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Monomer and oligomer desorption was minimized by imaging directly after adsorption; a loss of small aggregates species would likely be an issue for samples stored under a buffer at RT for a significant period of time.
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On their first visit to Syria in August, she said, team members came under sniper fire in a buffer zone between government- and opposition-held areas in the Damascus suburbs.
The lysate was loaded onto a Ni-NTA column (Qiagen) and the bound protein was eluted under denaturing conditions in a buffer containing 0.05 M Tris (pH 8.0), 0.3 M NaCl, 0.3 M imidazole and 8 M Urea.
Neocortices were harvested under sterile conditions in a buffer solution containing 137 mM NaCl, 5 mM KCl, 170 μM Na2HPO4, 205 μM KH2PO4, 5 mM glucose, 59 mM sucrose, 100 U/ml penicillin and 0.1 mg/ml streptomycin, pH 7.4.
Total protein extracts were prepared by glass-glass homogenization of mesenteric veins, pulverized under liquid nitrogen, with a buffer composed of (mM): 10 Tris-HCl (pH 7.4), 5 EDTA, 5 EGTA, 10 sodium pyrophosphate, 10 NaF, 1 sodium orthovanadate, 0.1 AEBSF and 0.001 leupeptin.
Preparative chromatography of IgG from human serum under a standardised buffer regime eluted IgG of ∼65% purity, compared to ∼62% with Protein G.
These reagents could react with the imino unit of thymine or guanine base on DNA or of uracil base on RNA under a basic buffer condition to yield a labeled product quantitatively in a short period of time.
Optimal focusing and resolution of all test steroids under a single buffer condition was realized by a dynamic pH junction-sweeping format using borate, pH 11.0 and bile acid surfactant with γ-CD in the BGE, whereas the sample is devoid of surfactant at pH 8.0.
Analytical column Dionex IonPac CS5A RFIC 4*250 mm was found to retain and separate species of interest the most effectively under the isocratic elution with a buffer, containing 50 mM ammonium citrate, 7.0 mM pyridine-2,6-dicarboxylic acid at pH = 4.2 and flow rate of 0.8 L min−1.
An assurance recorded was that apart that from creating a buffer zone under the declared heritage site, the steam trains would be retained within the site.
Individual mouse liver samples were ground into powder under liquid nitrogen, dissolved in a buffer containing 5 M urea, 2 M thiourea, 2% (w/v) CHAPS, 2% (w/v) Zwittergent 3-10 detergent (Calbiochem, Merck Biosciences, Darmstadt, Germany) 50 mM DTT (Sigma Aldrich, Milano, Italy) and protease inhibitor cocktail set III (Calbiochem).
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