Übersetzung für "Wieder aufgetaut" in Englisch

We'll be unfrozen as soon as we arrive.

We're asked which year we want to be alive again after the freezing.

The suspension was deep-frozen and re-thawed at 0° to +4° C.

It must merely be thawed again before use.

For this, the dispersion is cooled to -25° C., then thawed and filtered.

The reaction mixture was frozen and was degassed under reduced pressure, nitrogen was passed through and the mixture was thawed again.

Some time later the two are discovered by a team of researchers and are thawed by accident.

When the track is again unfrozen, all effects will be recalculated in real time.

As described in Example 1, this slurry that is now doped is subsequently frozen and re-thawed.

In the known cryopreservation biological samples are frozen while maintaining vitality and subsequently thawed out again as needed while maintaining vitality.

Personally, I think it's because the company tried to cryonically freeze him for a year... And then accidentally thawed him out a few days later.

In U.S. Pat. No. 4,081,431 a method is described for making a concentrate containing antihemophilic globulin A in addition to a prothrombin complex and a solution of stable serum proteins in which as starting material a frozen ion exchange plasma is used which is thawed again at temperatures between 2° and 8° C. and from which the supernatant plasma fluid is separated from the factor-VIII-containing protein and this cryoprecipitate processed in the known per se manner to a factor-VIII concentrate, while the plasma fluid is freed from the factors II, VII, IX and X by adsorption over commercial tricalcium phosphate, and then from the plasma fluid, over colloidal silica with a specific surface of 50 to 400 m2 /g, the still remaining coagulation factors and other unstable proteins are adsorbed and a solution of stable serum proteins remains behind.

The present invention relates to the treatment of bakery products to be stored in the deep frozen state, of the kind in which the actual products are deep frozen in an appropriate plant after the baking process and removed from the plant and thawed out again for the purpose of preparation for consumption.

In U.S. Pat. No. 4,081,431 a method is described for making a concentrate containing antihemophilic globulin A in addition to a prothrombin complex and a solution of stable serum proteins in which as starting material a frozen ion exchange plasma is used which is thawed again at temperatures between 2° and 8° C. and from which the supernatant plasma fluid is separated from the factor-VIII-containing protein and this cryoprecipitate processed in the known per se manner to a factor-VIII concentrate, while the plasma fluid is freed from the factors II, VII, IX and X by adsorption over commercial tricalcium phosphate, and then from the plasma fluid, over colloidal silica with a specific surface of 50 to 400 m2 /g, the still remaining coagulation factors and other unstable proteins are adsorbed and a solution of stable serum proteins remains behind.

In addition to the advantageous properties mentioned, it is particularly surprising that the concentrate also always remains homogeneous, even after it has been frozen for a prolonged time and then thawed.

During transportation or storage in the cold, the solutions thus gel and have to be thawed before the printing operation.

A method as set forth in claim 1, wherein, upon adding said protein precipitating agent in step (d), a suspension is obtained, which is frozen and re-thawed at a temperature of from about 0° C. to about 4° C., to obtain a supernatant, which is discarded, and a Factor-VIII-containing precipitate, said Factor VIII-containing precipitate is dissolved in a glycine-citrate-NaCl buffer solution in the presence of antithrombin III-heparinoid complex or antitnrombin III-heparin complex, and processed into stable form.

Quantities of approximately 50 g of the dispersion were introduced into 50 ml wide-necked bottles and frozen for about 16 hours at -5 to -10° C. and then thawed again for about 8 hours at room temperature (=1 cycle).

Following completion of polymerization, the dispersion is cooled to room temperature and frozen in order to obtain the polymerizate solid and thawed again in hot water (freezing coagulation).

The phosphodiesterase used was prepared by centrifugal extraction at 10,000 g from human blood platelets which were frozen in water and then thawed.

Parts of the first passage of HKC and of HFS are optionally frozen according to well-known methods at -70° C. or in liquid nitrogen, thawed when needed and subsequently used.

Preferably, the cells which are to be permeabilized by freezing and thawing are suspended in dilute buffer solution of pH 6 to 7 after they have been separated from the culture medium, and in this form they are frozen at about -20° C. and subsequently thawed at room temperature.

For this purpose, 100 ml of the developer were frozen for 24 hours at ?20° C. and then thawed again.

In freeze agglomeration, the dispersions are frozen in layers, producing partial colloidal instability which leads to clustering of the polymer dispersion particles, and are subsequently thawed.

Proteins such as antibodies tend to aggregate in the neutral pH range especially if the solutions are frozen (optionally lyophilized) once or several times and thawed again.

Upon operation of the filter unit, the medium is frozen and subsequently thawed again so that a volume expansion upon conversion from the liquid to the solid state of the medium occurs.