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METHOD AND SYSTEM FOR PREPARING tissue samples for histological and pathological examination

机译:制备用于组织学和病理学检查的组织样品的方法和系统

摘要

1.method for freezing of biochemically active tissue and frozen tissue sample includes immersion cooling environment, u0446u0438u0440u043au0443u043b u0438u0440u043eu0432u0430u043du0438u0435 cooling environment around the sample tissue in essentially u043fu043eu0441u0442u043eu00a0u043du043du043eu0439 specified speed and temperature u0434u043bu00a0 u0437u0430u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u00a0 sample tissue soto u0432u0438u0442u0440u0438u0444u0438u0446u0438u0440u043eu0432u0430u043bu0441u00a0 tissue sample and the tissue sample u0441u043eu0445u0440u0430u043du00a0u0435u0442 its u0430u043du0430u0442u043eu043cu0438u0447u0435u0441u043au0443u044e structure and u043eu0441u0442u0430u0435u0442u0441u00a0 biochemically active after u0440u0430u0437u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u00a0, time u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u0435 samples of tissue and study u0440u0430u0437u043cu043eu0440u043eu0436u0435u043du043du043eu0433u043e sample tissue.;2. method for preparing 1, further an outlet sample tissue.;3. method for 1, in which the study sample u0440u0430u0437u043cu043eu0440u043eu0436u0435u043du043du043eu0439 tissue includes a histological study.;4. method for 1, in which the study u0440u0430u0437u043cu043eu0440u043eu0436u0435u043du043du043eu0433u043e sample tissue includes u0443u043bu044cu0442u0440u0430u0441u0442u0440u0443u043au0442u0443u0440u043du043eu0435 study.;5. method for 1, in which the study includes the use of u0438u043cu043cu0443u043du043eu0433u0438u0441u0442u043eu0445u0438u043cu0438u0447u0435u0441u043au043eu0433u043e u0438u0441u0441u043bu0435u0434u043eu0432u0430u043du0438u00a0.;6. way to p.5, which includes fluorescent antibodies in immunohistochemistry staining.;7. method for 1, in which more than about 55 per cent of the sample tissue showed a lack of anatomical damage of cellular structure and u043eu0441u0442u0430u044eu0442u0441u00a0 biochemically active after the u0440u0430u0437u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u00a0.;8. method for 1, in which more than about 45 per cent of the sample tissue showed a lack of u043fu043eu0432u0440u0435u0436u0434u0435u043du0438u00a0 cell anatomical structure and u043eu0441u0442u0430u044eu0442u0441u00a0 biochemically active after the u0440u0430u0437u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u00a0.;9. method for 1, in which more than about 85 per cent of the sample tissue u0441u043eu0445u0440u0430u043du00a0u044eu0442 its u0430u043du0430u0442u043eu043cu0438u0447u0435u0441u043au0443u044e structure and u043eu0441u0442u0430u044eu0442u0441u00a0 intact after u0440u0430u0437u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u00a0.;10. method for 1, in which the cooling environment support at a temperature of from about - 20 degrees to about 30 degrees u0446u0435u043bu044cu0441u0438u00a0 u0446u0435u043bu044cu0441u0438u00a0.;11. method for 1, in which the speed of cooling environment around the sample tissue u0441u043eu0441u0442u0430u0432u043bu00a0u0435u0442 around 35 liters per minute on foot cooling environment in area not more than employment about 24 inches in width, and 48 inches in depth.;12. method for 1, in which the coolant circulating through the engine, and the node with the environment u043au0440u044bu043bu044cu0447u0430u0442u043au043eu0439, steeped in the cooling environment.;13. method for u0446u0438u0440u043au0443u043bu0438u0440u043eu0432u0430u043du0438u0435 1, further a cooling environment around u043cu043du043eu0433u043eu0437u0430u0445u043eu0434u043du043eu0433u043e coils attached to the heat exchanger, steeped in the cooling environment serpentine heat exchanger capable of u0443u0434u0430u043bu00a0u0442u044c, with at least the same amount of heat from the cooling environment, a u043eu0445u043bu0430u0436u0434u0430u044eu0449u0430u00a0 wednesday u0443u0434u0430u043bu00a0u0435u0442 of sample tissue.;14.method of preparing tissue samples u0434u043bu00a0 u0438u0441u043fu043eu043bu044cu0437u043eu0432u0430u043du0438u00a0 u0434u043bu00a0 u0438u0441u0441u043bu0435u0434u043eu0432u0430u043du0438u00a0 by immersion of the biologically active tissue in the cooling medium have, and direct freezing of tissue to a temperature greater than about 30 degrees u0446u0435u043bu044cu0441u0438u00a0 by u0446u0438u0440u043au0443u043bu0438u0440u043eu0432u0430u043du0438u00a0 cooling environment around the u0437u0446u0430 tissue, with essentially u043fu043eu0441u0442u043eu00a0u043du043du043eu0439 specified speed and temperature,what u0432u0438u0442u0440u0438u0444u0438u0446u0438u0440u0443u0435u0442u0441u00a0 tissue sample, the tissue sample u0430u043du0430u0442u043eu043cu0438u0447u0435u0441u043au0443u044e maintains its structure and u043eu0441u0442u0430u0435u0442u0441u00a0 biochemically active after u0440u0430u0437u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u00a0.;15. method for preparing on p.14, further cuts the sample tissue.;16. a way to question 14, further providing some samples of tissue.;17. a way to question 14, in which the study includes histological study.;18. a study on p.14, which includes u0443u043bu044cu0442u0440u0430u0441u0442u0440u0443u043au0442u0443u0440u043du043eu0435 study.;19. a study on p.14, which includes the use of u0438u043cu043cu0443u043du043eu0433u0438u0441u0442u043eu0445u0438u043cu0438u0447u0435u0441u043au043eu0433u043e u0438u0441u0441u043bu0435u0434u043eu0432u0430u043du0438u00a0.;20. way on p.19, which includes fluorescent antibodies in immunohistochemistry staining.;21. a way to question 14, in which more than 40 per cent of the sample tissue u0441u043eu0445u0440u0430u043du00a0u0435u0442 its u0430u043du0430u0442u043eu043cu0438u0447u0435u0441u043au0443u044e structure and u043eu0441u0442u0430u0435u0442u0441u00a0 biochemically active after u0440u0430u0437u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u00a0.;22. a way to question 14, in which more than 80 per cent of the sample tissue u0441u043eu0445u0440u0430u043du00a0u0435u0442 its u0430u043du0430u0442u043eu043cu0438u0447u0435u0441u043au0443u044e structure and u043eu0441u0442u0430u0435u0442u0441u00a0 biochemically active after u0440u0430u0437u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u00a0.;23. a way to question 14, in which more than about 85 per cent of the sample tissue u0441u043eu0445u0440u0430u043du00a0u0435u0442 its u0430u043du0430u0442u043eu043cu0438u0447u0435u0441u043au0443u044e structure and u043eu0441u0442u0430u0435u0442u0441u00a0 intact after u0440u0430u0437u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u00a0.;24. a way to question 14, in which the cooling environment support at a temperature of about 20 degrees to about 30 degrees u0446u0435u043bu044cu0441u0438u00a0 u0446u0435u043bu044cu0441u0438u00a0.;25. a way to question 14, in which the speed of cooling environment around the sample tissue u0441u043eu0441u0442u0430u0432u043bu00a0u0435u0442 around 35 liters per minute on foot cooling environment through the area of no more than an eye luo 24 inches in width, and 48 inches in depth.;26. a way to question 14, in which the coolant circulating through the engine, and the node with the environment u043au0440u044bu043bu044cu0447u0430u0442u043au043eu0439, steeped in the cooling environment.;27. method for u0446u0438u0440u043au0443u043bu0438u0440u043eu0432u0430u043du0438u0435 p.14, further a cooling environment around u043cu043du043eu0433u043eu0437u0430u0445u043eu0434u043du043eu0433u043e coils attached to the heat exchanger, steeped in the cooling medium serpentine heat exchanger capable of u0443u0434u0430u043bu00a0u0442u044c, with at least the same amount of heat from the cooling environment, a u043eu0445u043bu0430u0436u0434u0430u044eu0449u0430u00a0 wednesday u0443u0434u0430u043bu00a0u0435u0442 of sample a swatch and.;28.the system u0434u043bu00a0 u0438u0441u043fu043eu043bu044cu0437u043eu0432u0430u043du0438u00a0 during preparation of sample tissue u0434u043bu00a0 u0438u0441u0441u043bu0435u0434u043eu0432u0430u043du0438u00a0, u0441u043eu0434u0435u0440u0436u0430u0449u0430u00a0 reservoir with a cooling medium, is the possibility of receiving u043eu0431u0440u0430u0437u0446 a biochemically active tissue u0434u043bu00a0 u043fu043eu0433u0440u0443u0436u0435u043du0438u00a0 in cooling environment, one or more devices u0434u043bu00a0 u0446u0438u0440u043au0443u043bu00a0u0446u0438u0438 cooling environment of u0434u043bu00a0 u0446u0438u0440u043au0443u043bu0438u0440u043eu0432u0430u043du0438u00a0 decree anna cooling environment.coil heat exchanger u0434u043bu00a0 u0443u0434u0430u043bu0435u043du0438u00a0 heat from the cooling environment, freeze the knot by the heat of the heat exchange coils attached to u0434u043bu00a0 u0443u0434u0430u043bu0435u043du0438u00a0 nick and the reservoir u0434u043bu00a0 cooling environment, the one or more u0446u0438u0440u043au0443u043bu00a0u0446u0438u043eu043du043du044bu0445 device and the node are not u0434u043bu00a0 freeze a u0437u0430u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u00a0 sample tissue temperatures higher.what about - 30 degrees u0446u0435u043bu044cu0441u0438u00a0 by u0446u0438u0440u043au0443u043bu0438u0440u043eu0432u0430u043du0438u00a0 cooling environment around the sample tissue, essentially u043fu043eu0441u0442u043eu00a0u043du043du043eu0439 a given speed and temperature so that u0440u0430u0437u0435u0446 u0432u0438u0442u0440u0438u0444u0438u0446u0438u0440u0443u0435u0442u0441u00a0 tissue, the tissue sample u0441u043eu0445u0440u0430u043du00a0u0435u0442 its u0430u043du0430u0442u043eu043cu0438u0447u0435u0441u043au0443u044e structure and u043eu0441u0442u0430u0435u0442u0441u00a0 biochemically active after u0440u0430u0437u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u00a0.;29. system, p.28, in which the study includes histological study.;30. the system includes u0443u043bu044cu0442u0440u0430u0441u0442u0440u0443u043au0442u0443u0440u043du043eu0435 p.28, in which the research study.;31. system, p.28, in which the study includes the use of u0438u043cu043cu0443u043du043eu0433u0438u0441u0442u043eu0445u0438u043cu0438u0447u0435u0441u043au043eu0433u043e u0438u0441u0441u043bu0435u0434u043eu0432u0430u043du0438u00a0.;32. the system includes p.31 in which immunohistochemistry staining fluorescent marked antibodies.;33. system, p.28, in which more than 40 per cent of the sample tissue u0441u043eu0445u0440u0430u043du00a0u0435u0442 its u0430u043du0430u0442u043eu043cu0438u0447u0435u0441u043au0443u044e structure and u043eu0441u0442u0430u0435u0442u0441u00a0 biochemically active after u0440u0430u0437u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u00a0.;34. system, p.28, where more than 80 per cent of the sample tissue u0441u043eu0445u0440u0430u043du00a0u0435u0442 its u0430u043du0430u0442u043eu043cu0438u0447u0435u0441u043au0443u044e structure and u043eu0441u0442u0430u0435u0442u0441u00a0 biochemically active after u0440u0430u0437u043cu043eu0440u0430u0436u0438u0432u0430u043du0438u00a0.;35. system, p.28, in which more than about 85 per cent of the sample tissue u0441u043eu0445u0440u0430u043du00a0u0435u0442 its u0430u043du0430u0442u043eu043cu0438u0447u0435u0441u043au0443u044e structure and u043eu0441u0442u0430u0435u0442u0441u00a0 intact.;36. system, p.28, in which cooling environment support at a temperature from about 20 to about 30 degrees u0446u0435u043bu044cu0441u0438u00a0.;37. system, p.28, in which the speed of cooling environment around the sample tissue u0441u043eu0441u0442u0430u0432u043bu00a0u0435u0442 around 35 liters per minute on foot cooling environment in area not more than okay. are 24 inches in width, and 48 inches in depth.;38. system, device u043fu0440u0435u0434u0441u0442u0430u0432u043bu00a0u0435u0442 u0446u0438u0440u043au0443u043bu00a0u0446u0438u043eu043du043du043eu0435 p.28, in which a node with an engine and u043au0440u044bu043bu044cu0447u0430u0442u043au043eu0439, immersed in a cooling environment.;39. system, p.28, in which coolant circulating around the heat exchanger coils attached to the environment u043cu043du043eu0433u043eu0437u0430u0445u043eu0434u043du043eu0433u043e, steeped in the cooling environment, and the coil u0442u0435u043fu043bu043eu043eu0431u043c u0443u0434u0430u043bu00a0u0442u044c u0435u043du043du0438u043au0430 capable of at least the same amount of heat from the cooling environment, a u043eu0445u043bu0430u0436u0434u0430u044eu0449u0430u00a0 wednesday u0443u0434u0430u043bu00a0u0435u0442 of sample tissue.
机译:1.用于冷冻生化活性组织的方法,冷冻组织样品包括浸没冷却环境, u0446 u0438 u0440 u043a u0443 u043b u0438 u0440 u043e u0432 u04330 u043d u0438 u0435周围的冷却环境样本组织基本上位于 u043f u043e u0441 u0442 u043e u00a0 u043d u043d u043e u0439指定的速度和温度 u0434 u043b u00a0 u0437 u0430 u043c u043c u043e u0440 u0430 u0436 u0438 u0432 u0430 u043d u0438 u00a0样本组织sou u0432 u0438 u0442 u0440 u0438 u0444 u0438 u0446 u0438 u0440 u043e u0432 u0430 u0430 u043b u0441 u00a0组织样本和组织样本 u0441 u043e u0445 u0440 u0430 u043d u00a0 u0435 u0442其 u0430 u043d u0430 u0442 u0432 u043e u043c u0438 u0447 u0435 u0435 u0441 u043a u0443 u044e结构和 u043e u0441 u0442 u0430 u0435 u0442 u0441 u00a0在 u0440 u0430 u0437 u043c u043e u0440 u0430 u0436 u0438 u0432 u0432 u0430 u043d u0438 u00a0,时间 u043后具有生化活性u043e u0440 u0430 u0436 u0438 u0432 u0430 u043d u0438 u0435示例组织和研究的样本组织 u0440 u0430 u0437 u043c u043e u0440 u043e u0436 u0435 u043d u043d u043e u0433 u043e u043e 1,进一步制备出口样品组织的方法;; 3。 1的方​​法,其中研究样本 u0440 u0430 u0437 u043c u043e u0440 u043e u0436 u0435 u043d u043d u043e u0439组织包括组织学研究; 4。 1的方​​法,其中研究 u0440 u0430 u0437 u043c u043e u0440 u043e u0436 u0435 u043d u043d u043e u0433 u043e样本组织包括 u0443 u043b u043b u044c u0442 u0440 u0430 u0441 u0442 u0440 u0443 u043a u0442 u0443 u0440 u043d u043e u0435研究; 5。 1的方​​法,其中研究包括使用 u0438 u043c u043c u0443 u043d u043e u0433 u0438 u0441 u0442 u043e u0445 u0438 u043c u0438 u0447 u0447 u0435 u0441 u043a u043e u0433 u043e u0438 u0441 u0441 u043b u0435 u0434 u043e u0432 u0430 u043d u0438 u00a0。; 6。 p.5的方法,其在免疫组织化学染色中包括荧光抗体; 7。 1的方​​法,其中超过约55%的样本组织显示出对细胞结构的解剖学损害,并且在 u0440 u0430之后具有生化活性。 u043e u0441 u0442 u0430 u044e u0442 u0441 u00a0 u0437 u043c u043e u0440 u0430 u0436 u0438 u0432 u0430 u043d u0438 u00a0。; 8。 1的方​​法,其中约有45%以上的样本组织显示缺少 u043f u043e u0432 u0440 u0435 u0436 u0434 u0435 u043d u0438 u00a0细胞解剖结构和 u043e u0441 u0442 u0430 u044e u0442 u0441 u00a0在 u0440 u0430 u0437 u043c u043e u0440 u0430 u0436 u0438 u0432 u0430 u043d u0438 u00a0.9之后具有生化活性。 1的方​​法,其中约有85%的样本组织 u0441 u043e u0445 u0440 u0430 u043d u00a0 u044e u0442其 u0430 u043d u0430 u0442 u043e u043c u043c u0438 u0447 u0435 u0441 u043a u0443 u044e结构和 u043e u0441 u0442 u0430 u044e u0442 u0441 u0441 u00a0完好保存 u0440 u0430 u0437 u043c u043c u043e u0440 u0430 u0436 0 u0432 u0430 u043d u0438 u00a0。; 10。 1的方​​法,其中冷却环境在大约-20度到大约30度的温度下支撑 u0446 u0435 u043b u043c u044c u0441 u0438 u00a0 u0446 u0435 u043b u044c u0441 u0438 u00a0。; 11。 1的方​​法,其中样品组织周围的冷却环境的速度以每分钟35升左右的速度在不超过就业的面积上以每分钟35升的速度围绕周围的样本组织 u0441 u043e u0441 u0442 u0430 u0432 u043b u00b0宽度约24英寸,深度约48英寸; 12。 1的方​​法,其中冷却液循环通过发动机,并且节点与环境 u043a u0440 u044b u043b u044c u0447 u0430 u0442 u043a u043e u0439浸在冷却环境中。; 13 。 u0446 u0438 u0440 u043a u0443 u043b u0438 u0440 u043e u0432 u0430 u043d u0438 u0435 1的方法,进一步围绕 u043c u043d u043d u043e u0433 u043e u0437 连接到热交换器的u0430 u0445 u043e u0434 u043d u043e u0433 u043e线圈浸入冷却环境中的蛇形热交换器中,该蛇形热交换器具有 u0443 u0434 u0430 u043b u00a0 u0442 u044c,至少来自制冷环境的相同热量,样品 u043e u0445 u043b u0430 u0436 u0434 u0430 u044e u0449 u0430 u00a0周三 u0443 u0434 u0430 u043b u043b u00a0 u0435 u0442 14.组织样本的制备方法 u0434 u043b u00a0 u0438 u0441 u043f u043e u043b u044c u0437 u043e u043e u0432 u0430 u043d u0438 u00a0 u043a u0434 u043b u00a0 u0438通过将生物活性组织浸入冷却介质中,并将组织直接冷冻到大于约30度的温度,从而将组织冷冻 u0435 u043b u044c u0441 u0438 u00a0 by u0446 u0438 u0440 u043a u0443 u043b u0438 u0440 u043e u0432 u0430 u043d u0438 u00a0围绕 u0437 u0446 u0430组织的冷却环境,基本上是 u043f u043e u0441 u0442 u043e u00a0 u043d u043d u043e u0439指定的速度和温度,什么 u0432 u0438 u0442 u0440 u0438 u0444 u0438 u0446 u0438 u0440 u0443 u0435 u0442 u0441 u00a0组织样本,组织样本 u0430 u043d u0430 u0442 u043e u043c u0438 u0447 u0435 u0441 u043a u0443 u044e保持其结构,并且在 u0440 u0430 u0437 u043c u043e u0440之后具有生化活性u0430 u0436 u0438 u0432 u0430 u043d u0438 u00a0。; 15。第14页的制备方法,还可以切割样品组织。; 16。问题14的方法,进一步提供了一些组织样本; 17。问题14的方法,其中的研究包括组织学研究; 18。关于p.14的研究,其中包括 u0443 u043b u044c u0442 u0440 u0430 u0441 u0442 u0440 u0443 u043a u0442 u0443 u0440 u043d u043e u0435研究。19。关于第14页的研究,其中包括使用 u0438 u043c u043c u0443 u043d u043e u0433 u0438 u0441 u0442 u043e u0445 u0438 u043c u0438 u0447 u0447 u0435 u0441 u043a u043e u0433 u043e u0438 u0441 u0441 u043b u0435 u0434 u043e u0432 u0430 u043d u0438 u00a0。; 20。 p.19的方法,其中包括免疫组织化学染色中的荧光抗体。; 21。问题14的方法,其中40%以上的样本组织 u0441 u043e u0445 u0440 u0430 u043d u00a0 u0435 u0442其 u0430 u043d u0430 u0442 u043e u043c u043c u0438 u0447 u0435 u0441 u043a u0443 u044e结构和 u043e u0441 u0442 u0430 u0435 u0442 u0441 u0441 u00a0在 u0440 u0430 u0437 u043c u043e u0440 u0430 u0430 u0436后具有生化活性u0438 u0432 u0430 u043d u0438 u00a0。; 22。问题14的方法,其中80%以上的样本组织 u0441 u043e u0445 u0440 u0430 u043d u00a0 u0435 u0442其 u0430 u043d u0430 u0442 u043e u043c u043c u0438 u0447 u0435 u0441 u043a u0443 u044e结构和 u043e u0441 u0442 u0430 u0435 u0442 u0441 u0441 u00a0在 u0440 u0430 u0437 u043c u043e u0440 u0430 u0430 u0436后具有生化活性u0438 u0432 u0430 u043d u0438 u00a0。; 23。问题14的方法,其中约有85%以上的样本组织为 u0430 u043d u0430 u0442 u043e u043c u041 u043e u0445 u0440 u0430 u043d u00a0 u0435 u0442 u0438 u0447 u0435 u0441 u043a u0443 u044e结构和 u043e u0441 u0442 u0430 u0435 u0442 u0441 u00a0完整保留 u0440 u0430 u0437 u043c u043e u0440 u0430 u0 u0438 u0432 u0430 u043d u0438 u00a0。; 24。问题14的一种方法,其中冷却环境在大约20度到大约30度的温度下支撑 u0446 u0435 u043b u044c u0441 u0438 u00a0 u0446 u0435 u043b u044c u0441 u0438 u00a0。; 25。问题14的一种方法,其中样品组织周围的冷却环境的速度在每分钟35英尺的步行冷却环境中穿过样品区域周围的速度大约为每分钟35升。宽度不超过24英寸,深度不超过48英寸的眼睛; 26。问题14的方法,其中冷却剂循环通过发动机,并且节点与环境 u043a u0440 u044b u043b u044c u0447 u0430 u0442 u043a u043e u0439浸在冷却环境中。 ; 27。 u0446 u0438 u0440 u043a u0443 u043b u0438 u0440 u043e u0432 u0430 u043d u0438 u0435 p.14的方法,进一步在 u043c u043d u043e u043e u0433 u043e u0437 u0430 u0445 u043e u0434 u043d u043e u0433 u043e盘管已浸入冷却介质蛇形换热器中,该盘管可以安装在 u0443 u0434 u0430 u043b u00a0 u0442 u044c u043e u0445 u043b u0430 u0436 u0434 u0430 u044e u0449 u0430 u00a0周三 u0443 u0434 u0430 u043b u00a0 u0435 u0442样本样本; 28。在准备样本组织期间,系统 u0434 u043b u00a0 u0438 u0441 u043f u043e u043e u043b u044c u0437 u043e u043e u0432 u0430 u043d u0438 u00a0 u043b u00a0 u0438 u0441 u0441 u043b u0435 u0434 u043e u0432 u0430 u043d u0438 u00a0, u0441 u043e u0434 u0435 u0435 u0440 u0436 u0430 u0449 u0430 u0430带有冷却介质的情况下,有可能接受 u043e u0431 u0440 u0430 u0437 u0446生化试剂散热环境中的医用活性组织 u0434 u043b u00a0 u043f u043e u0433 u0440 u0443 u0436 u0435 u043d u0438 u00a0,一个或多个设备 u0434 u043b u00a0 u0446 u0438 u0440 u043a u0443 u043b u00a0 u0446 u0438 u0438 u0434 u043b u00a0 u0446 u0438 u0440 u043a u0443 u043b u0438 u0440 u0440 u043e u0432 u0430 u043d u0438的冷却环境根据冷却环境的规定。盘管热交换器 u0434 u043b u00a0 u0443 u0434 u0430 u043b u0435 u043d u0438 u00a0来自冷却环境的热量,通过连接到的热交换盘管的热量冻结结。 u0434 u043b u00a0 u0443 u0434 u0430 u043b u0435 u043d u0438 u00a0缺口和储存器 u0434 u043b u00a0冷却环境,则一个或多个 u0446 u0438 u0440 u043a u0443 u043b u00a0 u0446 u0438 u043e u043d u043d u044b u0445设备和该节点不是 u0434 u043b u00a0冻结 u0437 u0430 u043c u043e u0440 u0430 u0436 u0438 u0432 u0430 u043d u0438 u00a0样本组织温度更高-大约-30度 u0446 u0435 u043b u044c u0441 u0438 u00a0通过 u0446 u0438 u0440 u043a u0443 u043b u0438 u0440 u043e u0432 u0430 u043d u0438 u00a0样品组织周围的冷却环境,基本上是 u043f u043e u0441 u0442 u0442 u043e u00a0 u043d u043d u043e u0439给定的速度和温度,以便 u0440 u0430 u0437 u0435 u0446 u0432 u0438 u0442 u0440 u0438 u0444 u0438 u0446 u0438 u0440 u0443 u0435 u0442 u0441 u00a0组织,组织样本 u0441 u043e u0445 u0440 u0430 u043d u00a0 u0435 u0442其u0430 u043d u0430 u0442 u043e u043c u0438 u0447 u0447 u0435 u0441 u043a u0443 u0440 u0430 u0437 u043c u043e u0440 u04之后,u044e的结构和 u043e u0441 u0442 u0430 u0435 u0442 u0441 u00a0具有生化活性30 u0436 u0438 u0432 u0430 u043d u0438 u00a0。; 29。系统,第28页,其中研究包括组织学研究; 30。该系统包括 u0443 u043b u044c u0442 u0440 u0430 u0441 u0442 u0440 u0443 u043a u0442 u0443 u0440 u043d u043e u0435 p.28,在其中进行研究。31。系统,第28页,其中研究包括使用 u0438 u043c u043c u0443 u043d u043e u0433 u0438 u0441 u0442 u043e u0445 u0438 u043c u0438 u0447 u04447 u0435 u0441 u043a u043e u0433 u043e u0438 u0441 u0441 u043b u0435 u0434 u043e u0432 u0430 u043d u0438 u00a0。; 32。该系统包括p.31,其中免疫组织化学染色了荧光标记的抗体。; 33。系统,第28页,其中40%以上的样本组织 u0441 u043e u0445 u0440 u0430 u043d u00a0 u0435 u0442其 u0430 u043d u0430 u0442 u043e u043e u043c u0438 u0447 u0435 u0441 u043a u0443 u044e结构和 u043e u0441 u0442 u0430 u0435 u0442 u0441 u0441 u00a0在 u0440 u0430 u0437 u043c u043e u0440 u0430 u0430 u0436后具有生化活性u0438 u0432 u0430 u043d u0438 u00a0。; 34。系统,第28页,其中80%以上的样本组织 u0441 u043e u0445 u0440 u0430 u043d u00a0 u0435 u0442其 u0430 u043d u0430 u0442 u043e u043c u043c u0438 u0447 u0435 u0441 u043a u0443 u044e结构和 u043e u0441 u0442 u0430 u0435 u0442 u0441 u0441 u00a0在 u0440 u0430 u0437 u043c u043e u0440 u0430 u04436 u0432 u0430 u043d u0438 u00a0。; 35。系统,第28页,其中约有百分之八十五的样本组织 u0441 u043e u0445 u0440 u0430 u043d u00a0 u0435 u0442其 u0430 u043d u0430 u0442 u0432 u043e u043c u0438 u0447 u0435 u0441 u043a u0443 u044e结构和 u043e u0441 u0442 u0430 u0435 u0442 u0441 u00a0完整。; 36。系统,第28页,其中冷却环境支持的温度范围为大约20到大约30度。37。系统,第28页,其中样品组织周围的冷却环境的速度每分钟35升,步行区域附近的样品组织周围的冷却环境的速度不超过每分钟35升。比还好。宽24英寸,深48英寸; 38。系统,设备 u043f u0440 u0435 u0434 u0441 u0442 u0430 u0432 u043b u00a0 u0435 u0442 u0446 u0438 u0440 u043a u0443 u0433 u043b u00a0 u0446 u0438 u043e u043e u043d u043e u0435第28页,其中具有引擎和 u043a u0440 u044b u043b u044b u044c u0447 u0430 u0442 u043a u043e u043e u0439的节点浸没在冷却环境中。39。系统,第28页,其中冷却液在与环境相连的热交换器盘管周围循环 u043c u043d u043e u0433 u043e u0437 u0430 u0445 u043e u0434 u043d u043e u0433 u043e冷却环境,并具有线圈 u0442 u0435 u043f u043b u043e u043e u0431 u043c u0443 u0434 u0430 u043b u00a0 u0442 u044c u0435 u0435 u043d u043d u043d u0438 u043a u043a u0430 u043e u0445 u043b u0430 u0436 u0434 u0430 u044e u0449 u0430 u00a0周三 u0443 u0434 u0430 u0430 u043b u00a0 u0435 u0442的样本组织。

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