Sentence examples for serum samples were mixed from inspiring English sources

The diluted serum samples were mixed with 50 PFU of MHV-68 and incubated on ice for 1 h.

The diluted serum samples were mixed with an equal volume of media containing homotypic influenza virus at a concentration of 1050%% tissue culture infectious dose/well.

Serially diluted serum samples were mixed with equal volumes of CHIKV suspensions at a multiplicity of infection of 10 and inoculated into baby hamster kidney cells.

The serial dilutions of serum samples were mixed with equal volume of PRRSV strains: VR-2332, KS-06, or NVSL97-7895 containing 200 TCID50 of the virus.

Serial 2-fold dilutions of serum samples were mixed in equal volume with 100-fold the median tissue culture infective dose (TCID50) of H1N1 (X-181) virus, in 96-well tissue culture plates, and incubated 1 h at 37 °C.

In a 96-well plate, 5 μL serum samples were mixed with 0.5 mM Gly-Pro-4-Me-β-NA in 50 mM Tris buffer (pH 8.3) in a final volume of 110 μL.

An aliquot of 400 µl of each serum sample was mixed with 500 µl lysis buffer (RLT, Qiagen, Valencia, CA) and 800 µl acid phenol: Chloroform (Ambion, Foster City, CA), vortexed for 30 seconds and centrifuged at 16000 rcf for 10 min at 25°C.

Protein concentrations were determined by Bradford assay (Bio-Rad Laboratories, HerCAles, CA) with bovine serum albumin (BSA) as standard, and samples were mixed with equal volume of 2 x SDS sample buffer (125 mM Tris-HCl, pH 6.8, 4 % SDS, 20%% glycerol, 0.1 % mercaptoethanol).

For APTT assay, 25 μL of tested samples were mixed with 50 μL of citrated normal rabbit serum, and then APTT assay reagent was added.

Samples were mixed every 5 min.

The samples were mixed by gentle tapping.