The pre-university stream was divided into two onee course prepared students for the Sijil Tinggi Persekolahan Malaysia (STPM) standardised examination, lasting two years, while the other comprised various matriculation courses graded by individual lecturers, typically lasting a year.
On day 0, samples were prepared, divided into aliquots, and stored at 4°C, −20°C, or −80°C until analysis.
OMCS were prepared and divided into three groups according to storage period of cryopreservation (fresh (no cryopreservation), 4 week and 12 week cryopreservation groups).
A 1-mL volume of each diluted serum was prepared and divided into two aliquots of equal volume.
Forty-eight dentin slices were prepared and divided into 3 groups (n = 16) and filled with Angelus WMTA, Nano-WMTA, or Bioaggregate.
Bovine muscle tissues (n = 154) with standard sizes and weights were prepared and divided into two temperature groups: room temperature and 45 °C.
To evaluate the applicability of Q-PCR and the standard curve method to small tissue samples, RA synovial tissue lysates were prepared and divided into five aliquots for further processing.
Briefly, D2O solution of PEP (5 mM) in phosphate buffer (25 mM) was prepared and divided into 25 mL fractions, which were adjusted to seven pH values: 3.9, 5.95, 7.14, 8.07, 9.93, 11.12, and 12.11.
The stock aqueous solution of Thy (1 mg/ml) was first prepared and then divided into two aliquots.
Each fecal sample (1 g) was divided into 2 tubes that contained freshly prepared thioglycollate (40 mL) (Oxoid, Basingstoke, UK).
