ConclusionThe concentration and handing time of suspension, slidemaking method and staining time are important factors for an ideal flagellum staining.

細(xì)菌鞭毛染色過程中菌懸液的濃度、菌懸液的處理時間男女高潮无遮挡在线观看动漫、制片方法以及染色時間的長短等條件影響鞭毛染色效果青清草视频。

ConclusionThe concentration and handing time of suspension, slide making method and staining time are important factors for an ideal flagellum staining.

細(xì)菌鞭毛染色過程中菌懸液的濃度、菌懸液的處理時間亚洲免线视频、制片方法以及染色時間的長短等條件影響鞭毛染色效果在线欧美亚洲综合区导航。

Using special stains, one can see that some bacteria have attached to them wavy-looking "hairs" called flagella.Others have only one flagellum.

使用特殊的著色劑后，你會發(fā)現(xiàn)有的細(xì)菌上長著不少波狀的"毛發(fā)"即鞭毛激情第一第二综合天天，而有的細(xì)菌只有一根鞭毛日韩欧美精品原创在线观看。

The flic gene of App was obtained by PCR based on highly homology with Escherichia coli, Salmonella, Shigellosis. Then it was legated to pMD-18T vector. The recombinant plasmid was identified by enzyme and sequence analysis. The 528 bp fragment of flic gene was successfully cloned into pGEX-KG vector, then the recombinant plasmid was transformed into E.

以豬傳染性胸膜肺炎放線桿菌血清Ⅰ型菌株基因組為模板，根據(jù)其鞭毛區(qū)與其它細(xì)菌高度同源性設(shè)計引物杭州最疯狂一级毛片视频，利用PCR方法擴(kuò)增鞭毛蛋白基因flic片段最新自拍网站，將其亞克隆到pMD-18T載體中并進(jìn)行PCR和酶切鑒定国产一区二区三区手机在线观看，再將其亞克隆與載體pGEx-kG分別雙酶切和連接，構(gòu)建重組表達(dá)載體pGEX-flic久.com，并將其轉(zhuǎn)化大腸桿菌工程菌BL21熟女激情视频，進(jìn)行原核表達(dá)。

Objective To detect the expression level of stage-specific genes in Leishmania promastigotes and amastigotes.

摘要目的證明亞馬孫利什曼原蟲前鞭毛體和無鞭毛體的基因表達(dá)水平影音先锋新男人av资源站。

These findings lead to an MSAP/septin-mediated model for flagellar differentiation during spermiogenesis.

免疫螢光定位分析顯示septin7與MSAP共同位於精蟲鞭毛的基底體上中文字幕欧美精品人妻一丘。septin蛋白家族可能參與細(xì)胞質(zhì)分裂及細(xì)胞形態(tài)生成等事件，因此推測MSAP/septin復(fù)合體的功能可能涉及鯉魚精細(xì)胞之極性建立及鞭毛形成欧美无吗不卡高清视频。

The samples were smeared on slides and stained with Giemsas stain. The stained smears were observed microscopically and photographed. It showed that except typical trophozoites in binary fission. the following trophozoites of abnormal morphs were also observed. for instance abnormal trophozoites with binary fission; enlarged trophozoites with round and irregular shaped eosinophilic bodies in the cell plasma; enlarged cells containing round and irregular shaped eosinophilic bodies and flagella; enlarged cells which contain 6 or 8 nuclear-like bodies and flagella, 3 or 4 embryonic forms of daughter trophozoite in one mother trophozoite; 4 trophozoite embryonic forms with fused plasma 3 trophozoites with fused plasma;4 trophozoites with fused plasma; a pair of trophozoite with binary fission fused with another trophozoite;2 pairs of trophozoite with binary fission fused each other; a trophozoite with 1 nuclear only.

結(jié)果 除觀察到典型的營二分裂法繁殖的賈第蟲滋養(yǎng)體外真人黄色网，還可見到多種形態(tài)異常的蟲體，包括99riav.6；蟲體呈非典型二分裂AV免费在线www；滋養(yǎng)體脹大，胞質(zhì)中有團(tuán)塊狀和不規(guī)則形狀的嗜酸性物質(zhì)日韩福利短片在线观看视频免费；在脹大的賈第蟲細(xì)胞內(nèi)含有團(tuán)塊狀和不規(guī)則形狀的嗜酸性物質(zhì)以及鞭毛国产乱伦黄片；在脹大的賈第蟲細(xì)胞內(nèi)含有6或8個核狀物以及鞭毛；在一個母體細(xì)胞中含有3或4個子體細(xì)胞的雛形性淫国产真人高清无码一级黄色网站；胞質(zhì)互相融合的4個滋養(yǎng)體的雛形正在播放国产精品；胞質(zhì)互相觸合的3個滋養(yǎng)體，胞質(zhì)互相融合的4個滋養(yǎng)體日韩毛片视频网站中文字幕；1對營二分裂的滋養(yǎng)體與另一個滋養(yǎng)休互相融合欧美中文字幕日韩综合四季；2對營二分裂的滋養(yǎng)體互相融合；僅有1個細(xì)胞核的滋養(yǎng)體99riav在线。

Methods: We generated amastigotes via in vitro transformation from promastigotes and maintained amastigotes in axenic culture using a modified protocol by increasing the FBS from 20% to 50%.

我們通過改良培養(yǎng)基人人扣B人人干B视频免费播放，將小牛血清從20%提高到50%，在體外將前鞭毛體轉(zhuǎn)化為無鞭毛體高清无码视频免费观看，并在體外純培養(yǎng)。

Objective To explore the protein profile and identify developmentally regulated proteins of the promastigotes and axenic amastigotes with comparative proteomics technique.

摘要目的應(yīng)用蛋白質(zhì)組學(xué)技術(shù)分析杜氏利什曼原蟲前鞭毛體和無鞭毛體蛋白質(zhì)表達(dá)狀況日韩欧美精品视频在线观看_。

Results Approximately 700 protein spots were revealed in equivalent proteins of the promastigotes and axenic amastigotes separated by 2-DE,among which more than 90% protein spots showed equivalent quantity and distribution,with 6 proteins up-regulated and 3 proteins down-regulated in axenic amastigotes compared with promastigotes.

結(jié)果 等量的前鞭毛體與純培養(yǎng)的無鞭毛體總蛋白經(jīng)雙向電泳分離后均可獲近700個蛋白點黄色网址免，其中超過90%的蛋白點的分布和相對強(qiáng)度基本一致。