. (F, H, and J) Statistical analysis of the percentages of IL-6 + , TNF + , and TGF-β1 + cells among the CD4 + T cell population, paired t test, IL-6 (n = 14), TNF (n = 9), and TGF-β1 (n = 9). Data in (E)–(J) represent a pool from multiple independent experiments. (K‒O) PBMCs from a healthy donor were stimulated for 12 h in the presence of PBS or different concentrations of active IL-16 (10 or 100 ng/mL), after which the production of IL-6, IL-1β, TNF, CXCL8, and TGF-β in cell supernatants was analyzed using a CBA assay, paired t test, n = 21. (P) PBMCs from a healthy donor were stimulated for 12 h in the presence of PBS or different concentrations of IL-6 (10 or 100 ng/mL), after which the production of IL-16 in cell supernatants was analyzed using ELISA, paired t test, n = 10. Data in (K)–(P) represent a pool from multiple independent experiments.
Pcdna3 His Set A9, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/pcdna3 his set a9/product/Thermo Fisher
Average 86 stars, based on 1 article reviews
Price from $9.99 to $1999.99
pcdna3 his set a9 - by Bioz Stars, 2024-10
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Active IL-16 promotes the production of IL-1β, IL-6, IL-8, and TNF (A) Correlation analysis between IL-16 and IL-6 using the Spearman correlation method. (B) Correlation analysis between IL-16 and IL-1β using the Spearman correlation method. (C) Representative analysis of IL-6 expression by CD45 + CD56 − CD3 + CD4 + T cells isolated from the RNE and EE. (D) Statistical analysis of the percentages of IL-6-producing T cells among the CD4 + T cell population isolated from the RNE (n = 9) and EE (n = 10), unpaired t test. Data represent a pool from multiple independent experiments. (E, G, and I) PBMCs from a healthy donor were cultured with or without active IL-16 (10 or 100 ng/mL). For the detection of TNF, each group of cells was treated with phorbol myristate acetate (50 ng/mL), ionomycin (1 μg/mL), and monensin (10 μg/mL). After 4 h, the expression of IL-6, TNF, and TGF-β1 was determined by intracellular staining. (F, H, and J) Statistical analysis of the percentages of IL-6 + , TNF + , and TGF-β1 + cells among the CD4 + T cell population, paired t test, IL-6 (n = 14), TNF (n = 9), and TGF-β1 (n = 9). Data in (E)–(J) represent a pool from multiple independent experiments. (K‒O) PBMCs from a healthy donor were stimulated for 12 h in the presence of PBS or different concentrations of active IL-16 (10 or 100 ng/mL), after which the production of IL-6, IL-1β, TNF, CXCL8, and TGF-β in cell supernatants was analyzed using a CBA assay, paired t test, n = 21. (P) PBMCs from a healthy donor were stimulated for 12 h in the presence of PBS or different concentrations of IL-6 (10 or 100 ng/mL), after which the production of IL-16 in cell supernatants was analyzed using ELISA, paired t test, n = 10. Data in (K)–(P) represent a pool from multiple independent experiments.

Journal: Cell Reports Medicine

Article Title: Pyroptotic T cell-derived active IL-16 has a driving function in ovarian endometriosis development

doi: 10.1016/j.xcrm.2024.101476

Figure Lengend Snippet: Active IL-16 promotes the production of IL-1β, IL-6, IL-8, and TNF (A) Correlation analysis between IL-16 and IL-6 using the Spearman correlation method. (B) Correlation analysis between IL-16 and IL-1β using the Spearman correlation method. (C) Representative analysis of IL-6 expression by CD45 + CD56 − CD3 + CD4 + T cells isolated from the RNE and EE. (D) Statistical analysis of the percentages of IL-6-producing T cells among the CD4 + T cell population isolated from the RNE (n = 9) and EE (n = 10), unpaired t test. Data represent a pool from multiple independent experiments. (E, G, and I) PBMCs from a healthy donor were cultured with or without active IL-16 (10 or 100 ng/mL). For the detection of TNF, each group of cells was treated with phorbol myristate acetate (50 ng/mL), ionomycin (1 μg/mL), and monensin (10 μg/mL). After 4 h, the expression of IL-6, TNF, and TGF-β1 was determined by intracellular staining. (F, H, and J) Statistical analysis of the percentages of IL-6 + , TNF + , and TGF-β1 + cells among the CD4 + T cell population, paired t test, IL-6 (n = 14), TNF (n = 9), and TGF-β1 (n = 9). Data in (E)–(J) represent a pool from multiple independent experiments. (K‒O) PBMCs from a healthy donor were stimulated for 12 h in the presence of PBS or different concentrations of active IL-16 (10 or 100 ng/mL), after which the production of IL-6, IL-1β, TNF, CXCL8, and TGF-β in cell supernatants was analyzed using a CBA assay, paired t test, n = 21. (P) PBMCs from a healthy donor were stimulated for 12 h in the presence of PBS or different concentrations of IL-6 (10 or 100 ng/mL), after which the production of IL-16 in cell supernatants was analyzed using ELISA, paired t test, n = 10. Data in (K)–(P) represent a pool from multiple independent experiments.

Article Snippet: Hu IL-8 CBA Flex Set A9 100Tst , BD , 558277.

Techniques: Expressing, Isolation, Cell Culture, Staining, Enzyme-linked Immunosorbent Assay

Journal: Cell Reports Medicine

Article Title: Pyroptotic T cell-derived active IL-16 has a driving function in ovarian endometriosis development

doi: 10.1016/j.xcrm.2024.101476

Figure Lengend Snippet:

Article Snippet: Hu IL-8 CBA Flex Set A9 100Tst , BD , 558277.

Techniques: Recombinant, Protein Extraction, SYBR Green Assay, Bicinchoninic Acid Protein Assay, Multiple Displacement Amplification, Staining, Enzyme-linked Immunosorbent Assay, Sequencing, Software