Sentence examples for cold sodium from inspiring English sources

Ten mL of ice cold sodium hydroxide (0.5 M) were added to stop the reaction after 30 min incubation.

The study also revealed that the side pool of cold sodium plays a significant role in decay heat removal.

The resulting solution was poured into crushed ice and stirred well with a glass rod and cold sodium hydroxide solution (2 M) was added slowly with stirring until the pH was 8.

Tissue homogenate (50 μl) was added to 900 μl of cold sodium phosphate buffer (0.1 M containing 0.1% Triton X-100, pH 8.0) and 50 μl of 5,5-dithiobis (2-nitrobenzoic acid) (6 mM), then vortexed, and allowed to stand at room temperature for 10 min. Aliquots of 200 μl in triplicate were then placed into microtiter plate wells.

Frozen dorsolateral prostate and tumor samples were resuspended in cold sodium phosphate buffer (0.1M, pH 7.0) and lysed by sonication.

The regions were immediately homogenized with ice cold sodium dodecyl sulfate (SDS) sample buffer (20% glycerol, 10% β-mercaptoethanol and 20% SDS, 2.33 gr bromophenol blue in 62.5 mM Tris-HCl, pH 6.8) was added to each remaining lysate, thoroughly mixed and denatured 5 min at 95°C.

The cell pellet was resuspended in cold sodium-Tris-EDTA lysis buffer [10 mmol/L Tris (pH 8.0), 1 mmol/L EDTA, and 150 mmol/L NaCl] supplemented with lysozyme (1 mg/mL; Sigma) and incubated on ice for 15 minutes.

The material she used was a cloud of ultra-cold sodium atoms: scientifically fascinating, but of little practical use.

Cells were re-suspended in 250 μl of ice-cold sodium phosphate (100 mM, pH 6.5) and sonicated on ice.

Hemolymph phenoloxidase activity was estimated using 10 μl of hemolymph sample diluted in 1 ml of ice-cold sodium cacodylate buffer (0.01 M Na-cacodylate and 0.005 M CaCl2) and directly frozen in liquid N2.

These tissues were minced and separately homogenized (10% w/v) using a homogenizer (Potter-Elvehjem) in ice-cold sodium potassium phosphate buffer (0.01 M, pH 7.4) containing 1.15% of KCl.