Übersetzung für "Millimolar" in Deutsch

The test compounds are employed as 50 millimolar (mM) solutions in dimethyl sulfoxide (DMSO).

The test compounds are employed as 50 millimolar (mM) solutions in dimethyl sulphoxide (DMSO).

The test compounds were employed as 50 millimolar (mM) solutions in dimethyl sulfoxide (DMSO).

In SDS concentrations above 0.1 millimolar, the unfolding of proteins begins, and above 1 mM, most proteins are denatured.

The detection of hydrogen peroxide with a chromogen as a coloring reagent, which is directly converted into a coloring substance because of the enzyme reaction, occurs by means of a solution which contains two international units of the enzyme horseradish peroxidase (POD) as well as a coloring reagent in the form of a millimolar 2.2' acino-bis-(3-ethylbenzthiazoline-6-sulphonic acid) in a 0.1 molar TRIS-HCl-buffer pH 8Ø

The precipitation of protein thus formed was centrifuged and the centrifuged mass dissolved in 20 ml KHPO4 /KH2 PO4 -buffer solution (50 millimolar, pH=7.4).

It is advantageous to use a completely different method, i.e. absorption on hydroxyapatite, before or after the rechromatography on ion exchangers, since this process is carried out with small losses and rapidly because the polypeptide according to the invention flows through the separating column unretarded in the conventionally used 10 millimolar phosphate buffer at pH 6.8, and only concomitant substances are bonded (cf. FIG. 3).

Buffer system: Borax/HCl buffer from Riedel-de Haen, pH 8.0, was mixed in the ratio 1:1 with a 10 millimolar solution of EDTA disodium salt in water and adjusted to pH 6.6 using HCl.

Buffer system: Borax/HCl buffer from Riedel-de Haën, pH 8.0, was mixed in the ratio 1:1 with a 10 millimolar solution of EDTA disodium salt and adjusted to pH 6.3 using HCl.

For this purpose the aqueous dispersion of solid particles is diluted with a pH-neutral 10 millimolar (mM) aqueous potassium chloride solution (standard potassium chloride solution) until the concentration of solid particles is from about 50 to 100 mg/l.

The amino acid glycine is used at a higher millimolar concentration, as glycine prevents the hypoxia-induced sodium influx by stabilizing the plasma membrane (prevention of a diffusion-oriented substance exchange) at these concentrations, and additionally inhibits the activation of macrophages.

For this purpose the aqueous dispersion of solid particles is diluted with a pH-neutral 10 millimolar (mM) potassium chloride solution (standard potassium chloride solution) until the concentration of solid particles is from about 50 to 100 mg/l.

The calculation of the enzyme activity takes place in that, as millimolar absorption coefficient for 2,6-dichlorophenol-indophenol at pH 7.5, there is assumed a value of 100.

The neutralized sample is mixed with 3 millimolar copper sulfate solution in a 1/9 ml/ml ratio and separated into components by HPLC on a stereospecific column, which are subsequently analyzed using a UV detector at a wavelength of 238 nm.

In order to make a preferential formulation of a drug for topical use, the method of choice is to dissolve the dichloric acids and/or the peroxochlorous acid or their derivatives, according to the invention, as salts in bidistilled water with concentrations in the lower millimolar or in the upper micromolar range—preferably in the concentration range of 0.5-5 mM with the pH equal to or >10, in particular 10 to 13, most preferably e.g. pH 11.5 and adjust the solution to isotonie with glycerine or common salt or another suitable well-tolerated, preferably physiological agent.

When all the bacteria under investigation have been applied to the test sites of the sample support, two microliters of a ten millimolar ammonium bicarbonate buffer (pH 8) is pipetted onto each one, whereby imipenem and bacteria mix with each other, and the bacterial cells are mostly not digested.