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3 protocols using nucblue fixed cell readyprobes dapi

1

Senescence Cells Histochemical Staining

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Senescence staining was performed according to the manufacturer’s instructions using a Senescence Cells Histochemical Staining Kit (Sigma Aldrich, Cat. No: CS0030) and we reported previously [25 (link)]. Briefly, cells were fixed and stained with an X-gal staining mixture for 37°C for 3 h. Frozen tissue samples were prepared as described above. About 10 µm thick sections of mouse tissues were air-dried on the slide glasses (Matsunami Glass, Osaka, Japan) for 40 min, surrounded with a pap-pen, fixed with a fixation solution (Sigma Aldrich, Cat. No: CS0030) for 20 min, washed with 1×P BS for 10 min at RT. Tissues were then incubated with an X-gal staining mixture (Sigma Aldrich, Cat. No: CS0030) for 37°C for 24 h. Then tissues were washed with PBS for 10 min, stained with NucBlue™ Fixed Cell ReadyProbes™ (DAPI, Invitrogen, Cat. No: R37606, Lot No: 2216969) for 5 min, and washed three times with 1× PBS for 10 min each. Samples were imaged using a Keyence microscope (Keyence corp.) via bright field imaging.
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2

Immunohistochemical Analysis of Tissue Sections

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After treatments, the tissues were transferred to Tissue-Tek optimal cutting temperature (O.C.T, Sakura Finetek, Tokyo, Japan) compound to snap freeze for immunohistology. IHC was done as previously described [32 (link),34 (link)]. Briefly, 10 µm tissue sections were air-dried on the slide glasses (Matsunami Glass, Osaka, Japan) for 40 min at RT, then washed with tris-buffered saline with 0.1% Tween20 (1× TBST) for 10 min. Tissues were blocked with 3% bovine serum albumin (BSA Gemini, Bio-Products, West Sacramento, CA, U.S.A.)/1× TBST for 1 h followed by overnight incubation with vimentin diluted at 1:300 (Abcam, Cat. No.: ab92547, Lot No.: GR3186827-13) and cytokeratin-18 diluted at 1:800 (Abcam, Cat. No: ab668, Lot No: GR3196069-6) in 3% BSA/1× TBST at 4°C. The next day, tissues were washed 3 times with 1× TBST for 10 min each, then treated with secondary antibodies diluted at 1:1000 (Alexa Fluor® 488, Abcam, Cat. No.: ab150073, Lot: GR269274-4 and Alexa Fluor™ 594, Invitrogen, Cat. No.: A11005, Lot: 2179228, respectively) in 3% BSA/1× TBST for 3 h at RT. Then, tissues were stained with NucBlue™ Fixed Cell ReadyProbes™ (DAPI, Invitrogen, Cat. No: R37606, Lot No: 2216969) for 5 min, and washed 3 times with 1× TBST for 10 min each. The images were taken with a Keyence microscope (Keyence Corp., Osaka, Japan).
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3

Molecular Mechanisms of LMP1 Signaling Pathway

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P19C and P19 were synthesized in GL Biochem (Shanghai) Ltd.
The LMP1
antibody was purchased from Abcam. The antibodies including anti-LMP1
were purchased from kerafast, while anti-NF-κB p65, anti-NF-κB
p105/50, antihistone H3, and anti-GAPDH were purchased from Cell Signaling
Technology. Antirabbit IgG HRP-linked, antimouse IgG HRP-linked, and
protease/phosphatase inhibitor cocktail were purchased from Cell Signaling
Technology. Alexa Fluor 488-conjugated goat antimouse IgG, NucBlue
fixed cell ready probes (DAPI), and ProLong gold antifade mountant
with DAPI were purchased from Invitrogen. The transcriptional response
element (TRE)-fluorescent protein reporter, pTRE-EGFP plasmid, was
constructed as previously reported.44 (link)
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