The damage over time component does stack with the glyph but additively.

這個DOT部分和銘文相疊而不是相加。

SPSS11.5 and excel statistical software were performed for the statistical analysis. 2. Experiment in vivo MRIgHIFU thermocoagulation was carried out in muscular tissues of rabbits. The parameters were power-250W and time-15s under the dot irradiating. MRI T-MAP was observed during treatment and the region size of adscendent temperature was measured (blue:45℃-50℃,green:50℃-55℃,yellow:55℃-60℃,red:60℃-100℃).Af-ter treatment, firstly, scan PD_tse and T2_tse, secondly, observe the changed signals of these images and measure the regions, finally, observe skin damage and measure the tissue necrosis.

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Aiming at the image to be captured is easy and intuitive, with the single click trigger that enables the Datalogic 5-dot aimer, marking the four corners and center of the reading area.

瞄準要捕捉的影像十分簡單而直觀，憑借啟用Datalogic 5 點瞄準器的單扣扳手，對讀取區(qū)域的四個角和中心定位又大又粗又长又硬好爽国产。

This article supposed a novel idea of building a new kind of database by unifying algebraical method and geometrical method. Each LssDNA was presented by a dot on a natural number coordinates axes, then the database was termed by'DotBank'.

該數據庫中的每一條LssDNA都與數軸上代表自然數的一個點相對應性插图真人无遮挡，因此將此類數據庫稱為&點庫&。

The detectable group, biotin-ε-aminocaproic acid N-hydroxysuccinimide ester, is attached to the remaining amino group. A series of multiamine compouds, i. e. ethylendiamine, 1, 6-hexandediamine, triethylenetetramine, tetraethylenepentamine, and synthetic polyarylamide are used inlabelling, it is found that linker arms and steric hindrance effect the detection sensitivity. The probes labeled by 1, 6-hexandediamine and triethylenetetramine can detect 0.1-0.5pg target DNA in dot blot hybridization, and their sensitivities are better than the others.

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The ELISA titre was 1:2000.By cell fusion, 46 hybridoma cell lines were screened,and 10 lines were cloned with limited dilution method.16 lines secreting anti-bFGF monoclonal antibody were been developed, and 2 lines targeted fusion protein. Sensitive ELISA and dot-ELISA for bFGF was developed with this mAb. The detection limit of them were 0.1 ng/well and 0.5 ng/well. The expression level of anti-bFGF mAb by different rebuilt engineering cells were identified by western blot and to direct rebuild recombiment engineering cell. The dose and character of anti-bFGF mAb inhibiting bFGF biology activity were searched by 3T3 cell line. Searching 20 tissue of liver cancer, liver cancer cell lines and general tissue of liver, finding bFGF were highly expressed in tissues of liver cancer and liver cancer cell lines. Affinity chromatography purifying bFGF was set up by mAb binging CNBr-pepharose 4B, and the purification was 95%. We found that the titer of anti-bFGF antibody was very high in serum of neuropathic amyotrophia.

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The website that taught oneself dot ASP is made arrived in company of a network dawdle, had held out those who mix actually, basically seeing you is quite argute, the technology is bad to have nothing to do with, there is a program to be able to download on the net, need to alter, oneself won't be OK consult at the same time, but cannot let them see your what does not understand.

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Dot and Southern blotting analysis of transgenic individuals resistant to herbicide Basta indicated that all of these individuals contained T-DNA insertion.

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In this study,an experimental modelwas developed and established with freshwater crayfish Cambarus clarkii to prolif-erate White Spot Syndrome Virusin vivo.The success and reliability ofthis model was confirmed by transmission electron microscopy,dot-blotand hybridization in situ etc.

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