Nghĩa của từ buffer solution bằng Tiếng Việt

Dung dịch đệm

Đặt câu có từ "buffer solution"

1. Moreover, the alkalinity measurement is difficult in the presence of a buffer solution

2. To our Buffer solution, we're gonna add some strong acids so a source of …

3. Mix 825 ml of acetate buffer solution (3.9) with 175 ml of acetonitrile (3.2).

4. A Buffer solution needs to have substantial amounts of both present and that's what I'm trying to represent over here

5. How Buffers Work In order to understand how a buffer works, consider the example of a buffer solution made by dissolving sodium acetate into acetic acid

6. A Buffer solution is one in which the pH of the solution is "resistant" to small additions of either a strong acid or strong base

7. Check for amylolytic activity : mix 100 ml starch solution (3.18), 5 ml buffer solution (3.4), 0 75 ml sodium chloride solution (3.5) and 62 75 mg pancreatin.

8. C) Acetified with acetic acid The only kidney biopsy tissue available has been fixed in phosphate buffered glutaraldehyde for 2 hours and then placed in phosphate buffer solution

9. This buffer solution can be kept for at least four weeks at # °C.#.NADP (nicotinamide adenine dinucleotide phosphate, disodium salt) solution: Dissolve # mg of NADP in # ml of water

10. Introduction to Buffers (Opens a modal) Buffers, the acid rain slayer (Opens a modal) Common ion effect and Buffers (Opens a modal) Buffers and Henderson-Hasselbalch (Opens a modal) Buffer solution pH calculations

11. Electron microscopy: Samples of the leaf, Auricles, ligule and inflorescences were fixed in a 2.5% glutaraldehyde and 2% parafonnaldehyde solution in a 0.1 M sodium phosphate buffer, pH 7.4 (Karnovsky 1965) and were rinsed with the buffer solution.

12. A Buffer solution (more precisely, pH Buffer or hydrogen ion Buffer) is an aqueous solution consisting of a mixture of a weak acid and its conjugate base, or vice versa.Its pH changes very little when a small amount of strong acid or base is added to it

13. For refolding of the constructs, the purified protein was diluted to a concentration of 250 μg/ml with the denaturing buffer in a 50 ml dialysis bag and subjected to a stepwise urea-removal dialysis (protein solution/buffer solution 1:50, v/v) against borate buffers (0.9% Boracic acid/0.3% NaOH, pH 9.5) containing 4, 2, 1 or 0 M urea.

14. Lipid Aliquots were transferred to vials where the bulk of the chloroform was removed with a stream of argon.: We switched to individual Aliquots of buffer solution, prepared in single-use tubes.: The cooled, clear digest was diluted to 20 ml with distilled water, filtered, and Aliquots were taken for analyses.: Sample digestion for Hg analysis was conducted separately, using 5 g Aliquots of