Примери за използване на Final dilution на Английски и техните преводи на Български
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Medicine
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Colloquial
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Ecclesiastic
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Ecclesiastic
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Step 2: Second(final) dilution for infusion.
For a test sample of one gram multiply the volume of the final dilution(v4) by five.
After final dilution in the infusion bag/bottle.
V4= the aliquot volume in ml of the final dilution(to 100 millilitres).
For the final dilution add ten millilitres of the solution(4.5) to the 100 millilitre graduated flask.
This is equivalent to 1/4 final dilution of serum.
However, the final dilution volume may vary depending on the patient' s clinical status and physician discretion.
Solution for IV infusion after final dilution(see package leaflet).
If a solvent other than the mobile phase is used to dissolve the test and reference substances,the mobile phase should be used for the final dilution prior to injection.
Serum titres of less than 1/4(final dilution) are considered negative in these cases.
Copper solution(dilute): dilute 10 ml of stock solution(3.6) to 100 ml with water and then dilute 10 ml of the resulting solution, to 100 ml with water,1 ml of the final dilution contains 10 µg of copper(Cu).
PGR Mix Master allows the user to specify a product, final dilution volume(in gallons), and dilution concentration(PPM).
Antibody titres are expressed as the final dilution of tests serum giving 50% of the mean OD value recorded in the virus control wells where test serum is absent.
If possible, an assay is required if toxic components are present andif the quality cannot be controlled on final dilution to be incorporated because of the high dilution degree.
All of the materials used including raw materials and intermediates up to the final dilution to be incorporated into the finished homeopathic veterinary medicinal product, accompanying the application shall be supplemented by additional data on the homeopathic stock.
Every step of the manufacturing process from the starting materials up to the final dilution to be incorporated into the finished product must be fully described.
Every step of the manufacturing process from the starting materials up to the final dilution to be incorporated into the finished medicinal product must be fully described.
Wells with evidence of CPE are considered to be infected andneutralisation titres are expressed as the reciprocal of the final dilution of serum present in the serum/virus mixtures at the 50% end point estimated according to the Spearman-Karber method.
Ultomiris requires dilution to a final concentration of 5 mg/mL.
The final drug concentration after dilution is approximately 1.2 mg/mL.
After dilution, the final concentration of the solution to be infused is 5 mg/ml.
The concentration of the final solution after dilution should be either 4 micrograms/ml or 8 micrograms/ml.
Dilution to a final concentration<0.2 MIU.(2 µg) per ml is not recommended at any time.
Dilution to a final concentration less than 0.2 MU(2 µg) per mL is not recommended at any time.
Dilution to a final concentration< 0.2 MU/ml(2 μg/ml) is not recommended at any time.
Dilution to a final concentration less than 0.2 MU(2 µg) per mL is not recommended at any time.
Dilution to a final concentration less than 0.2 MU(2 µg) per mL is not recommended at any time.
Dilution to a final concentration< 0.2 MU/ml( 2?g/ml) is not recommended at any time.
Dilution to a final concentration less than 0.2 MIU(2 μ g) per ml is not recommended at any time.
The following table shall be used to obtain a final solution which, after appropriate dilution, will be within the measuring range for each method.