Afterwards, microarrays were washed using Agilent Gene Expression Wash Buffer Kit and scanned with the Agilent DNA microarray scanner G2505B.
GeneChips were washed using the Gene Expression Wash Buffers Pack and scanned using an Agilent DNA Microarray Scanner (G2565CA).
Cells were washed using ice-cold PBSA buffer (1× PBS pH 7.4 supplemented with 0.1% w/v bovine SA fraction V).
Slides were washed using Agilent wash buffers.
Next, cells were washed using sterile phosphate buffered saline (PBS) (pH 7.4), 2-3 times.
After fixation, the samples were washed using PBS buffer solution containing (0.05% Tween-20).
Before incubation with secondary antibodies, the sections were washed using PBS (5-10 min) for three times.
These samples were washed using 60 μm nylon mesh and dry-sieved using 124 μm nylon mesh.
The following day, the slides were washed using PBS with 0.05% Tween (PBS-T, Sigma-Aldrich) for 5 min.
The unbound dNTPs were washed using wash buffer and anti-DIG-POD was added to the MTP.
Plant samples were washed using tap water and then rinsed with distilled water to remove the adhering soil.
