Serum LPS was measured as described previously (de La Serre et al. 2015). LPS was quantified using a Pyrochrome Lysate Mix, a quantitative chromogenic reagent, (Associate of Cape Cod, MA) diluted in Glucashield buffer which inhibits cross-reactivity with (1→3)-β-D-Glucans. Briefly, serum samples were diluted 1:10 in Pyrogen free water (Lonza, Switzerland) and heated for 10 min at 70°C. Samples and reactive solution were incubated at 37°C for 30 min and absorbance was read at 405 nm.
Do you have any questions about this protocol?
Post your question to gather feedback from the community. We will also invite the authors of this article to respond.
 Tips for asking effective questions
+ Description
Write a detailed description. Include all information that will help others answer your question including experimental processes, conditions, and relevant images.