GeneralCloningProtocols

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. with a single colony. Use all 5 mL to inoculate a 500 mL LB/Amp culture in the evening. Alternatively the 5 mL culture can also be set up as an overnight culture.Save 1 mL for a glycerol stock if necessary (see step 6c, below). Prepare remainder according to ......阅读全文

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

Human-Embryonic-Stem-(ES)-Cell-Protocols——General-notes-on-ES-cell-culture

hES media has a two week shelf life.hES cells should be cultured in 4, 6, 24, 48, 96 well plates. Growing cells in flasks is not recommended because i

Targeted-Gene-Replacement-in-Fungal-Pathogens-via-Agrobacterium-...

Genome sequence data on fungal pathogens provide the opportunity to carry out a reverse genetics approach to uncover gene function. Efficient meth

Bacterial-transformation

IntroductionTransformation is the process of introducing foreign DNA (e.g plasmids, BAC) into a bacterium. Bacterial cells into which foreign DNA can

General-Reference

Units1 mg = 10-3 g1 ug = 10-6 g1 ng = 10-9 g1 pg = 10-12 g1 kb of double stranded DNA = 660 kD 1 kb of single stranded DNA = 330 kD 1 kb of single str

Fusion-and-Cloning

Author: Nanci DonackiSource: Contributed by Nanci DonackiAbstract: Procedure for establishing hybridoma in one stepReagents(StemCell Technologies, Inc

Fusion-and-Cloning

ReagentsMedium A - Pre-fusion Medium and Hybridoma Expansion MediumMedium B - Fusion Medium Medium C - Hybridoma Recovery MediumMedium D - Hybridoma S

DNA克隆

DNA克隆(主要内容如下)·         General Procedure·         PCR Cloning·         Subcloning·         ET Cloning·         Vector Preparation·         Ligation Re

LCM-PROTOCOLS

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

immunofluorescence-of-general-cell-by-Peprotech

实验概要The following protocol provides a method of immunofluorescence of general cell by Peprotech.实验步骤Please refer to the antibody Product Information S

immunofluorescence-of-general-PBMC-by-Peprotech

实验概要The following protocol provides a method of immunofluorescence of general PBMC by Peprotech.实验步骤The following protocol used human PBMC that were

ELISA-Protocol-(General-Guidelines)

实验概要Sandwich  enzyme-linked immunosorbent assays (ELISAs) involve attachment of a  capture antibody to a solid phase support. Samples containing known

ELISA-Protocol-(General-Guidelines)

实验概要Sandwich  enzyme-linked immunosorbent assays (ELISAs) involve attachment of a  capture antibody to a solid phase support. Samples containing known

DNA-EXTRACTION-PROCEDURE--GENERAL

Grow cells overnight in 500 ml broth medium.Pellet cells by centrifugation, and resuspend in 5 ml 50 mM Tris (pH 8.0), 50 mM EDTA.Freeze cell suspensi

General-Laboratory-Methods-for-Tetrapyrroles

There are thousands of porphyrins and metalloporphyrins, and hundreds of new derivatives appear each year. This variety arises because the cyclic

基因cloning经验指南

我们克隆基因的时候,往往可以通过一些途径(如pcr,EST库或者文库筛选)得到基因的部分片段。然后通过3'race 和 5'race 方法往两端延伸。有时会出现无法延伸的状况,如果你超作没有失误的话,这时候很有可能是你模板GC含量过高的缘故,普通pcr 是没有办法延伸的,可以用扩高g

Genomic-Cloning-Technical-Manual

Genomic Cloning Technical ManualAn optimal strategy for genomic cloning should meet three requirements: 1) a maximum number of recombinants should be

Cloning-by-Limiting-Dilution-of-Hybridoma

Author: Nanci DonackiSource: Contributed by Nanci DonackiDate Added: Tue May 14 2002Date Modified: Tue Apr 27 2004MaterialsDMEM, high glucose (Life Te

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

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-(一)

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

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

Neutralizing-Bioassay-Protocols

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

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,

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

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-(二)

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

“电子”基因克隆-(sillcon-cloning)

利用计算机来协助克隆 基因,称为“电子”基因克隆 (sillcon cloning),是与定位克隆 、定位候选克隆 策略并列的方法之一,即采用生物信息学的方法延伸EST序列,以获得基因部分乃至全长的cDNA序列。EST数据库的迅速扩张,已经并将继续导致识别与克隆 新基因策略发生革命性变化。1

Cloning-PCR-products-using-TA-vectors

Cloning PCR products using TA vectorsby Paul N. Hengen, Ph.D. *Methods and reagents is a unique monthly column that highlights current discussions in