U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Method of producing a DNA library using positional amplification based on the use of adaptors and nick translation

Patent 6828098 Issued on December 7, 2004. Estimated Expiration Date: Icon_subject May 18, 2021. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

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Inventors

Assignee

Application

No. 09860738 filed on 05/18/2001

US Classes:

435/6, Involving nucleic acid435/91.1, Polynucleotide (e.g., nucleic acid, oligonucleotide, etc.)435/91.2Acellular exponential or geometric amplification (e.g., PCR, etc.)

Examiners

Primary: Horlick, Kenneth R.

Attorney, Agent or Firm

Foreign Patent References

  • 0684 315 EP 03/01/1995
  • WO 9324654 WO 12/01/1993
  • WO 9815652 WO 04/01/1998
  • 9918241 WO 04/01/1999
  • 0018960 WO 04/01/2000
  • 0024929 WO 05/01/2000
  • 0028084 WO 05/01/2000
  • 0060121 WO 10/01/2000

International Classes

C12Q 168
C12P 1934

Abstract

The disclosed invention relates to general and specific methods to use the Primer Extension/Nick Translation (PENT) reaction to create an amplifiable DNA strand, called a PENTAmer. A PENTAmers can be made for the purpose of amplifying a controlled length of DNA located at a controlled position within a DNA molecule, a process referred to as Positional Amplification by Nick Translation (PANT). In contrast to PCR, which amplifies DNA between two specific sequences, PANT can amplify DNA between two specific positions. PENTAmers can be created to amplify very large regions of DNA (up to 500,000 bp) as random mixtures (unordered positional libraries), or as molecules sorted according to position (ordered positional libraries). PANT is fast and economical, because PENTAmer preparation can be multiplexed. A single PENTAmer preparation can include very complex mixtures of DNA such as hundreds of large-insert clones, complete genomes, or cDNA libraries. Subsequent PCR amplification of the preparation using a single specific primer can positionally amplify contiguous regions along a specific clone, along a specific genomic region, or along a specific expressed sequence.

Other References

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