Chromatin Immunoprecipitation: Difference between revisions

Iharvey (talk | contribs)
Iharvey (talk | contribs)
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# Add 200 μl PBS/BSA (for each sample you plan to use this antibody with) to beads.
# Add 200 μl PBS/BSA (for each sample you plan to use this antibody with) to beads.
# Add 1 μg primary antibody. Mix gently by tapping--Do not vortex beads after adding the antibody.
# Add 1 μg primary antibody. Mix gently by tapping--Do not vortex beads after adding the antibody.
# Gently mix on a rotator platform for at least 2 hours at 4°C.
# Gently mix on a rotator platform for at least '''2 hours''' at 4°C.
# Wash beads 3 times (steps b-c), resuspending the beads by inverting the tubes during each wash.
# Wash beads 3 times (steps b-c), resuspending the beads by inverting the tubes during each wash.
# Resuspend in 100 μl  PBS/BSA (for each sample you plan to use this antibody with), and proceed to Step 2.
# Resuspend in 100 μl  PBS/BSA (for each sample you plan to use this antibody with), and proceed to Step 2.