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The murine lung sections were initially evaluated after being stained with hematoxylin and eosin.
The murine lung sections incubated with buffer without primary antibody were maintained as negative controls and consistently stained negative for red precipitates (not shown).
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Sections of murine lung tissue served as positive controls for specific staining of integrin β6.
Immunohistochemical analysis of tissue sections of murine lung adenomas as well as human lung adenocarcinomas, squamous cell carcinomas and non-small cell lung carcinomas showed consistently higher expression of GPER in the tumor relative to the surrounding non-tumor tissue.
Chromatin was extracted from murine lung tumors (FFPE slides) starting from the equivalent of 4×, 2×, 1×, 0.5×, and 0.25× FFPE lung sections.
Necropsies were performed, and trachea and lung sections were stained with hematoxylin and eosin and by an immunocytochemistry technique that involved a murine monoclonal antibody specific to EIV hemagglutinin.
(E ) Lung sections were stained with a human-specific anti-vimentin antibody to detect human tumor cells in the murine lung.
Expression of the integrin subunit alpha8 in murine lung development.
Gibbings, S. L. et al. Three unique interstitial macrophages in the murine lung at steady state.
Mujahid S, Logvinenko T, Volpe MV, Nielsen HC. miRNA regulated pathways in late stage murine lung development.
Knockdown of ACTN4 expression in murine lung fibroblasts significantly impaired cell migration, spreading, adhesion, and proliferation.
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