Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2019 Aug 27;9:12421. doi: 10.1038/s41598-019-48741-w

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

PMC Copyright notice

LPM in SerpinB2^−/− and SerpinB2^+/+ mice. (a) Peritoneal lavage cells from SerpinB2^−/− and SerpinB2^+/+ mice were stained with CD11b and F4/80 and analyzed by FACS. Numbers (±SD) show the percentage of SPM and LPM (gates indicated) as a proportion of all peritoneal lavage cells (n = 3 mice per group). The F4/80^hi lines indicate the cut-off used to FACS sort LPM. (b) Immunofluorescent antibody staining of FACS-sorted LPM using anti-murine SerpinB2 antibody and FITC-phalloidin (F-actin) imaged using confocal microscopy. All three images for SerpinB2^+/+ LPM and SerpinB2^−/− LPM are of the same field. (c) Immunoblotting of LPM from SerpinB2^+/+ and SerpinB2^−/− mice using anti-murine SerpinB2 and anti-GAPDH antibodies. Full length gels are shown in Fig. S15.