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Rabbit anti mouse desmin

Manufactured by Cell Signaling Technology
Sourced in United States

Rabbit anti-mouse desmin is a primary antibody that recognizes the intermediate filament protein desmin. Desmin is a structural protein found in skeletal, cardiac, and smooth muscle cells. This antibody can be used to detect and localize desmin in various cell and tissue samples.

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2 protocols using rabbit anti mouse desmin

1

Cryosectioning and Immunostaining of Murine Livers

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Livers were fixed in 4% PFA solution for 2 hours at room temperature and incubated in 30% sucrose solution for 24 hours. After fixation, livers were embedded in Tissue-Tek O.C.T. Compound (Sakura Finetek) on dry ice and cut into 10 μm sections using a cryostat (Leica). Liver sections were fixed using 4% PFA for 10 min and incubated in block solution (10% BSA in PBS) for 1 hour. Sections were permeabilized using 0.2% Triton-X 100 for 30 min and incubated in primary antibodies for 24 hours at 4 °C (Rat anti-mouse CD31 (Biolegend), rat anti-mouse CD68 (Biolegend), rabbit anti-mouse desmin (Cell Signaling)). After 24 hours, sections were washed (PBS containing 2% BSA) 3 times and incubated in secondary antibodies for 30 min (goat anti-rat secondary antibody, Alexa Fluor 488 conjugate (Thermo Fischer Scientific)). Coverslips were mounted using VECTASHIELD anti-fade mounting medium with DAPI (Vector Labs).
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2

Immunofluorescence Imaging of Liver Tissue

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NF-κB nuclear translocation and HBeAg cellular localization were detected with monoclonal antibody to P65, and GST tag. For NF-κB nuclear translocation, Alexa Fluor® 488 or 594-conjugated secondary antibodies (Abcam, Cambridge, UK) were incubated for 2 h. Nuclei were stained with 4′,6-diamidino-2-phenylindole (DAPI, Abcam, Cambridge, UK). Double immunofluorescence staining of α-SMA and F4/80 was conducted on liver cryosections and incubated overnight with primary rat anti-mouse F4/80 (Abcam, Cambridge, UK) and rabbit anti-mouse-α-SMA (Cell-Signaling Technology, Boston, USA) and then with secondary antibodies and DAPI. Immunolocalization of Desmin and ki67 was performed on liver cryosections and incubated with primary rat anti-mouse ki67 (Thermo Fisher Scientific, Waltham, MA) and rabbit anti-mouse-Desmin (Cell-Signaling Technology, Boston, USA). Images were captured using a fluorescence microscope (Olympus BX63, Tokyo, Japan) or confocal fluorescence microscopy (Leica TCS SP8).
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