Mouse CXCL15/Lungkine DuoSet ELISA

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Ancillary Products Available
Mouse CXCL15 / Lungkine ELISA Standard Curve
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Product Details
Citations (8)
Supplemental Products

Mouse CXCL15/Lungkine DuoSet ELISA Summary

Assay Type
Solid Phase Sandwich ELISA
96-well strip plate
Assay Length
4 hours 40 minutes (after plate preparation)
Sample Volume Required
100 µL
Assay Range
125.0 - 8,000 pg/mL
Sufficient Materials
For fifteen 96-well plates*
Please see the product datasheet

* Provided that the recommended microplates, buffers, diluents, substrates and solutions are used, and the assay is run as summarized in the Assay Procedure provided.

This DuoSet ELISA Development kit contains the basic components required for the development of sandwich ELISAs to measure natural and recombinant mouse CXCL15/Lungkine. The suggested diluent is suitable for the analysis of most cell culture supernate samples. Diluents for complex matrices, such as serum and plasma, should be evaluated prior to use in this DuoSet.

Product Features

  • Optimized capture and detection antibody pairings with recommended concentrations save lengthy development time
  • Development protocols are provided to guide further assay optimization
  • Assay can be customized to your specific needs
  • Economical alternative to complete kits

Kit Content

  • Capture Antibody
  • Detection Antibody
  • Recombinant Standard
  • Streptavidin conjugated to horseradish-peroxidase (Streptavidin-HRP)

Other Reagents Required

DuoSet Ancillary Reagent Kit 2 (5 plates): (Catalog # DY008) containing 96 well microplates, plate sealers, substrate solution, stop solution, plate coating buffer (PBS), wash buffer, and Reagent Diluent Concentrate 2.

Normal Goat Serum: (Catalog # DY005)


The components listed above may be purchased separately:

PBS: (Catalog # DY006), or 137 mM NaCl, 2.7 mM KCl, 8.1 mM Na2HPO4, 1.5 mM KH2PO4, pH 7.2 - 7.4, 0.2 µm filtered

Wash Buffer: (Catalog # WA126), or 0.05% Tween® 20 in PBS, pH 7.2-7.4

Reagent Diluent: (Catalog # DY995), or 1% BSA in PBS, pH 7.2-7.4, 0.2 µm filtered

Substrate Solution: 1:1 mixture of Color Reagent A (H2O2) and Color Reagent B (Tetramethylbenzidine) (Catalog # DY999)

Stop Solution: 2 N H2SO4 (Catalog # DY994)

Microplates: R&D Systems (Catalog # DY990)

Plate Sealers: ELISA Plate Sealers (Catalog # DY992)

Normal Goat Serum: (Catalog # DY005)


Scientific Data

Mouse CXCL15 / Lungkine ELISA Standard Curve

Product Datasheets

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Preparation and Storage

The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
Stability & Storage
Store the unopened product at 2 - 8 °C. Do not use past expiration date.

Background: CXCL15/Lungkine

CXCL15/Lungkine, also named WECHE, is a member of the ELR motif-containing CXC chemokines.

Entrez Gene IDs:
20309 (Mouse)
Alternate Names:
CXCL15; Il8; IL-8; Lungkine; Scyb15; Weche

Assay Procedure


Plate Preparation

  1. Dilute the Capture Antibody to the working concentration in PBS without carrier protein. Immediately coat a 96-well microplate with 100 μL per well of the diluted Capture Antibody. Seal the plate and incubate overnight at room temperature.
  2. Aspirate each well and wash with Wash Buffer, repeating the process two times for a total of three washes. Wash by filling each well with Wash Buffer (400 μL) using a squirt bottle, manifold dispenser, or autowasher. Complete removal of liquid at each step is essential for good performance. After the last wash, remove any remaining Wash Buffer by aspirating or by inverting the plate and blotting it against clean paper towels.
  3. Block plates by adding 300 μL Reagent Diluent to each well. Incubate at room temperature for a minimum of 1 hour.
  4. Repeat the aspiration/wash as in step 2. The plates are now ready for sample addition.

Assay Procedure

  1. Add 100 μL of sample or standards in Reagent Diluent, or an appropriate diluent, per well. Cover with an adhesive strip and incubate 2 hours at room temperature.
  2. Repeat the aspiration/wash as in step 2 of Plate Preparation.
  3. Add 100 μL of the Detection Antibody, diluted in Reagent Diluent with NGS, to each well. Cover with a new adhesive strip and incubate 2 hours at room temperature.
  4. Repeat the aspiration/wash as in step 2 of Plate Preparation.
  5. Add 100 μL of the working dilution of Streptavidin-HRP to each well. Cover the plate and incubate for 20 minutes at room temperature. Avoid placing the plate in direct light.
  6. Repeat the aspiration/wash as in step 2.
  7. Add 100 μL of Substrate Solution to each well. Incubate for 20 minutes at room temperature. Avoid placing the plate in direct light.
  8. Add 50 μL of Stop Solution to each well. Gently tap the plate to ensure thorough mixing.
  9. Determine the optical density of each well immediately, using a microplate reader set to 450 nm. If wavelength correction is available, set to 540 nm or 570 nm. If wavelength correction is not available, subtract readings at 540 nm or 570 nm from the readings at 450 nm. This subtraction will correct for optical imperfections in the plate. Readings made directly at 450 nm without correction may be higher and less accurate.

Citations for Mouse CXCL15/Lungkine DuoSet ELISA

R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.

8 Citations: Showing 1 - 8
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  1. Galectin-3 inhibitor GB0139 protects against acute lung injury by inhibiting neutrophil recruitment and activation
    Authors: DC Humphries, R Mills, C Boz, BJ McHugh, N Hirani, AG Rossi, A Pedersen, HT Schambye, RJ Slack, H Leffler, UJ Nilsson, W Wang, T Sethi, AC Mackinnon
    Frontiers in Pharmacology, 2022;13(0):949264.
    Species: Mouse
    Sample Types: BALF
  2. Effects of G-Rh2 on mast cell-mediated anaphylaxis via AKT-Nrf2/NF-kappaB and MAPK-Nrf2/NF-kappaB pathways
    Authors: C Xu, L Li, C Wang, J Jiang, L Li, L Zhu, S Jin, Z Jin, JJ Lee, G Li, G Yan
    Journal of Ginseng Research, 2022;46(4):550-560.
    Species: Mouse
    Sample Types: BALF
  3. Indole-3-lactic acid associated with Bifidobacterium-dominated microbiota significantly decreases inflammation in intestinal epithelial cells
    Authors: AM Ehrlich, AR Pacheco, BM Henrick, D Taft, G Xu, MN Huda, D Mishchuk, ML Goodson, C Slupsky, D Barile, CB Lebrilla, CB Stephensen, DA Mills, HE Raybould
    BMC Microbiol, 2020;20(1):357.
    Species: Mouse
    Sample Types: Cell Culture Supernates
  4. Role of biomarkers and effect of FIP-fve in acute and chronic animal asthma models
    Authors: CT Wu, YT Lee, MS Ku, KH Lue
    J Microbiol Immunol Infect, 2020;0(0):.
    Species: Mouse
    Sample Types: BALF
  5. Artesunate exerts protective effects against ulcerative colitis via suppressing Toll?like receptor 4 and its downstream nuclear factor?kappaB signaling pathways
    Authors: YX Chen, XQ Zhang, CG Yu, SL Huang, Y Xie, XT Dou, WJ Liu, XP Zou
    Mol Med Rep, 2019;20(2):1321-1332.
    Species: Rat
    Sample Types: Cell Culture Supernates
  6. Inhalation of hydrogen gas attenuates airway inflammation and oxidative stress in allergic asthmatic mice
    Authors: N Zhang, C Deng, X Zhang, J Zhang, C Bai
    Asthma Res Pract, 2018;4(0):3.
    Species: Mouse
    Sample Types: BALF
  7. Lack of SOCS3 increases LPS-induced murine acute lung injury through modulation of Ly6C(+) macrophages
    Authors: Z Jiang, Z Chen, L Li, W Zhou, L Zhu
    Respir. Res., 2017;18(1):217.
    Species: Mouse
    Sample Types: BALF
  8. Anti-inflammatory effects of Perilla frutescens leaf extract on lipopolysaccharide-stimulated RAW264.7 cells.
    Authors: Huang B, Lin C, Chen Y, Kao S
    Mol Med Rep, 2014;10(2):1077-83.
    Species: Mouse
    Sample Types: Cell Culture Supernates


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