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The company owns the industry's most advanced product release suspended production line, set the beat automatically Tooling flip board production line equipment, such as five lines, at the same time, Germany also has a Wagner paint line; has advanced gas detection chamber, electrical testing room, equipped with advanced detection measurement, laboratory equipment, and rely on high-tech talent, to create a more technology-gas products, are sold in every region of the world.

公司拥有目前行业内最先进的悬挂式积放生产线、定节拍自动翻转工装板生产线等5条装备流水线,同时还配有德国瓦格纳喷涂线一条;拥有先进的燃气检测室、电器检测室,配备先进的检测测量、实验设备,并依托高科技人才,创造出更高技术的燃气产品,销售到全球每个地区。

The tests of heavy metals and residual pesticides in Radix Curcumae show that Cu,Cd,Hg,Pb and As as well as dichlorodiphenyl trichloroethane, benzene hexachloride, pentachloronitro benzene etc.

通过对2002年、2003年郁金GAP基地所产药材的重金属及砷盐和农药残留量的检测,确定采用适合药材检测、GAP认可的《药用植物及制剂进出口绿色行业标准》为检测依据和限量标准。

Methods Determine the marker of hepatitis B by ELISA, total protein by biuret method, albumin by bromocresol green method, and the component of serum protein by agarose gel electrophoresis.

采用酶联免疫吸附实验检测乙肝标志物,双缩脲法检测总蛋白,溴甲酚绿法检测白蛋白,琼脂糖凝胶电泳法分析血清蛋白组分。

Methods HPDLFs were primary cultured from tissue explants, and the cells of the 5th to 8th passages were used after immunohistochemical identification of keratin and vimentin expressions. The cells were divided into 5 groups and treated with TP at 1, 0.5, 0.25, 0.125, and 0.0625 mg/ml, respectively, with another group without TP treatment as the blank control group. Cell counting and MTT colorimetric assay were performed to assess the cell proliferation, and flow cytometry was employed to determine the DNA content of the HPDLFs.

采用组织块培养法培养原代人牙周膜成纤维细胞并传代,经免疫组化SABC法检测角蛋白和波形丝蛋白鉴定,取5~8代细胞用于实验;按茶多酚不同浓度分1mg/ml、0.5mg/ml、0.25mg/ml、0.125mg/ml、0.0625mg/ml组和空白对照组,采用细胞计数法、MTT法检测细胞增殖情况,流式细胞术检测细胞DNA含量。

Routine detecting techniquefor cell immunity such as white blood count and differential, lymphocyte blastogenesis test has beenused, and combine with flow cell technology to detect the level of cell immunization after advancedimmunization at several important aspect, and tracking experiments to observe changes in the numberof the WBC and lymphocytes, lymphocyte proliferation, the dynamic changes of CD4~+ and CD8~+lymphocyte subsets andγ-IFN; and detected dynamic changes rules of IgG, IgM in humor andmucosa with indirect ELISA, then compare with ordinary immunization methods.

主要采用白细胞计数和分类计数、淋巴细胞转化试验等常规细胞免疫检测技术结合先进的流式细胞技术从细胞免疫的几个重要方面入手检测猪瘟超前免疫后细胞免疫的水平,并进行跟踪试验,观察其白细胞、淋巴细胞数目变化情况,淋巴细胞增殖情况,CD~(4+)和CD~(8+)淋巴细胞亚群及γ-IFN的动态变化规律;同时通过间接ELISA方法检测体液和黏膜中各IgG、IgM的动态变化规律,同时与普通免疫方法进行比较。

The effects of temperature on the stability of measurement result and the initial BOD concentration on measurement time were investigated.

研究了温度对检测结果的影响,初始BOD浓度与检测时间的关系,并探讨了检测结果的重现性及其线性范围。

From sample treatment to data analysis of the detection, 30 minutes is enough to complete the whole detection process, providing a new on site detection method for Brucella.

整个检测过程,从样品处理到数据分析,能够在30分钟内完成,从而实现了布鲁氏菌的现场快速检测,为布鲁氏菌的现场快速检测提供了一种新的方法。

Methods The experimental TBI model was established by bumpiness of free falling body according to Feeney′s.The rats′cerebral edema were imaged with magnetic resonance image,The changes of brain water content and permeability of blood-brain barrier were measured by the methods of wet and dry weight and Evans blue fluorometry.The expression of AQP-4 mRNA was examined by reverse transcriptase polymerase chain reaction.

按照改进的Feeney自由落体撞击法建立大鼠创伤性脑损伤模型,用磁共振成像对大鼠脑水肿进行检测,干/湿比重法和伊文思蓝测定法观察大鼠TBI后不同时相脑组织含水量和BBB通透性的变化,并采用逆转录聚合酶链反应法检测AQP-4 mRNA的表达,蛋白质免疫印迹法检测AQP-4蛋白的表达。

The expressions of HO-1 and HO-2 mRNA were detected using reverse transcription polymerase chain and the relative amount of CO released into the media was quantitated as carboxyhemoglobin by enzyme linked immunosorbent assay.

通过逆转录聚合酶链式反应和免疫细胞化学法检测HO-1、HO-2 mRNA和蛋白的表达,酶联免疫法检测培养上清液中碳氧血红蛋白含量,四唑氮比色法检测细胞增殖。

Eleven QTLs were detected by the soft WinQTL Cartographer 2.0, which tow each were located on chromosomes 1, 5, 7, and 12 and one each on the chromosomes 2, 8 and 11. The phenotypic variation for leaf rolling degree explained by these QTLs ranged from 4.7% to 11.8%.

应用WinQTL Cartographer 2.0软件,共检测到11个抗旱QTL,分别位于第1,2,5,7,8,11,12染色体上,其中第1,5,7,12染色体每条上检测剑2个QTL,其余染色体上检测到1个QTL。

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