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Cba mouse cytokine assay kits

Manufactured by BD
Sourced in United States

The BD CBA Mouse Cytokine assay kits are laboratory equipment designed to quantify multiple mouse cytokines simultaneously in a single sample. The kits use flow cytometry to measure the concentration of various cytokines in biological samples.

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5 protocols using cba mouse cytokine assay kits

1

Cytokine Detection in Leishmania Infection

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For CBA multiplex cytokine detection, cells were plated, primed as described above and incubated with LPGs, GIPLs, LPS and live stationary promastigotes (MOI 10:1) for 48 h. Leishmania braziliensis LPG (10 μg/mL) was added as a positive control [21 (link)]. For negative controls fresh medium was added. Supernatants were collected and IL1-β, IL-6, IL-10, IL-12p40 and TNF-α were determined using the BD CBA Mouse Cytokine assay kits according to the manufacturer’s specifications (BD Biosciences, CA, USA). Flow cytometry measurements were performed on a FACS Calibur flow cytometer (Becton Dickinson, Mountain View, CA). Cell-Quest™ software package provided by the manufacturer was used for data acquisition and the FlowJo software 7.6.4 (Tree Star Inc., Ashland, OR, USA) was used for data analysis. A total of 2,400 events were acquired for each preparation. Results are representative of two experiments in duplicate. Nitrite concentrations were determined by Griess reaction [21 (link)].
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2

Multiplex Cytokine Detection in Supernatants

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For CBA multiplex cytokine detection, supernatants were collected and cytokines were determined using the BD CBA Mouse Cytokine assay kits according to the manufacturer's specifications (BD Biosciences). IL-1β, IL-2, IL-3, IL-4, IL-5, IL-6, IL-10, IL-12/IL-23p40, IL-17, IFN-γ and TNF-α were measured. Flow cytometry measurements were performed on a FACSCalibur flow cytometer (BD Biosciences). Cell-Quest™ software package provided by the manufacturer was used for data acquisition, and the FlowJO software 7.6.4 (Tree Star, Inc., Ashland, OR) was used for data analysis. A total of 2,400 events were acquired for each preparation. Nitrite concentrations were determined by Griess reaction (Griess Reagent System, 2009).
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3

Cytokine and Nitrite Quantification

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The cytokines TNF-α, IL-6, and IL-10 were determined using BD CBA Mouse Cytokine Assay kits according to the manufacturer's specification (BD Biosciences, CA, USA). Flow cytometry measurements were performed on a FACSCalibur flow cytometry (BD Bioscience, CA, USA) collected using the Cell-QuestTM software package provide by the manufacturer (1200 events). FlowJO software 7.6.4 (Tree Star, Inc, Ashland, OR) was used for data analysis. Results are representative of two experiments in triplicate. Nitrite concentration (NO) was determinate by Griess Reaction as described (Nogueira et al., 2015 (link)).
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4

Assay of Macrophage Responses to LPGs

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Thioglycollate-elicited peritoneal macrophages were extracted from C57BL/6 and C57BL/6 (TLR2 and TLR4 knockouts) as previously reported (Ibraim et al., 2013 (link); Nogueira et al., 2016 (link)). Briefly, recovered cells (3 × 105 cells/well) were washed with fresh RPMI and cultured in the same medium supplemented with 2 mM glutamine, 50 U/ml of penicillin and 50 μg/mL streptomycin, 10% Fetal Bovine Serum in 96-well culture plates (37°C, 5% CO2). Cells were primed with gamma interferon (IFN-γ) (3 IU/mL) for 18 h prior to incubation with LPGs (10 μg/mL) from all strains and controls for 48 h. Those included LPS (100 ng/mL, positive) and medium (negative). The nitrite concentration was measured by Griess reaction. For cytokine detection, supernatants were collected and IL-1β, IL-6, IL-12, and TNF-α were determined using BD CBA Mouse Cytokine assay kits according to the manufacturer's specifications (BD Biosciences, CA, USA). Flow cytometry measurements were performed on a FACS Calibur flow cytometry (BD Bioscience, Mountain View, CA, USA). Cell-Quest TM software package provided by the manufacturer was used for data acquisition and the FlowJo software 7.6.4 (Tree Star Inc., Ashland, OR, USA) was used for data analysis (Nogueira et al., 2016 (link)).
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5

Cytokine Profiling in Leishmaniasis

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For CBA multiplex cytokine detection, cells were plated, primed as describe above and incubated with LPGs and live stationary promastigotes (MOI 10:1) for 48 h. LPS was added as a positive control and medium as negative control. Supernatants were collected and IL-1β, IL-6, IL-10, IL-12p40 and TNF-α were determined using BD CBA Mouse Cytokine assay kits according to the manufacturer’s specifications (BD Biosciences, CA, USA). Flow cytometry measurements were performed on a FACSCalibur flow cytometry (BD Bioscience, Mountain View, CA, USA). Cell-QuestTM software package provided by the manufacturer was used for data acquisition and the FlowJo software 7.6.4 (Tree Star Inc., Ashland, OR, USA) was used for data analysis. A total 1,500 events were acquired for each preparation. Results are representative of six experiments in duplicate. Nitrite concentrations were determinate by Griess reaction (Griess Reagent System, 2009).
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