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03143422001

Roche

Genopure Plasmid Maxi Kit

kit of for 10 isolations from 30 to 150 ml

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About This Item

Code UNSPSC :
41105500
Nomenclature NACRES :
NA.55

Niveau de qualité

Fabricant/nom de marque

Roche

Conditionnement

kit of for 10 isolations from 30 to 150 ml

Description générale

For large-scale (maxi) preparation of plasmid DNA.

Application

The Genopure Plasmid Maxi Kit prepares transfection-grade plasmid DNA in large quantities (up to 500 μg plasmid) from bacterial cultures. Isolated plasmid is suitable for most molecular biology applications:

  • Transfection
  • Southern blotting
  • Sequencing
  • PCR/long PCR
  • Restriction digestion
  • Cloning

Caractéristiques et avantages

The Genopure Plasmid Maxi Kit prepares highly purified plasmid DNA in large quantities using a modified alkaline lysis method.

  • Save time with ready-to-use reagents.
Purify up to 10 samples (10 minutes hands-on-time/75 minutes overall).
  • Purify all sizes and types of plasmid
even BAC DNA, since the crude lysate can be filtered to avoid plasmid shearing.
  • Process multiple samples in parallel
using high speed gravity-flow columns.
  • Eliminate the use of hazardous organic compounds
such as cesium chloride, phenol, chloroform, and ethidium bromide.
  • Obtain higher purity plasmid DNA
over plasmid prepared by 2 x cesium chloride gradient centrifugation.

Composants

  • Suspension Buffer
  • RNase A
  • Lysis Buffer
  • Neutralization Buffer
  • Equilibration Buffer
  • Wash Buffer
  • Elution Buffer
  • NucleoBond AX 500 Columns
  • Folded Filters (240 mm diameter)
  • Sealing Rings

Qualité

Plasmid DNA purified by this kit has been tested for restriction digestion; pUC 19 was isolated from transformed HB101 as described in the protocol. 1 μg of plasmid was completely digested with 1 U Msp I for 2 hours at +37°C, as shown by agarose gel analysis.

Plasmid recovery was tested with 250 μg purified plasmid. The recovery was >90%, with more than 80% in supercoiled form. The yield of plasmid DNA was determined by isolating pBS from DH5a cells. From 150 ml culture volume with a density of A600 between 3 and 6, >400 μg of plasmid DNA was obtained.

The purity (checked by the ratio of A260/A280) is 1.8 + 0.2.

RNA contamination was analyzed with 3 μg pBS purified with the standard procedure and checked by electrophoresis on an agarose gel. No RNA was detected.

The kit components have been tested for the absence of nucleases according to current quality control procedures.

Notes préparatoires

The isolation procedure is based on a modified alkaline lysis protocol and can be divided into the following steps:The bacteria are partially lysed, allowing the plasmid DNA to escape the cell wall into the supernatant. The larger E. coli chromosomal DNA is trapped in the cell wall. The lysate is cleared of cellular debris by filtration or centrifugation, and the plasmid DNA-containing fraction is loaded onto a pre-equilibrated column. Since the cleared lysate is applied to the column in a low-salt buffer, plasmid DNA binds to the macroporous anion-exchange material in the column. Cellular impurities are eluted from the column with a high-salt wash. Finally, the plasmid DNA is eluted from the column. Recovered DNA is precipitated from the eluate to remove salt and concentrate the plasmid.

Remarque sur l'analyse

Sample:
E. coli culture that contains a high-copy number plasmid: 30 to 150 mL bacterial culture
E. coli culture that contains a low-copy number plasmid: 100 to 500 mL bacterial culture
Plasmid Size: The isolation procedure is suitable for all sizes of plasmid. Note: Lysates of larger constructs (up to 100 kb) should be cleared by filtration rather than centrifugation to avoid shearing the plasmid.
Time Required: 75 minutes (including filtration of the lysate)
Typical Yield:
High-copy number plasmid: 3 to 5 μg/mL culture
Low-copy number plasmid: 0.2 to 1 μg/mL culture
Product Purity: Isolated plasmid DNA is free of other bacterial components, including RNA.

Autres remarques

For life science research only. Not for use in diagnostic procedures.

Pictogrammes

FlameCorrosion

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

Eye Dam. 1 - Flam. Liq. 3 - Met. Corr. 1 - Skin Corr. 1

Code de la classe de stockage

3 - Flammable liquids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

100.4 °F

Point d'éclair (°C)

38 °C


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Consulter la Bibliothèque de documents

Sharon Yunger et al.
Nature protocols, 8(2), 393-408 (2013-02-22)
Transcription kinetics of actively transcribing genes in vivo have generally been measured using tandem gene arrays. However, tandem arrays do not reflect the endogenous state of genome organization in which genes appear as single alleles. Here we present a robust
Vivian I Bonano et al.
Nature protocols, 2(9), 2166-2181 (2007-09-15)
Imaging technologies are influencing the way we study regulatory processes in vivo. Several recent reports use fluorescence minigenes to image alternative splicing events in living cells and animals. This type of reporter is being used to generate transgenic mice to
Haruka Sato et al.
eLife, 11 (2022-03-16)
Neuronal abundance and thickness of each cortical layer are specific to each area, but how this fundamental feature arises during development remains poorly understood. While some of area-specific features are controlled by intrinsic cues such as morphogens and transcription factors

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