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Immunofluorescence images underlying figure 9 and figure 10 from paper Role of Aggregative Adherence Fimbriae

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posted on 2024-05-15, 18:00 authored by Angela Melton-CelsaAngela Melton-Celsa, Viktoria Van NederveenViktoria Van Nederveen, Ennzo Ortega, Anthony Soc, Mark A. Smith

Images of mouse cecum and colon staining for EAEC bacteria by immunofluorescence

Methods: On day 4 for D5613, and day 5 post-infection for K411, mice were humanely euthanized as dictated by the approved protocol. Mouse ceca and colons were collected, fixed in formalin, embedded in paraffin, then further processed onto glass slides. For immunofluorescent detection of EAEC, unstained tissue sections on slides were deparaffinized with Histo-Clear (National Diagnostics), then treated with Antigen Unmasking Solution (Vector Laboratories) as per manufacturers’ protocols. Tissue sections were then incubated with 1:100 of anti-O154 (D5613) or anti-O128abc (K411) antibody from SSI diagnostica (Hillerød, Denmark) then with 1:200 goat anti-rabbit Alexa 488 (RRID: AB_2576217). As a counterstain for cell nuclei, SlowFade Diamond Antifade Mountant with DAPI (4’,6-diamidino-2-phenylindole) (Invitrogen) was used to mount coverslips.

Disclaimer: The opinions and assertions expressed herein are those of the authors and do not reflect the official policy or position of the Uniformed Services University of the Health Sciences or the Department of Defense. References to non-Federal entities or products do not constitute or imply a Department of Defense or Uniformed Services University of the Health Sciences endorsement. The opinions and assertions expressed herein are those of the authors and do not reflect the official policy or position of the Henry M. Jackson Foundation for the Advancement of Military Medicine, Inc. Neither the authors nor any family members have a financial interest in any commercial product, service, or organization providing financial support for this research.


Funding

MIC-73-12977

MIC-73-3373

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