Sentence examples for buffer sections were processed from inspiring English sources

After thorough rinsing in buffer, sections were processed with the avidin biotin technique, using a commercial kit.

As negative controls, sections were processed without terminal deoxynucleotidyltransferase (TdT) buffer.

Then, the sections were processed in 10 mmol/L citrate buffer (pH = 6.0) and heated to 121°C in an autoclave for 20 min to retrieve the antigen.

Tissue areas of ∼0.25 cm from three 10- μm-thick sections were processed in 100  μl of extraction buffer.

For the immunohistochemistry study, paraffin sections were processed for antigen retrieval with 10 mM citrate buffer (pH 6.0), and then processed in the same manner as the frozen sections.

For negative controls, serial sections were processed with the primary antibody replaced by the dilution buffer alone.

Sections were processed for immunohistofluorescence; blocking solution was PBS (phosphate buffered saline)/0.25%gelatin/5%% normal donkey serum/0.3% Triton.

The FFPE sections were processed with the Dako EnVision™ FLEX antigen retrieval EDTA buffer (pH 9) for 20 minutes at 97°C using DAKO PT Link module (PT Link, Dakocytomation, Denmark) according to the manufacturer's instructions.

The sections were processed to unmask the antigens by conventional microwave oven heating in 10 m M citric acid buffer (pH 6.0) for 12 min.

De-waxed and hydrated sections were processed in a microwave oven for 3 cycles, 5 min each, at 450 W in citrate buffer, pH 6.0.

Sections were processed as previously described [23].