In this video, we describe the immunofluorescence method to visualize the localization of the DNA repair proteins γH2AX and 53BP1 at the sites of double-strand DNA breaks in irradiated cell nuclei.
Protocol
1. Nuclear extraction and cell fixation Prepare stock solutions: 0.2 M PIPES (pH 6.8), 5 M NaCl, 2 M sucrose, 1 M MgCl2, 0.1 M EGTA (pH 8.0). Prepare nuclear extraction buffer (NEB): dissolve 10 mM PIPES (pH 6.8), 100 mM NaCl, 300 mM sucrose, 3 mM MgCl2, 1 mM EGTA (pH 8.0) and 0.5% (v/v) Triton X-100 in ddH2O. Mix until dissolved completely. Prepare 4% (v/v) paraformaldehyde (PFA): dissolve 10 mL of 16% PFA aqueous solution in 30 mL PBS. Mi…
Representative Results
Figure 1. Nuclear extraction. Representative images of cells prior to (left) and post (right) nuclear extraction. Cytoplasm should be digested but the nuclear structure should remain intact post-extraction (right). (A) 20x magnification; scale bar = 20 μm and (B) 40x magnification; scale bar = 10 μm.
Açıklamalar
The authors have nothing to disclose.
Materials
Coverglass #1, 18 mm round (coverslips)
Neuvitro
NC0308920
Coverslips need to be cleaned and sterilized prior using, with HCl or ethanol.
DPBS, no calcium, no magnesium
Gibco
14190144
PBS for tissue culture
SlowFade Diamond Antifade Mountant with DAPI
Invitrogen
S36973
300 nM DAPI with VECTASHIELD Antifade Mounting Medium can be used instead.
Bovine serum albumin (BSA)
Sigma-Aldrich
A3059
Heat-shock fraction is recommended, to avoid precipitation/background.