The largest database of trusted experimental protocols

Msd mouse proinflammatory panel 1 5 plex kit

Manufactured by Mesoscale
Sourced in United States

The MSD Mouse Proinflammatory panel 1 V-Plex kit is a multiplex assay designed to measure the levels of specific inflammatory biomarkers in mouse samples. The kit utilizes Mesoscale's proprietary electrochemiluminescence technology to quantify the concentrations of these analytes in a single sample.

Automatically generated - may contain errors

4 protocols using msd mouse proinflammatory panel 1 5 plex kit

1

Multiplex Serum Cytokine Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Serum samples were analyzed in duplicates according to the manufacturers’ instructions using a MSD Mouse Proinflammatory panel 1 V-Plex kit (MULTI-ARRAY®, Meso Scale Discovery, Gaithersburg, MD) and a Bio-Plex Pro Mouse Diabetic Assay (MAGPIX, Bio-Rad, Copenhagen, Denmark). Serum cytokines, chemokines and hormones analyzed were IFN-γ, IL-1β, IL-2, IL-4, IL-5, IL-6, IL-10, IL-12p70, KC/GRO, and TNF-α using MSD and glucagon, insulin, leptin, monocyte chemotactic protein-1 (MCP-1), and regulated upon activation, normal T cell expressed and secreted (RANTES) using Bio-Plex (Bio-Rad).
+ Open protocol
+ Expand
2

Comprehensive Metabolic and Inflammatory Profiling

Check if the same lab product or an alternative is used in the 5 most similar protocols
Serum cholesterol, low-density lipoprotein cholesterol and very low-density lipoprotein (LDL/VLDL), glucose, triacylglycerol (TAG), total protein concentrations, uric acid, non-esterified fatty acids (NEFA; D07940, Dialab, Austria) and total antioxidant status (TAS; NX2332 Randox Total Antioxidant Status, Randox Laboratories Ltd., UK) were analysed using conventional enzymatic kits and a MaxMat PLII bioanalyser (MaxMat PL, Montpellier, France). Unless otherwise stated all kits were from MaxMat PL (Montpellier, France). Serum oxidized LDL (Ox-LDL) was quantified in duplicates according to the manufacturers’ instruction with a murine ELISA-kit (E90527Mu, USCN Life Science Inc., Texas, US). Serum samples were analysed in duplicates for the following cytokines: interferon gamma (IFNγ), interleukin 10 (IL-10), interleukin 1 beta (IL-1β), interleukin 2 (IL-2), interleukin 5 (IL-5), interleukin 6 (IL-6), keratinocyte chemoattractant growth-regulated oncogene (KC-GRO), and tumour necrosis factor alpha (TNF-α). These analyses were performed according to the manufacturers’ instructions using a MSD Mouse Proinflammatory panel 1 V-Plex kit (MULTI-ARRAY®, Meso Scale Discovery, Gaithersburg, MD).
+ Open protocol
+ Expand
3

Profiling Peripheral Inflammation in Mice

Check if the same lab product or an alternative is used in the 5 most similar protocols
Plasma samples collected from three time points: 1) two hours after the first chronic injection (acute), 2) two hours after the final chronic injection (chronic), and 3) from trunk blood at the time of tissue collection (terminal; seven to eight days after a trigger LPS injection used for cognitive testing) to assess markers of peripheral inflammation. Circulating concentrations of IFN-γ, IL-1ß, IL-2, IL-4, IL-5, IL-6, IL-10, IL-12p70, KC/GRO, and TNF-α were assessed using the MSD V-Plex Proinflammatory Panel 1 Mouse Kit (Meso Scale Diagnostics, Rockville, MD, USA; Cat. #: K15048D-2) and read using the MESO QuickPlex SQ 120 (Meso Scale Diagnostics). A standard curve was completed to determine the required dilutions for analysis. Based on results from the standard curve, samples from saline treated mice were diluted 1:8 for both the acute and chronic time points. Samples from LPS treated mice were diluted 1:20 and 1:30 for acute and chronic time-points respectively. All terminal time points regardless of treatment history were diluted 1:2. MSD workflow was completed according to manufacturer instructions.
+ Open protocol
+ Expand
4

Peripheral Inflammation Biomarkers Profiling

Check if the same lab product or an alternative is used in the 5 most similar protocols
Plasma samples collected from three time points: 1) two hours after the first chronic injection (acute), 2) two hours after the final chronic injection (chronic), and 3) from trunk blood at the time of tissue collection (terminal; seven to eight days after a trigger LPS injection used for cognitive testing) to assess markers of peripheral inflammation. Circulating concentrations of IFN-γ, IL-1ß, IL-2, IL-4, IL-5, IL-6, IL-10, IL-12p70, KC/GRO, and TNF-α were assessed using the MSD V-Plex Proinflammatory Panel 1 Mouse Kit (Meso Scale Diagnostics, Rockville, MD, USA; Cat. #: K15048D-2) and read using the MESO QuickPlex SQ 120 (Meso Scale Diagnostics). A standard curve was completed to determine the required dilutions for analysis.
Based on results from the standard curve, samples from saline treated mice were diluted 1:8 for both the acute and chronic time points. Samples from LPS treated mice were diluted 1:20 and 1:30 for acute and chronic time-points respectively. All terminal time points regardless of treatment history were diluted 1:2. MSD workflow was completed according to manufacturer instructions.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!