Feb 26, 2024

Public workspaceSOP for LBP ELISA after DSS-induced injury

  • 1College of Medicine |University of Florida
Open access
Protocol CitationMalu G Tansey 2024. SOP for LBP ELISA after DSS-induced injury. protocols.io https://dx.doi.org/10.17504/protocols.io.q26g7pk73gwz/v1
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License,  which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: January 29, 2024
Last Modified: May 31, 2024
Protocol Integer ID: 94307
Keywords: ASAPCRN
Funders Acknowledgement:
Aligning Science Across Parkinson’s (ASAP)
Grant ID: ASAP-020527
Abstract
SOP for LBP ELISA after DSS-induced injury
Protocol
Protocol
Concentrations of plasma LPS-binding protein (LBP) were examined via Mouse LBP SimpleStep ELISA according to the manufacturer’s protocol (Abcam, #ab269542).
Plasma samples were prepared at a 1:16,000 dilution.
Standards, antibody cocktail containing detector and capture antibodies, and 1x wash buffer were prepared according to the manufacturer’s protocol.
In the plate, 50µL of standard or sample was added to appropriate wells in duplicate.
50µL of antibody cocktail was added to all wells.
The plate was then incubated at RT for 1 hour on a plate shaker at 400 rpm.
Wells were decanted and washed three times with 150µL 1x wash buffer.
100µL of TMB Development Solution was added to each well and allowed to incubate in the dark for 12 minutes with shaking at 400rpm
100µL of Stop Solution was added to each well and placed on the shaker for 1 minute at 400 rpm to mix.
Absorbance of 450nm light was recorded with a FLUOstar Omega microplate reader (BMG Labtech).
The standard curve was created by plotting the blank-subtracted average LBP standard absorbance against the standard LBP concentrations.
Sample LBP concentrations were calculated by interpolating the blank-subtracted average absorbance values against the standard curve, multiplied by the dilution factor.