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69281 DNase Shotgun® Cleavage Kit

69281
  
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Áttekintés

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Description
Overview

This product has been discontinued.





The DNase Shotgun® Cleavage Kit is designed to generate random DNA fragments from any DNA sample in preparation for cloning. The sample DNA is cleared with DNase I in the presence of Mn2+, which causes random double-stranded cleavage of the DNA molecule (Anderson 1981). The DNase I in the kit is specially prepared in a buffer lacking Mg2+ to prevent single-strand nicking.

Fragments of almost any size can be generated by adjusting the amount of enzyme and/or time of reaction. Specific size ranges can be isolated by agarose gel electrophoresis, and the ends repaired using a DNA polymerase (e.g., to generate blunt ends treat with T4 DNA polymerase in the presence of dNTPs). The Single dA Trailing Kit repairs DNA ends and adds a 3′-dA residue. The processed DNA fragments can be easily cloned into any vector with single 3′-dT or 3′-dU overhangs, such as one of the Novagen AccepTor™ Vectors. Advantages of this cloning strategy include: prevention of tandem inserts, low nonrecombinant background, and no requirements for special linkers or additional fractionation steps. This patented approach is used to generate protein domain expression libraries with the Novagen NovaTope® System.

Catalogue Number69281
Brand Family Novagen®
References
ReferencesAnderson, S. 1981. Nucleic Acids Res. 9, 3015.
Product Information
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Biological Information
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Ship Code Shipped with Blue Ice or with Dry Ice
Toxicity Multiple Toxicity Values, refer to MSDS
Storage -20°C
Avoid freeze/thaw Avoid freeze/thaw
Do not freeze Ok to freeze
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Global Trade Item Number
Katalógusszám GTIN
69281 0

Documentation

DNase Shotgun® Cleavage Kit Certificates of Analysis

TitleLot Number
69281

References

Hivatkozások áttekintése
Anderson, S. 1981. Nucleic Acids Res. 9, 3015.

Citations

Titulus
  • G. Gupta, et al. (1999) Simplified gene-fragment phage display system for epitope mapping. Bio/Techniques 27, 328-334.
  • C. Hatfield, et al. (1997) Epitope mapping by recombination PCR mutagenesis. Bio/Techniques 22, 332-337.