Examples of 'mm sodium' in a sentence
Meaning of "mm sodium"
The phrase 'mm sodium' does not have a specific meaning in English. It appears to be a combination of two unrelated terms, 'mm' which can stand for millimeter, and 'sodium' which is a chemical element. Without further context, it is unclear how these two terms are being used together
How to use "mm sodium" in a sentence
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mm sodium
In a particular embodiment about 6 mM sodium butyrate is used.
For example, 10 mM sodium phosphate may be used for the mobile phase.
Diafiltration against at least five retentate volumes of 50 mM sodium chloride is generally suitable.
A buffering system of 10 mM sodium phosphate was evaluated during the LCS experiments.
In certain other embodiments, the aqueous ophthalmic solution comprises 3 mM sodium acetate.
The incubations were carried out with 10 mM sodium cholate as activating bile salt.
The appropriate fractions are pooled and diluted with an equal volume of 20 mM sodium acetate.
The solution is then pulled into a syringe . mM Sodium Glycocholate Preparation Method,.
The antibodies are concentrated by ultrafiltration and returned to a PBS buffer containing 1 mM sodium azide.
All samples were dialysed thoroughly against 50 mM sodium chloride to remove uncoupled dye.
A 10 mM sodium phosphate buffer pH 7.5 was also added up to the final working volume.
Quantitation was based on a standard curve generated with a 10 mM sodium monobasic phosphate standard.
Treatment of glycoproteins with 1 mM sodium periodate at 0°C oxidizes sialic acid groups to possess carbonyls.
After completion of the reaction, the reaction mixture was immersed in a 1 mM sodium acetate buffer.
The pepsin is reconstituted in 20 mM sodium acetate buffer adjusted to pH 4 with acetic acid.
See also
Of penicillin and streptomycin, and 1 mM sodium pyruvate.
Four-hundred milliliters of 400 mM sodium chloride was added to the precipitates obtained.
The solutions contain less than 75 mM sodium chloride.
For example, 10 mM sodium phosphate has been found to be suitable.
The product was eluted with 10 mM sodium acetate.
A 1.00 mM sodium phosphate solution is used to generate a standard curve for the assay.
The column is equilibrated with a 10 mM sodium phosphate buffer.
At least 50 mM sodium phosphate buffer is needed to dissolve up to 20 mM HQS.
The filter is postwashed with a 10 mM sodium chloride solution.
The eluent was 67 mM sodium phosphate buffer pH 7.4 with different amounts of BCD.
The elution buffer may comprise 50 mM sodium phosphate.
The mobile phase buffer was 10 mM sodium phosphate buffer supplemented with 20 % ethanol by volume.
The first three results are enhanced by 33 mM sodium pyruvate.
Mobile phase B contained 500 mM sodium chloride dissolved in mobile phase A.
The columns were equilibrated using buffer containing 10 mM sodium phosphate.
Regarding phosphate buffering, 25 mM sodium phosphate at pH 6.8 was determined to be optimal.
The vehicle used for drug administration was 50 mM sodium bicarbonate.
Approximately 24 hours later 2 mM sodium butyrate was added to each 10 cm plate.
The conjugate was eluted in the same buffer containing 20 mM sodium chloride.
The aqueous receptor solution was 15 mM sodium chloride buffered to pH 7 with 10 mM imidazole.
The buffering agent used in each aqueous composition was 10 mM sodium citrate.
The slide is then placed in 10 mM sodium citrate buffer pH 6.0 in a dish or jar.
The hydroxyapatite was washed with the equilibration buffer followed by 20 ml of 10 mM sodium phosphate.
Thereafter, the solvent was exchanged for 20 mM sodium chloride by using an ultrafilter.
Thereafter, the elution was carried out on a concentration gradient of from 50 to 650 mM sodium chloride.
In particular, in one experiment rituximab and 25 mM sodium citrate buffer were used as samples.
In one embodiment, the lyophilized pharmaceutical composition may comprise 10 to 100 mM sodium chloride.
Fractions eluted with about 55 mM to about 75 mM sodium chloride formed a peak of sugar content.
In one aspect, the sodium chloride solution that is added comprises about 40 mM sodium chloride.
PBS was used as the buffer and 10 mM sodium succinate as the chelator.
Further, the elution was sufficiently carried out in the same column with 650 mM sodium chloride.
Unadsorbed proteins were washed out with 50 mM sodium phosphate buffer containing 1 M NaCl.
The EG III cellulase component is eluted with an aqueous solution of 200 mM sodium chloride.
The bound protein was eluted with 20 mM sodium phosphate pH 7 at a flow rate of 2 ml / min.
The haemoglobin, concentrated on the filter was washed twice with 50 mM sodium phosphate buffer.
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