放射自显影的

And thaw, and cell fusion; Understanding the principles and operation procedures for autoradiograph; Mastering the skills of writing experiment reports and graphic drawing under microscope.

本课程是农业与生物学院本科学生的一门实验课程，本课程主要内容包括：掌握和了解普通光学显微镜、几种特殊显微镜和电镜的一般原理和使用方法；掌握显微镜临时标本的制备，会进行显微测量、细胞计数和染色体观察；初步观察细胞生理现象、细胞化学成分显示、染色体标本制备；掌握细胞培养、细胞冻存与复苏、细胞融合等技术的原理和方法；了解细胞放射自显影技术的原理和操作步骤；掌握实验报告的书写和镜下绘图的技能。

Protease treatment of the plasma membranes could abolish the binding but NaIO_4 and glycosidase could not, indicating that nsLTP144 bound to plasma membranes protein without carbohydrate moiety. Using the homobifunctional cross-linking regent bissuberate (BS~3) and rice plasma membranes incubated with ~(125)I-Trx-nsLTP144, we identified, after SDS-polyacrylamide gel electrophoresis and autoradiography, a putative protein receptor on the rice plasma membranes with the molecular mass around 60 kDa. NsLTP144 can not trigger extracelluar alkalization in arabidopsis, but can abolish the extracellular alkalization effect of phytopathogen elicitor cryptogein, suggesting that cryptogein and nsLTP144 may bind to the same membrane protein. In vitro pull-down assay showed that nsLTP144 interacted with OsCaM1, a possible extracellular calmodulin, implying that nsLTP144 and OsCaM1 could function in the same signal transduction pathway. These results shed light on revealing the roles of nsLTP in vivo and make it promising to finally characterize the plasma membranes receptor of nsLTP.

发现~(125)I-Trx-nsLTP144、~(125)I-Trx-nsLTP110与水稻细胞质膜均具有特异性结合，而且结合是饱和性的、可被竞争的，符合配体-受体结合的典型特征，同时用于对照实验的蛋白质~(125)I-Thioredoxin没有此特性，表明水稻细胞质膜上存在nsLTP的受体；利用可氧化糖基的NaIO_4和水解糖基的N\'-糖苷酶F处理水稻细胞质膜，再进行结合实验，结合活性几乎不受影响；而利用胰蛋白酶处理细胞膜则使得结合能力几乎完全丧失，表明其受体为没有经过糖基化修饰的蛋白质；利用交联剂BS~3交联配体一受体后，再进行SDS-PAGE分离和放射自显影，结果显示水稻细胞质膜上的nsLTP受体中有一个60kDa的蛋白质可以与nsLTP144发生特异性的结合，可能是其受体；细胞外碱化实验表明，nsLTP144不能促使拟南芥原生质体细胞培养液的细胞外碱化反应，却能猝灭来自植物病原菌的激发子Cryptogein刺激拟南芥原生质体产生的细胞外碱化反应，表明nsLTP和Cryptogein结合细胞膜上相同的位点，保护了植物细胞免受Cryptogein导致的细胞程序性死亡，并诱导系统获得性抗性的产生；体外Pull-down实验表明，nsLTP144和水稻的OsCaM1具有相互作用，暗示了nsLTP144和OsCaM1可能同在一个信号通路上起作用。

By using the "mechanical wounding"experimental system estabilished by us, and light- and electron microscopy, autoradiography and radioisotope technique, immuno-fluorescence localization, homologous clone and RACE technique, in situ mRNA hybridization and ELISA et al., we investigated the relationship between the transportation of exogenous JA and the secondary laticifer differentiation, the relationship between the producton and accumulation of endogenous JA and the laticifer differentiation from cambia, and the effect of appling exogenous jasmonates on the natural rubber production.

利用我们建立的机械伤害诱导乳管分化的实验系统，采用光学显微镜和电子显微镜技术、同位素示踪和放射自显影技术、免疫荧光定位技术、同源克隆和RACE技术、mRNA原位杂交和ELISA等技术，研究了外源茉莉酸在橡胶树体内的移动及其对维管形成层分化次生乳管的诱导效应、内源茉莉酸与乳管分化的关系以及茉莉酸类物质对天然橡胶产量的影响。

The protocol is summarized in Figure 18.16. A radioactive probe representing a gene (most often a labeled cDNA clone derived from the mRNA) is hybridized with thedenatured DNA of the polytene chromosomes in situ. Autoradiography identifies the position or positions of the corresponding genes by the superimposition of grains at a particular band or bands.

如图26.15所示为此过程草图：一个放射性探针代表一个基因（常是一个从mRNA中克隆得到的cDNA），它与原位多线染色体的变性DNA杂交，放射自显影仪可通过叠印特定纹带的纹理来识别应答基因的位置。

The protocol is summarized in Figure 18.16. A radioactive probe representing a gene (most often a labeled cDNA clone derived from the mRNA) is hybridized withthe denatured DNA of the polytene chromosomes in situ. Autoradiography identifies the position or positions of the corresponding genes by the superimposition of grains at a particular band or bands.

如图26.15所示为此过程草图：一个放射性探针代表一个基因（常是一个从mRNA中克隆得到的cDNA），它与原位多线染色体的变性DNA杂交，放射自显影仪可通过叠印特定纹带的纹理来识别应答基因的位置。

With Death guitarist Schuldiner adopting vocal duties, the band made a major impact on the scene.

随着死亡的吉他手Schuldiner接受主唱的职务，乐队在现实中树立了重要的影响。

But he could still end up breakfasting on Swiss-government issue muesli because all six are accused of nicking around 45 million pounds they should have paid to FIFA.

不过他最后仍有可能沦为瑞士政府&议事餐桌&上的一道早餐，因为这所有六个人都被指控把本应支付给国际足联的大约4500万英镑骗了个精光。