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The mix was boiled for 5 minutes then diluted with water to reach spectrophotometer linear range.
Then, the mix was boiled for 8 min at 100°C and vortexed again.
The reaction mix was boiled for 5 min and color development was monitored at 625 nm [ 29].
The mix was boiled for 10 min, to denature secondary structures, and slowly cooled to room temperature to allow primers to anneal.
The reaction mix was boiled for 5 min and the supernatant was collected and loaded on a precast 4-20% SDS-PAGE.
The reaction mix was boiled for 5 minutes prior to cooling on ice and the addition of 2.5 μl of Spectral labeling buffer (Spectral Genomics, Houston, U.S.A), 1.5 μl of either Cy3-dCTP (1mM, Applied Biosystems, Foster City, U.S.A) or Cy5-dCTP (1 mM, Applied Biosystems) and 1 μl of Klenow Fragment (BioPrime labeling kit, Invitrogen).
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After the mix is boiled, it is poured through an oxtail filter and served in small porcelain cups with sugar cubes.
After mixing, the mixture was boiled for 5 min, cooled and filtrated.
Lysates or protein mixes were boiled at 95°C with 1× SDS Laemmli sample buffer, for 5 min before being subject to SDS PAGE (8 or 10% Tris glycine gel, or 4 10% gradient gels (Life Technologies) or self-prepared 16% bis-acrylamide).
The kettle was boiling.
My blood was boiling.
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