Sentence examples for an equal solution of from inspiring English sources

The protein content was determined using a BCA protein assay kit [ 35– 37] and a standard curve of known concentrations of bovine serum albumin (BSA) (25 2000 μg/ml) in an equal solution of 0.1 M NaOH containing 5%% SDS (sodium dodecyl sulfate) and 0.1 M HCl.

The blank gel formulation was prepared with the same described procedure, but replacing the protein solution with an equal volume of physiological solution (NaCl 0.9%).

Optimal crystals were formed by mixing 1.8 μl of protein solution with an equal volume of reservoir solution containing 0.1 M Tris/HCl (pH 7.0), 0.05 M CdSO4 and 0.3 M sodium acetate and growing for 3 days at 277 K.

A 30-μl aliquot of bacterial suspension was mixed with saline solution or an equal volume of TBO solution at the various concentrations (100, 500, and 1000 μg/ml) in the wells of a sterile 96-well flat bottom plate (Falcon®; Becton Dickinson Co., NJ).

The leukocytes were labeled by mixing whole blood with an equal volume of solution containing LDS-751 (Molecular Probes).

About 400 μg desalted peptide mixture was mixed with an equal volume of solution A and loaded onto the HAMMOC tips (100 μg mixed peptides per tip).

In detail, the rEhMCF protein suspension (see the section above) was mixed with an equal volume of solution containing liposomes into which one of the countersubstrates examined was preloaded.

After 30 min, the protoplasts were centrifuged at 15000 g for 4 min and resuspended in an equal volume of solution (0.4 M mannitol, 15 mM MgCl2, and 4 mM MES, pH 5.7) to allow the protoplasts to swell.

0.5 µl of sample was mixed with an equal volume of matrix solution (saturated solution of cyano-4-hydroxycinnamic acid (HCCA) in 65% water/35% acetonitrile/0.1% trifluor acetic acid (TFA)) and applied onto a MALDI target by the dried-droplet method.

Briefly, crystals of 2-ME-SOD1 were produced from a mixture of 100 mg/ml protein solution and an equal amount of a reservoir solution containing 15% (w/v) PEG3350/300 mM (NH4 2SO4 at pH 6.0 after being equilibrated against the reservoir solution by hanging drop vapour diffusion at a temperature of 16°C.

Crystals of diffraction quality were grown at 18°C using the sitting drop method for FXR1 and hanging drop method for FXR2 by mixing an equal volume of protein solution with reservoir solution.