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  • Immunofluorescence/ConfocalMicroscopyProtocol

    實驗概要Immunofluorescence is a technique used for light microscopy with a fluorescence microscope and is used primarily on biological samples. This technique uses the specificity of antibodies to their antigen to target fluorescent dyes to specific biomolecule targets within a cell, and therefore allows visualization of the distribution of the target molecule through the sample. Immun......閱讀全文

    Use-of-Transmission-Electron-Microscopy

    ?Use of Transmission Electron MicroscopyOverviewA protocol describing the use of Zeiss EM9-S transmission electron microscopy is presented.?MaterialZe

    Generic-Fixation-for-Electron-Microscopy

    Generic Fixation for Electron MicroscopyThe best way to fix a sample for electron microscopy is to follow a procedure developed and proven by others.

    Immunofluorecence-P...

    實驗概要Immunofluorescence ?is a technique used for light microscopy with a fluorescence microscope ?and is used primarily on biological samples. This tec

    細胞組分和細胞器——細胞骨架

    Fixation and Immunofluorescence of the Cytoskeleton?(Mitchison Lab)??Recycling Tubulin?(Mitchison Lab)??Labeling Tubulin and Quantifying Labeling Stoi

    Basic-Method-for-Indirect-Immunofluorescence-Labeling

    Basic Method for?Indirect?Immunofluorescence LabelingBackgroundThis is the method for?indirect?immunofluorescence labeling; that is, the antibodies?do

    Fixation-and-Embedding-of-Microtubules-for-Electron-Microscopy

    (This procedure can also be used for virtually any material that must be pelleted prior to fixation and thin sectioning)Primary fix:2% glutaraldehyde

    Specimen-Preparation-for-Scanning-Electron-Microscopy

    Specimen Preparation for Scanning Electron MicroscopyWe recommend consultation with one of the lab directors before preparing specimens. The methods p

    Chlamydomonas-Fixation-for-Transmission-Electron-Microscopy

    Chlamydomonas?Fixation for Transmission Electron MicroscopySolutions:Chlamydomonas?culture medium + 2% glutaraldehyde (5 ml medium + 0.9 ml 25% glutar

    Tetrahymena-Fixation-for-Transmission-Electron-Microscopy

    Tetrahymena?Fixation for Transmission Electron MicroscopyPellet Tetrahymena cells in a clinical centrifuge.OPTIONAL: Suspend cells in HNMK (50 mM HEPE

    Silver:-TimeLapse-Microscopy

    Pad Preparation1. Microwave 2% agarose (mix of low-melt and normal, to taste) in Thorn media (see below). (If you have used different percentages of a

    Negative-Stain-Electron-Microscopy-of-Microtubules

    Negative staining is a rapid, qualitative method for analyzing microtubule structure at the EM level. Because negative staining involves deposition of

    FV1200-Confocal/FLIM/FCS共享應用

    儀器名稱:FV1200 Confocal/FLIM/FCS儀器編號:17003902產地:日本生產廠家:Olymplus型號:FV1200出廠日期:201504購置日期:201703所屬單位:生命學院>蛋白質研究技術中心>細胞影像平臺>設施細胞影像平臺放置地點:生物醫學館U6-113固定電話:010

    Olymplus-FV1200-Confocal/FLIM/FCS共享

    儀器名稱:FV1200 Confocal/FLIM/FCS儀器編號:17003902產地:日本生產廠家:Olymplus型號:FV1200出廠日期:201504購置日期:201703樣品要求:免疫熒光樣品盡可能背景少一些;組織切片盡量不要切的太厚,染色完成后盡量多洗幾遍以減少背景光的干擾;樣品做完之

    Intracellular-Cytokine-Staining-Protocol

    實驗概要A ?modification of the basic immunofluorescence staining and flow ?cytometric analysis protocol can be used for the simultaneous analysis ?of surf

    用離子流技術和熒光蛋白提高胞內外Ca2+和H+的時空分辨率

    關鍵詞:花粉管(Pollen tube),鈣信號(Calcium signaling),質子信號(Proton signaling),細胞分化(Cell polarization)參考文獻:Erwan Michard. et al. Sexual Plant Reproduction, 2008,

    Preparation-Of-Ciliated-Protozoa-For-Scanning-Electron-Microscopy

    Preparation Of Ciliated Protozoa For Scanning Electron MicroscopyGeneral notes: The same procedures are used to fix and stain cells for SEM and for TE

    免疫電鏡(Immune-electron-microscopy)原理

    (一)? 原理免疫電鏡技術是免疫化學技術與電鏡技術結合的產物,是在超微結構水平研究和觀察抗原、抗體結合定位的一種方法學。它主要分為兩大類:一類是免疫凝集電鏡技術,即采用抗原抗體凝集反應后,再經負染色直接在電鏡下觀察;另一類則是免疫電鏡定位技術。該項技術是利用帶有特殊標記的抗體與相應抗原相結合,在電子

    免疫電鏡(Immune-electron-microscopy)原理

    (一)??原理?免疫電鏡技術是免疫化學技術與電鏡技術結合的產物,是在超微結構水平研究和觀察抗原、抗體結合定位的一種方法學。它主要分為兩大類:一類是免疫凝集電鏡技術,即采用抗原抗體凝集反應后,再經負染色直接在電鏡下觀察;另一類則是免疫電鏡定位技術。該項技術是利用帶有特殊標記的抗體與相應抗原相結合,在電

    EPON-resin-mixture-for-transmission-electron-microscopy

    EPON resin mixture for transmission electron microscopyFor Epon WPE 153:~120 ml~60 ml~30 mlMix A:Embed 81244 ml22.1 ml11.1 mlDDSA67 ml33.3 ml16.7 mlMi

    信號傳導

    Cytokine Bioassays?(eBioscience)Biological activity of cytokines and their concentrations are commonly measured by cellular proliferation of primary c

    信號傳導

    Cytokine Bioassays?(eBioscience)Biological activity of cytokines and their concentrations are commonly measured by cellular proliferation of primary c

    PCR-protocol

    PCR reactionProtocol for 50μl reaction - adjust amounts if necessary, for a 20μl reaction use the same volumes of primer and dNTP-mix, but adjust the

    ELISPOT-protocol

    實驗概要The procedure ?below is a general guideline procedure for ELISPOT. Abcam ELISPOT kits ?have been designed for detection of various cytokines and g

    NAi-protocol

    siRNA protocolsOur current strategy with siRNA is to synthesis relatively small amounts enzymatically and use these to test for efficiency by western

    Immunoblot-Protocol

    This method was successful in our lab using prostate tissue and for our specific objectives. Investigators must be aware that they will need to tailor

    ELISPOT-Protocol

    實驗概要The ?Elispot (Enzyme Linked Immuno-Spot) assay provides an effective method ?of measuring the antibody or cytokine production of immune cells on t

    Immunoprecipitation-Protocol

    實驗概要Immunoprecipitation ?is a procedure by which proteins or peptides that react specifically ?with an antibody are removed from solution and examined

    ELISA-protocol

    ELISA protocol:1.取5-10ul BMMY表達上清用0.05M NaHCO3稀釋到100ul鋪ELISA板,37度或室溫振蕩大于1小時。注意一定要做一個GS115空菌株表達上清作為陰性對照,最好還找一個帶有histag的蛋白作為陽性對照。2.TPBS洗板3次,方法:倒掉鋪板液,倒置于

    RNAi-protocol

    ?siRNA protocolsOur current strategy with siRNA is to synthesis relatively small amounts enzymatically and use these to test for efficiency by western

    RLGS-protocol

    A. Preparation of DNA SolutionIn the case of rice, for example    This method may be appllicable for many grass species and some other plants.????????

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