SilaneandPolyLLysineCoatingofMicroscopeSlides

1) Wash slides in Decon solution for 30 minutes.2) Wash slides in running tap water for 30 minutes.3) Wash slides in distilled water for 2 x 5 minutes.4) Wash slides in 95% ethanol for 2 x 5 minutes.5) Air dry in a dust free environment for 5 minutes.Poly-L-Lysine Coatinga) Smear 20ul of poly-l-lysine over each slide. b) Air dry in a dust free environment.Silated Slidesa) To 300mls acetone add 6mls Aminopropyltr......阅读全文

Silane-and-PolyLLysine-Coating-of-Microscope-Slides

1) Wash slides in Decon solution for 30 minutes.2) Wash slides in running tap water for 30 minutes.3) Wash slides in distilled water for 2 x 5 minutes

Live-imaging-with-Drosophila-tissue-culture-cells2

Materials & ReagentsDrosophila Schneider S2 cellsSchneiders Medium (GIBCO/Invitrogen), 10% fetal calf serum, Antibiotics (Sigma A5955)Depression slide

Use-of-SemiThin-Cryosections-for-Light-Microscopy.

Use of Semi-Thin Cryosections for Light Microscopy.Semi-thin sections can be obtained from frozen blocks of cryoprotected biological material by secti

Microwave-citrate-Pretreatment-of-Paraffin-Sections

1.Deparaffinize slides a (after drying thoroughly overnight at RT) in 2 changes of xylene (or xylene substitute) for 10 mins each.2.Transfer slides to

Immunofluorescence-/-Confocal-Microscopy-Protocol

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

Immunofluorescence-/-Confocal-Microscopy-Protocol

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

Protocol-to-Count-Cell-Number-of-Preimplantation-Embryos

Protocol to Count Cell Number of Preimplantation Embryos using Nuclear Staining with Hoechst 33342 or DAPI  Introduction The following is a simple pro

3HThymidine-Uptake-by-Cultured-Cells

Materials Fibroblast cells in log phase growthCa , Mg free-phosphate buffered saline (PBSA)5% (w/v) Glutaraldehyde (GTA)2% (w/v) Perchloric Acid (PCA)

HThymidine-Uptake-by-Cultured-Cells

H-Thymidine Uptake by Cultured CellsLEVEL IIMaterialsFibroblast cells in log phase growthCa, Mg free-phosphate buffered saline (PBSA)5% (w/v) Glutaral

MetalEnhanced-Immu...-(二)

实验步骤1. Preparation of Fluorescein-Doped PVA FilmsThe 0.5% PVA solution containing disodiumfluorescein was spin-coated  on slide substrates at 3,000 rp

3HThymidine-Uptake-by-Cultured-Cells

3H-Thymidine Uptake by Cultured Cells  OverviewA radioactive method for measuring cultured cell growth with 3H-thymidine is described here. MaterialFi

Coating-of-Platelets-with-Antibody-in-vitro

OUTLINEAntibody-coated platelets (opsnized) may be used in the subsequent thrombophagocytosis assay. PROTOCOLResuspend 1.6x10^8 of CMFDA-labeled plate

Live-imaging-with-Drosophila-tissue-culture-cells1

IntroductionLive imaging provides an important complementation to the "snapshot" view obtained in fixed tissue by immunofluorescence. It allows follow

TUNEL-PROCEDURE-IN-BOVINE-EMBRYOS

Materials8% (w/v) paraformaldehyde stock solution:  Dissolve 8 g of powdered paraformaldehyde in 100 ml water. Heat and stir (55-60 C – do not go high

TUNEL-PROCEDURE-IN-BOVINE-EMBRYOS

Materials8% (w/v) paraformaldehyde stock solution:  Dissolve 8 g of powdered paraformaldehyde in 100 ml water. Heat and stir (55-60 C – do not go high

Tunel-Procedure-in-Bovine-Embryos-牛胚胎TUNEL检测凋亡

Materials8% (w/v) paraformaldehyde stock solution: Dissolve 8 g of powdered paraformaldehyde in 100 ml water. Heat and stir (55-60 C – do not go highe

MetalEnhanced-Immu...-(一)

实验概要The surface-confined assay format is one of the most convenient detection formats used in many immunoassays. Fluorescence emission from monola

Measurement-with-the-Light-Microscope

Measurement with the Light MicroscopeYour microscope may be equipped with a scale (called a reticule) that is built into one eyepiece. The reticule ca

USE-OF-THE-LIGHT-MICROSCOPE

USE OF THE LIGHT MICROSCOPEEach time the microscope is to be used it should be set up correctly to give a good image. Most often users forget to adjus

Blocking-cDNA-arrays-printed-on-amine-slides

Department of Crop SciencesCollege of Agricultural, Consumer, and Environmental SciencesUniversity of Illinois at Urbana-ChampaignPurpose: After spott

Transmission-Electron-Microscope-(TEM)

所谓TEM,就是一个放大镜叠加了一台照相机。这台放大镜的放大倍数比较高,可高达一百万倍。当然,抛开分辨率谈放大倍数都是耍流氓,那么,TEM的分辨率有多高呢?答案是 it depends。一般来说,TEM的分辨率要在1到2个纳米,STEM更高,但是STEM得成像技术类似于SEM,但用的不是二次电子。我

Double-immunofluore...

实验概要We provide a protocol for immunofluoresent double staining incubating the antibodies together.In order to be able to examine the co-distributi

Mapping-Protein-Distributions-on-Polytene-Chromosomes-by-Immunostaining1

INTRODUCTIONThe formidable size and structure of polytene chromosomes allowmapping of chromosomal protein distributions at very high resolution.This p

偏光显微镜(Polarizing-microscope)

一、偏光显微镜的特点偏光显微是鉴定物质细微结构光学性质的一种显微镜。凡具有双折射性的物质,在偏光显微镜下就能分辨的清楚,当然这些物质也可用染色法来进行观察,但有些则不可能,而必须利用偏光显微镜。偏光显微镜的特点,就是将普通光改变为偏振光进行镜检的方法,以鉴别某一物质是单折射性(各向同性)或双折射性(

Standard-Protocols-Autoradiography-(35S)

Remove Kodak NTB2 nuclear emulsion from fridge and place at 42oC for around 30-60 mins (until melted).Make up the developer and the fixer and place in

Autoradiography-(35S)

Remove Kodak NTB2 nuclear emulsion from fridge and place at 42oC for around 30-60 mins (until melted).Make up the developer and the fixer and place in

Immunofluorescence-Microscopy-Protocol

实验概要Immunofluorescence  allows the imaging of a specific factor in cells or tissue sections  through the use of a specific antibody chemically which i

Immunofluorescence-Microscopy-Protocol

实验概要Immunofluorescence  allows the imaging of a specific factor in cells or tissue sections  through the use of a specific antibody chemically which i

Setup-and-use-of-a-twolaser-multiphoton-microscope

Setup and use of a two-laser multiphoton microscope for multichannel intravital fluorescence imagingDavid Entenberg,1 Jeffrey Wyckoff,1 Bojana Gligori

关于多聚赖氨酸的配制、保存、使用总结与问题1

因为自己做PC12细胞培养,想在接种前将培育皿用多聚赖氨酸包被,到论坛里搜索了下,关于多聚赖氨酸的帖子不少,看了一些帖子,将大部分收集在此。个人觉得关于多聚赖氨酸的配置、保存、使用各方面问题,这些帖子里面都解释了。注:我只是摘了一个帖子里某段或某句话。一般一段话来自某一位朋友。一、常用的多聚赖氨酸包