The largest database of trusted experimental protocols

10 protocols using mouse mpo elisa kit

1

Ischemic Brain Biomarker Quantification

Check if the same lab product or an alternative is used in the 5 most similar protocols
Hemoglobin (Hb), myeloperoxidase (MPO), and interleukin (IL-6) content was measured by ELISA (Mouse Hemoglobin ELISA Kit, ab157715—Mouse MPO ELISA kit, ab155458; Abcam, Paris, France—Mouse IL-6 ELISA Kit, 88-7064-88, eBioscience, Santa Clara, USA) using brain homogenates prepared from TTC sections. Hb, MPO, and IL-6 concentration values were reported on total protein content from the ischemic hemisphere.
+ Open protocol
+ Expand
2

Quantitative ELISA Analyses of Inflammatory Markers

Check if the same lab product or an alternative is used in the 5 most similar protocols
The mouse MPO ELISA kit was purchased from Abcam (Cat. No. ab275109), PYY ELISA kit from Aviva Systems Biology (Cat. No. OKCD05062, USA), mouse TNF-α and IL-6 ELISA kits from Biolegend (Cat. No. 431,301 and 430,901, USA). The protocols were performed as the manufacturers described. In brief, 96-well plates were coated with the corresponding capture antibody. After incubation with blocking buffer (PBS + 1% bovine serum albumin), a 100-µl aliquot of either standards, serum, or colonic protein extracts (5 mg tissue per mL PBS supplemented with protease inhibitors) was added into each well individually and the plates were incubated for 2 h at room temperature. The detector antibody was added to the wells, the plate was incubated, and unbound detector antibody was removed by washing. The avidin-peroxidase conjugate was added, the plate was incubated, and unbound conjugate was removed by washing. The enzymatic reaction catalyzed by horseradish peroxidase (HRP) was initiated by adding the substrate, 3,3’,5,5’ tetramethylbenzidine dihydrochloride (TMB). The absorbance was measured by using a microplate reader at a wavelength 450 nm after the reaction was stopped with 2 M H2SO4.
+ Open protocol
+ Expand
3

Metabolic Biomarkers in Diabetic Mice

Check if the same lab product or an alternative is used in the 5 most similar protocols
The concentrations of AMP, GMP, ADSS, and IMPDH2 in BM fluid of db/db mice were measured using an ELISA. The enzymatic activity of ADSS and IMPDH2 in lineage−/low cells were also determined by ELISA, in accordance with the manufacturer’s instructions (MLBio, Shanghai, China). Plasma lipase and amylase activities were measured using commercial kits and quantified by a Tecan Safire microplate reader as previously described12 (link). Plasma levels of myeloperoxidase (MPO) were determined using a Mouse MPO ELISA Kit (Abcam, Shanghai, China).
+ Open protocol
+ Expand
4

Cytokine and MPO Quantification

Check if the same lab product or an alternative is used in the 5 most similar protocols
The levels of IL-6, and IL-1β in lung homogenates were measured by ELISA (R&D Systems). The lung myeloperoxidase (MPO) levels were determined using lung tissue homogenates using a mouse MPO ELISA kit (Catalog #ab155458; Abcam), according to manufacturer’s instructions.
+ Open protocol
+ Expand
5

Cytokine and MPO Profiling in Colitis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Cytokine levels such as interleukin (IL)-6, tumor-necrosis factor (TNF)-α, and monocyte chemoattractant protein (MCP)-1 in the serum and colon were determined using a ProcartaPlex Mouse Cytokine panel (Thermo Fisher Scientific, Waltham, MA, USA) according to the manufacturer’s instructions and detected using a Luminex MAGPIX System (Luminex, Austin, TX, USA). The colonic MPO activity was assessed using the Mouse MPO Elisa Kit (Abcam, Cambridge, MA, USA) according to the manufacturer’s instructions.
+ Open protocol
+ Expand
6

NET-associated MPO and Cytokine Quantification

Check if the same lab product or an alternative is used in the 5 most similar protocols
Blood was collected into EDTAK2 anticoagulant (10% v/v). After centrifugation of whole blood at 1000 G for 5 min at 4 °C, plasma was collected, and the cell pellet was removed. NETs-associated MPO was captured on coated 96-well plates from the mouse MPO ELISA kit (Abcam, Cambridge, UK, Roche, Basel, Switzerland). After washes, the incubation buffer containing a peroxidase-labeled antieDNA monoclonal antibody (dilution 1:10) were added to each well. Then, the peroxidase substrate (ABTS) was added after several washes. Last, absorbance at a wavelength of 405 nm was measured. Cytokines: Interleukin (IL)-6, IL-10, interferon-γ (IFN-γ), tumor necrosis factor-alpha (TNF-α), macrophage inflammatory protein 2 (MIP-2), and monocyte chemoattractant protein-1(MCP-1) were measured using Luminex® xMAP according to the manufacturer’s instructions. A standard curve was used to calculate the concentrations of cytokines.
+ Open protocol
+ Expand
7

Quantification of Plasma Cytokines and Cholesterol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Plasma levels of IL-10 and IL-6 were assessed via ELISA by use of a commercially available kit (SA Biosciences, Germany). Measurements were performed in accordance with the manufacturer’s instructions. First, the samples were transferred into antibody-coated wells. After 120 min of incubation at room temperature, unbound sample was washed away and the detection antibodies were added, followed by 60 min of incubation at 37°C. Subsequently, the samples were incubated with Avidin-HRP and the development reagent for 30 min in the dark. Absorbance was measured using a photometer (Tecan Austria, Austria). MPO plasma levels were measured by use of a Mouse MPO ELISA Kit (Abcam, U.K.). The measurements were performed in duplicate, exactly as advised by the manufacturer, by using 75 μL of EDTA Plasma. Blood cholesterol levels were assessed by use of gas chromatography–flame ionization detection.
+ Open protocol
+ Expand
8

Assessing Inflammation Markers in Colon Tissue

Check if the same lab product or an alternative is used in the 5 most similar protocols
The NF-κB activity was measured using the Phospo-NF-κB p65 ELISA kit (RayBiotech, Inc., Norcross, GA, USA) following extraction of the nuclear protein from colon tissue using a Nuclear Extraction Kit (Abcam, Cambridge, UK). Myeloperoxidase (MPO) levels were determined in the colon tissue homogenates using a Mouse MPO ELISA kit (Abcam, Cambridge, UK). PGE2 concentration was determined using the Prostaglandin E2 (PG-E2) ELISA kit (Cusabio, Wuhan, China) according to the manufacturer’s protocol. Absorbance was determined using a microplate reader (Varioskan Flash, Thermo Fisher Scientific, Waltham, MA, USA). Results were normalized to total protein concentration, determined by the bicinchoninic acid (BCA) assay (BCA Protein Assay Kit, Thermo Fisher Scientific, Pittsburgh, PA, USA).
+ Open protocol
+ Expand
9

Quantifying Vitiligo Biomarkers and Oxidative Stress

Check if the same lab product or an alternative is used in the 5 most similar protocols
The diagnostic markers of vitiligo [tyrosinase (TYR), macrophage migration inhibitory factor (MIF) and monoamine oxidase (MAO)] were quantified using Mouse Tyrosinase ELISA kit (cat. no. MBS763418; MyBioSource, Inc.), Mouse MIF ELISA kit (cat. no. ab209885; Abcam) and Mouse monoamine oxidase ELISA kit (cat. no. MBS731375; MyBioSource, Inc.) respectively according to manufacturer's instructions. Additionally, Cu/Zn superoxide dismutase ELISA kit (cat. no. QIA97; Merck Millipore), MDA Assay Kit (cat. no. ab238537; Abcam). and Mouse MPO ELISA kit (cat. no. ab155458; Abcam) were correspondingly used to measure superoxide dismutase (SOD), malondialdehyde (MDA) and myeloperoxidase (MPO) in serum based on competitive binding between antibodies.
+ Open protocol
+ Expand
10

Quantification of NET-associated MPO and cytokines

Check if the same lab product or an alternative is used in the 5 most similar protocols
Blood was collected into EDTAK2 anticoagulant (10% v/v). After centrifugation of whole blood at 1000G for 5 minutes at 4, plasma was collected, and the cell pellet was removed. NET-associated MPO was captured on coated 96-well plates from the mouse MPO ELISA kit (Abcam, Cambridge, UK, Roche, Basel, Switzerland). Cytokines: Interleukin (IL)-6, IL-10, Interferon-γ (IFN-γ), Tumor Necrosis Factor-alpha (TNF-α), Macrophage Inflammatory Protein 2 (MIP-2) and Monocyte Chemoattractant Protein-1(MCP-1) were measured using Luminex ® xMAP according to the manufacturer's instructions. A standard curve was used to calculate the concentrations of MPO-DNA and cytokines.
+ 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!