LCMPROTOCOLS

Slide SectioningParaffin blocks- For DNA analysis:Special LCM processing schedule is followed.The water bath is cleaned using RNAse Zap™, rinsed thoroughly with triple distilled water. The water bath is filled with triple distilled water.All instruments used are cleaned with 100% EtOH (brushes, forceps, pencil).Sections not used are toweled off with kimwipes immediately.A new blade is used for eac......阅读全文

LCM-PROTOCOLS

Slide SectioningParaffin blocks- For DNA analysis:Special LCM processing schedule is followed.The water bath is cleaned using RNAse Zap™, rinsed thoro

Protocols-for-LCM-preparation-and-analysis

Protocols for LCM preparation and analysis I. Preparation, LCM and RNA/DNA extraction of Frozen Tissue SectionsA. EmbeddingB. CuttingC. StainingII. Pr

LCM-实验

试剂、试剂盒 RNaseAway仪器、耗材 胶带LCM 棺子去湿器分液器镊子LCM 系统 Pix Cell Ⅱ无 RNA 酶的管子实验步骤 一、材料1. 缓冲液、溶液和试剂RNaseAway(7000,MolecularBioProducts,SanDiego,CA)2. 特殊设备.胶带LCM 棺子

LCM-实验

            实验方法原理 采用激光切割等技术将生物样品片子等不易观察和检测的样品进行处理的技术,具有简单快捷,效率高等特点。 实验材料 RNaseAway

LCM-实验

LCM实验对(1)切片的病理分析(2)病变程度的分析(3)临床样本收集与参考等都有应用。实验方法原理采用激光切割等技术将生物样品片子等不易观察和检测的样品进行处理的技术,具有简单快捷,效率高等特点。实验材料RNaseAway试剂、试剂盒RNaseAway仪器、耗材胶带LCM 棺子去湿器分液器镊子LC

LCM显微切割

这段时间做的LCM显微切割少量组织,提取ng量级RNA的过程奉上。此类RNA可以经两轮扩增后上样进行基因芯片的研究;或直接作为模板进行RT-PCR的研究。虽然过程复杂一些,目前看效果还是不错。 标本来自新鲜的动物或人体的组织标本,取材后液氮速冻后,-80℃存放备用。 标本冰冻切片的要求:

LCM显微切割

这段时间做的LCM显微切割少量组织,提取ng量级RNA的过程奉上。此类RNA可以经两轮扩增后上样进行基因芯片的研究;或直接作为模板进行RT-PCR的研究。虽然过程复杂一些,目前看效果还是不错。 标本来自新鲜的动物或人体的组织标本,取材后液氮速冻后,-80℃存放备用。 标本冰冻切片的要求: 1.每例标

Laser-Capture-Microdissection-(LCM)

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

Neutralizing-Bioassay-Protocols

Neutralizing Bioassay ProtocolsIntroductionAntibodies that block binding of cytokines to their specific receptors and neutralize their effects are cri

Streptomyces:Protocols/Conjugation

Intergeneric Conjugation and OverlayDescription Transfer of plasmid/cosmid DNA from a host strain, e.g. E.coli ET12567 [pUZ8002], to the recipient str

General-Cloning-Protocols

Large Scale Preps: (See Large scale plsasmid prep protocol for more details)Cultures: Inoculate a 5 mL LB/Amp (50 - 100 µg/mL) culture in early a.m. w

CGH-Protocols-(四)

CGH Image acquisitionImages were acquired through a Zeiss Axiophot fluorescence microscope using a Plan NEOFLUAR oil objective x63, N.A. 1.25 (Zeiss,

Streptomyces:Protocols/PCR

Description Polymerase Chain Reaction (PCR) is a method of amplifying a specific DNA target sequence. The cycle involves denaturing the template doubl

Smolke:Protocols/Western

OverviewBlotting for large V5-tagged proteins in S. cerevisiaeMaterialsY-PER (Pierce)Halt EDTA-free Protease Inhibitor (Pierce)NuPAGE Novex Bis-Tris 4

CGH-Protocols-(一)

Metaphase chromosome preparationMaterials: RPMI 1640 medium fetal calf serum (FCS), 20% Colcemid (e.g. Boehringer Mannheim cell biology reagents, Best

Western-Blotting-Protocols

back to topProtocolStandard vs. Rapid Immunodetection ProceduresThere are two types of protocols for immunodetection: Standard and rapid.Standard vs.

CGH-Protocols-(三)

Hybridizationreagents: labeled tumor and normal-DNA (see protocol Nick translation) salmon sperm DNA, 10 mg/ml (e.g. Promega) human Cot1 DNA, 1 mg/ml

DAPI-Counterstaining-Protocols

实验概要The  blue-fluorescent DAPI nucleic acid stain preferentially stains dsDNA;  it appears to associate with AT clusters in the minor groove. Binding

CGH-Protocols-(二)

DNA preparation by cryotom tissue dissectionPreparations/Materials: Cool cryostat down to -20 to -30°C about 3 hours prior to dissection Label eppendo

Rat-Blood-Collection-Protocols

实验概要The procedure presented below describes a method for collecting rat blood.实验步骤Rat should be fully anesthetized (e.g., unresponsive to toe pinch).1

ORNL-MICROARRAY-HYBRIDIZATION-PROTOCOLS

Direct labeling of total RNA with Cy3 and Cy5:A. MATERIALSRNeasy® Mini Kit (Qiagen; Cat # 74106) SuperScript II RT (200U/µL) (Life Technologies; Cat #

Streptomyces:Protocols/Transformation-by-Electroporation

Description Transform E.coli cells with plasmid/cosmid DNA using the method of electrophoration (inserting plasmids into E.coli).Approx. Duration:Prep

Streptomyces:Protocols/Spore-Prep

Spore Prep - Inoculating & HarvestingDescription A spore prep is a method of preserving a sporulating strain of Streptomyces. The stock is stored in 2

DataONE:Protocols/Find-GEO-reuses

Identify reuses of GEO datasetsAimThe aim of this protocol is to collect data on the reuses of datasets in the published literature. This particular p

Red-Blood-Cell-Lysis-Protocols

实验概要BioLegend’s  Red Blood Cell (RBC) Lysis Buffer (Cat. No. 420301) has been designed,  formulated, and tested to ensure optimal lysis of RBCs in sin

FISH-protocols-for-Drosophila2

 3. Methods3.1 RNA Probe Preparation1.   Different strategies can be used to prepare template DNA for synthesizing antisense RNA probes by in vitro tr

FISH-protocols-for-Drosophila1

.1 RNA Probe Preparation (see Note 1)1.   1.5 mL microcentrifuge tubes or standard 96-well V-bottom microplates.2.   RNAse free water.3.   T7, T3 or S

用于-LCM-的片子的-HE-染色实验

试剂、试剂盒 乙醇曙红Y 梅耶苏木精超纯水二甲苯仪器、耗材 圆锥管镊子破璃染缸实验步骤 一、材料1.缓冲液、溶液和试剂100%乙醇70%乙醇曙红Y(Sigma)梅耶苏木精(Sigma)DEPC处理的超纯水(BiotecxLaboratories,储存于4°C)二甲苯(Sigma)2.特殊设备圆锥管,

用于-LCM-的片子的-HE-染色实验

在进行 LCM 之前,切好的组织样品要固定、染色,必需的话还要脱水。对内脏和淋巴结组织作者采用经典的 HE 染色。一旦片子准备好,LCM 应当在 45 min 内进行。所有的试剂、试管以及其他的用于 RNA 提取的材料应当在染色前准备就绪。本实验来源于 PCR 实验指南(第二版),作者:种康,瞿礼嘉

用于-LCM-的片子的-HE-染色实验

            试剂、试剂盒 乙醇 曙红Y 梅耶苏木精 超纯水 二甲苯 仪器、耗材