The largest database of trusted experimental protocols

Mouse cxcl1 kc duoset elisa kit

Manufactured by R&D Systems
Sourced in Germany

The Mouse CXCL1/KC DuoSet ELISA kit is a quantitative sandwich enzyme-linked immunosorbent assay (ELISA) designed to measure mouse CXCL1/KC in cell culture supernates, serum, and plasma.

Automatically generated - may contain errors

7 protocols using mouse cxcl1 kc duoset elisa kit

1

CXCL1 Measurement in Tissue Homogenates

Check if the same lab product or an alternative is used in the 5 most similar protocols
Liver and lung tissue were homogenized in protein lysis buffer at 4 °C, followed by centrifugation for 30 min at 4 °C at 20,000×g. Supernatants were stored at − 80 °C for later analyses of protein concentration of CXCL1 using a Mouse CXCL1/KC DuoSet ELISA kit of R&D Systems according to manufacturer’s instructions (Wiesbaden-Nordenstadt, Germany). ELISA was performed using the Infinite M200 microplate reader (Tecan, Männedorf, Switzerland).
+ Open protocol
+ Expand
2

IL-8 Secretion in Fn-infected EDMs

Check if the same lab product or an alternative is used in the 5 most similar protocols
Supernatants were collected from WT, NEIL2 KO EDMs, and APCMin/+ polyp either uninfected or infected with Fn. IL-8 (KC) was measured using the mouse CXCL1/KC DuoSet ELISA kit (R & D Systems) according to the manufacturer’s instructions. The level of IL-8 was compared between Fn-infected EDMs vs. the uninfected EDMs from WT, Neil2 KO mice, and APCMin/+ polyp.
+ Open protocol
+ Expand
3

Quantifying Protein Levels in HBEC and BAL Fluid

Check if the same lab product or an alternative is used in the 5 most similar protocols
Protein levels in the supernatants of HBECs or BAL fluid were analyzed by ELISA. For HBEC samples, human IL‐8 ELISA MAX Deluxe Set (BioLegend, 431504), human CXCL1/GRO alpha DuoSet ELISA (R&D Systems, DY275‐05), and human IL‐29/IL‐28B (IFN‐lambda 1/3) DuoSet ELISA kit (R&D Systems, DY1598B‐05) were used according to the manufacturers’ instructions. For BAL fluids, a mouse CXCL1/KC DuoSet ELISA kit (R&D Systems, DY453‐05) was used as instructed by the manufacturer. The data were acquired with a Ledetect 96 Microplate reader (Labexim Products, Lengau, Austria). Online analysis software Myassays.com and a four‐parameter logistic regression model were used to calculate the concentrations of the proteins.
+ Open protocol
+ Expand
4

Quantifying Plasma Biomarkers in Murine Injury Models

Check if the same lab product or an alternative is used in the 5 most similar protocols
To assess plasma concentrations of cTnI, keratinocyte chemoattractant (KC) and monocyte chemotactic protein-1 (MCP-1), sandwich-enzyme-linked immunosorbent assay (ELISA) based kits were used adhering to manufacturers’ instructions: mouse CXCL1/KC DuoSet ELISA Kit (R&D Systems, Germany), Ultra-Sensitive Mouse Cardiac Troponine-I ELISA (Life Diagnostics, USA), Mouse MCP-1 ELISA Kit (BD Biosciences, USA). For determining plasma C3a levels, a monoclonal rat anti-mouse anti-C3a antibody (BD Biosciences, USA) was used for antigen detection according to standard ELISA protocol. Recombinant mouse complement component C3a (R&D Systems, Germany) served for calculation of a standard curve.
To rule out dilution effects due to resuscitation procedure, all results were normalized to the respective amount of total plasma protein. Total amount of protein in plasma was evaluated, using a Pierce Bicinchoninic Acid (BCA) Assay (Thermo Fisher Scientific, USA).
Blood hemoglobin was evaluated by standard blood gas analysis (ABL 700 blood gas analysis device; Radiometer, Denmark).
+ Open protocol
+ Expand
5

Cytokine Profiling of Lung Cancer Secretome

Check if the same lab product or an alternative is used in the 5 most similar protocols
Conditioned media from lung adenocarcinoma cells was collected as described above for C2C12 studies. Cytokine arrays were performed using Proteome Profiler Mouse XL Cytokine Arrays (R&D Systems) and visualized/quantified using a LI-COR Odyssey FC system. Ectopic cytokine studies were performed using C2C12 cells plated at a density of 100–500K/well of a 6-well tissue culture dish and differentiated as noted above for conditioned media experiments. All cytokines were purchased from Peprotech and used as noted in the text based on published IC50 ranges defined in other cell types/experimental contexts: IGFBP3 (cat#: 100-008), IGFBP6 (cat#: 350-07B), CXCL1 (cat#: 250-11), LIX/CXCL6 (cat#: 250-17), CCL2 (cat#: 250-10), CCL17 (cat#: 300-30), CCL20 (cat#: 250-27), and endostatin (cat#: 150-01). We noted substantial lot-to-lot variability with the CXCL1 preparations, so we advise recalibrating phenotypes if using different cytokine lots. CXCL1 ELISAs were performed using a Mouse CXCL1/KC DuoSet ELISA kit (R&D Systems) and serum or liquid nitrogen prepared whole muscle lysates from terminal tumor-bearing (531LN2) mice.
+ Open protocol
+ Expand
6

Quantifying CXCL1 in EAE Mice

Check if the same lab product or an alternative is used in the 5 most similar protocols
Blood was collected via submandibular bleeding from control mice and EAE-induced diseased mice at 9, 21, and 40 dpi. These time points were selected to represent disease onset, disease peak time, and disease late phase, respectively. Serum was isolated and stored at − 80 °C until CXCL1 measurement with a mouse CXCL1/KC Duo set ELISA kit (#DY453, R&D Systems).
+ Open protocol
+ Expand
7

Measuring IL-8 in Fn-infected EDMs

Check if the same lab product or an alternative is used in the 5 most similar protocols
Supernatants were collected from WT., NEIL2 KO EDMs and APC Min polyp either uninfected or infected with Fn. IL-8 (K.C.) was measured using the mouse CXCL1/KC DuoSet ELISA kit (R&D Systems) according to the manufacturer's instructions. The level of IL-8 was compared between Fn infected EDMs versus the uninfected EDMs from WT., NEIL2 KO mice and APC Min/+ polyp.
+ 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!