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The beads were capped with a mixture of 10 mL 0.2 M phenoxyacetic anhydride in dry THF and 10 mL of 0.2 M 1-methyl imidazole and 0.2 M 2,4,6-trimethylpyridine in dry THF for 10 min at room temperature.
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Its teeth were capped with magnetite.
Sample vials were capped with Teflon-lined caps.
During amplification wells were capped with PCR cap strips.
Bottles were capped with ambient air headspaces.
They are capped with gold.
All pre-mRNAs are capped and associated with cap binding proteins (CBPs) to form the cap binding complex (CBC).
The electrostatic potential is capped from below to prevent singularities as beads exit the channel and interact with charges on the open LG.
The beads were washed twice with 400 µl of cap wash buffer (cap lysis buffer with 0,5% NP-40 instead of 1%) and twice with 500 µl of ice-cold PBS.
The beads were washed with crosslinking buffer.
The beads were washed with RIPA buffer.
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