Rapid amplification of genomic ends (RAGE) as a simple method to clone flanking genomic DNA

Publisher： Elsevier

ISSN： 0378-1119

Source： Gene, Vol.194, Iss.2, 1997-07, pp. : 273-276

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

A simple method to design PCR primer to detect genomic DNA of parasites and its application to Dirofilaria immitis

By Nagano I. Zhiliang W. Nakayama M. Takahashi Y.

Molecular and Cellular Probes, Vol. 10, Iss. 6, 1996-12 ,pp. : 423-425

Academic Press

Access to resources Recommend Favorite

Genomic Organization and 5'-Flanking DNA Sequence of the Murine Stomatin Gene (Epb72)

By Gallagher P.G. Turetsky T. Mentzer W.C.

Genomics, Vol. 34, Iss. 3, 1996-05 ,pp. : 410-412

Academic Press

Access to resources Recommend Favorite

Walking into the unknown: a 'step down' PCR-based technique leading to the direct sequence analysis of flanking genomic DNA

By Zhang Z. Gurr S.J.

Gene, Vol. 253, Iss. 2, 2000-08 ,pp. : 145-150

Elsevier

Access to resources Recommend Favorite

Human phosphoribosylformylglycineamide amidotransferase (FGARAT): regional mapping, complete coding sequence, isolation of a functional genomic clone, and DNA sequence analysis

By Patterson D. Bleskan J. Gardiner K. Bowersox J.

Gene, Vol. 239, Iss. 2, 1999-11 ,pp. : 381-391

Elsevier

Access to resources Recommend Favorite

Isolation of genomic sequences flanking a retroviral insertion site using a novel PCR-based method

By Natarajan D. Boulter C.A.

Gene, Vol. 161, Iss. 2, 1995-08 ,pp. : 195-198

Elsevier

Access to resources Recommend Favorite