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Blocks were kept in 30% sucrose solution overnight.
The bone blocks were kept in 10% buffered formalin solution for 24 hours, washed in running water for 24 hours, and gradually dehydrated in a series of alcohol solutions ranging from 70 to 100% ethanol.
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One task consisted of 6 blocks, presented in random order while stimuli in each block were kept in the same sequence.
Each block was kept in different sealed envelopes.
Data are fetched in blocks of 8 Kb, and each block is kept in a cache.
A possibility of ciliary block glaucoma owing to prolonged unrelieved angle closure was kept in mind [ 6, 7].
For histochemical analyses, paraffin blocks were kept at −20°C.
Computer generated multi-block 1 1 randomizations were kept in sealed opaque envelopes.
In West 2006, participants were randomly assigned to one of three intervention arms using a computer-generated sequence with a variable block size, and assignments were kept in opaque containers until needed, leading to a low risk of bias.
After the washing steps (3 × 5 min) with PBS, cells were kept in blocking buffer 3% BSA for 1 h.
Slides were kept in blocking buffer with 10% normal goat serum and 0.3% Triton solution for 1 h at room temperature and washed with PBS three times.
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