E.Z.N.A.TMYeastRNAKitSpinProtocol
实验概要The E.Z.N.A.® Yeast RNA Kit allows convenient isolation of high-quality total RNA from a wide variety of yeast species. Up to 2 x 107 log-phase cultured yeast cells can be processed. The system combines the reversible nucleic acid-binding properties of HiBind® matrix with the speed and versatility of spin column technology to yield approximately 30 ug of RNA, with an A260/A280 ratio of 1.7-1.9. Purified RNA......阅读全文
E.Z.N.A.TM－Yeast－RNA－Kit－Spin－Protocol
实验概要The E.Z.N.A.® Yeast RNA Kit allows convenient isolation of high-quality total RNA from a wide variety of yeast species. Up to 2 x 107 log-phase cu
Fastfilter－Plasmid－Midi－Kit－Spin－Protocol
实验概要The E.Z.N.A.TM Fastfilter Plasmid Midi Kit combines the power of HiBind® technology with the time-tested consistency of alkaline-SDS lysis of
Fastfilter－Plasmid－Midi－Kit－Vacuum/Spin－Protocol
实验概要The E.Z.N.A.TM Fastfilter Plasmid Midi Kit combines the power of HiBind® technology with the time-tested consistency of alkaline-SDS lysis of
E.Z.N.A.®－Plasmid－Maxi－Kit－Spin－Protocol
实验概要This Protocol is designed to isolate 500-1200 ug of high Copy-Number plasmids or 50-400 ug of low Copy-Number Plasmids from 200 ml overnight c
Vacuum/Spin－Protocol－for－Tissue－DNA－Extraction
实验概要The E.Z.N.A.® Tissue DNA Kit provides a rapid and easy method for the isolation of genomic DNA for consistent PCR and Southern analysis. Up to 3
Genomic－DNA－Extraction－－PureLink™
实验概要The PureLink™ Genomic DNA Purification Kit allows rapid and efficient purification of genomic DNA. The kit is designed to efficiently isolate g
E.Z.N.A.®－Total－RNA－Midi－Kit－Protocol－DNase－I－digestion－Protocol
实验概要E.Z.N.A.® Total RNA Midiprep Kit provides a rapid and easy method for the isolation of up to 600 ug of total RNA from cultured eukaryotic cells,
E.Z.N.A.®－Total－RNA－Maxi－Kit－Protocol－for－Animal－Tissues
实验概要The E.Z.N.A.® Total RNA Maxi Kit uses HiBind® matrix spin-column technology to isolate up to 5 mg total cellular RNA from a variety of sources
E.Z.N.A.®－Total－RNA－Midi－Kit－Protocol－for－Eukaryotic－Cells－and－Tissues
实验概要E.Z.N.A.® Total RNA Midiprep Kit provides a rapid and easy method for the isolation of up to 600 ug of total RNA from cultured eukaryotic cells,
Vacuum/Spin－Protocol－for－Isolating－DNA－from－Blood－with－Nucleated－Red
实验概要DNA isolation from fish or avian blood sample can be difficult because it contains nucleated red blood cells. E.Z.N.A. NRBC Blood DNA Kit is de
Fungal－Midi－DNA－Kit－Optional－protocol
实验概要This protocol is designed for isolation of genomic DNA from fresh, frozen, or dried specimens from fungal samples contains higher phenolic mat
EZ－96®－M13－Isolation－Spin－Protocol
实验概要The E.Z.N.A.™ family of products is an innovative system that radically simplifies the extraction and purification of nucleic acids from a vari
Acid－Phenol－Yeast－RNA－Prep
This is the preferred method for yeast RNA preparationuse Gloves and RNAse free solutions throughout.1. Use a YPD overnight culture to innoculate fres
RNA－Isolation－Protocol
Stabilize RNAStart with 15 ml E. coli Culture containing 7.5* 109 cells (OD600= 0.2 Dilute cells or scale up)Pipet 30 ml of RNAProtect Bacteria Reagen
RNA－Isolation－Protocol
RNA Isolation Protocol(Revised 5-15-2003)Stabilize RNAStart with 15 ml E. coli Culture containing 7.5* 109 cells (OD600= 0.2 Dilute cells or scale up)
Miniprep/Kitfree－highthroughput－protocol
BackgroundThis protocol is adapted from "Molecular Cloning: A Laboratory Manual", Second Edition, Sambrook, Fritsch, and Maniatis. It is a quick, inex
Fungal－Midi－DNA－Kit－Protocol－for－Fresh/Frozen－Specimens
实验概要This protocol is suitable for most fresh or frozen tissue samples allowing more efficient recovery of DNA. However, due to the tremendous variat
Arabidopsis－RNA－extraction－protocol
1-2 g fresh material, freezer-dried, ground with 0.2g sand (if necessary), and then homogenized with 10ml RNA extraction buffer (see below). Spin
Arabidopsis－RNA－extraction－protocol
1-2 g fresh material, freezer-dried, ground with 0.2g sand (if necessary), and then homogenized with 10ml RNA extraction buffer (see below).Spin at 8,
E.Z.N.Z.TM－MicroElute－RNA－Cleanup－Protocol
实验概要This protocol is designed to recovery RNA from enzymatic reactions such as DNase I digestion, In vitro transcription, etc. For RNA desalting o
微量RNA的抽提RNeasy－MinElute－Spin－Column
·为了更好地裂解，细胞数不能大于5×105，细胞过多会减低产率和纯度。 准备工作： 1.在 24 ml 96－100％乙醇 中加入 6 ml 去RNA酶的水。 2.在每 1 ml Buffer RLT 中加入10 ml β-ME (加入β-ME的Buffer RLT可在室温下放置1
E.Z.N.A.®－Plasmid－Maxi－Kit－vacuum－Protocol
实验概要This Protocol is designed to isolate 500-1200 ug of high Copy-Number plasmids or 50-400 ug of low Copy-Number Plasmids from 200 ml overnight c
Northern－protocol(RULES－FOR－RNA－WORK)
1. Wear gloves at all time including filling pipet tip in racks, filling jars with Eppendorf tubes, and weighing chemicals to prepare solution
RNA－Isolation－From－Animal－tissue－or－cell－culture
实验概要This method is designed for most animal tissues and culture cells. For RNA isolation from fibrous tissue, follow the specialized protocol on pag
E.Z.N.Z.TM－MicroElute－RNA－Desalting－and－Concentration－protocol
实验概要This protocol is designed to clean up and concentrate RNA from various sources such as RNA isolated with RNA-solv® Reagent and other phenol involv
Chemicon公司的CpGenome－DNA－Modification－Kit－的protocol修正
我用了快4个月这个试剂盒了，下面是一些总结出来的经验，我现在诱变每次都很成功了，呵呵：）1. 我溶NaOH的水PH值大概在6.5左右，所以我每次调Reagent I的时候3MNaO0H基本都要加150uL左右。2. 解链时用50度水浴15分钟。3. 加入Reagent I后，50度水浴16小时。4.
E.Z.N.A.®－Protocol－for－Bacteria
实验概要The E.Z.N.A. Total RNA Kit can be modified for isolation of RNA from bacterial cultures. Only cells growing at log phase should be used. Measu
Adiponectin－Replenishment－Ameliorates－ObesityRelated－Hypertension（二）
Methods Animal and Animal Treatment KKAy male mice were purchased from Japan CLEA (Tokyo, Japan). This strain is a cross between black KK fema
The－ribonuclease－protection－assay－(RPA)
The ribonuclease protection assay (RPA) is a highly sensitive and specific method for the detection of mRNA species. The assay was made possible by th
SYBR－Green－Quantitative－PCR－Protocol
SummaryQuantitative PCR is a method used to detect relative or absolute gene expression level. All qPCR involves the use of fluorescence to detect the