1992
DOI: 10.1007/bf00028908
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New plant binary vectors with selectable markers located proximal to the left T-DNA border

Abstract: Five new binary vectors have been constructed which have the following features: (1) different plant selectable markers including neomycin phosphotransferase (nptII), hygromycin phosphotransferase (hpt), dihydrofolate reductase (dhfr), phosphinothricin acetyl transferase (bar), and bleomycin resistance (ble); (2) selectable markers are located near the T-DNA left border and; (3) selectable marker and beta-glucuronidase (uidA) reporter genes are divergently organized for efficient expression, and can easily be … Show more

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Cited by 565 publications
(406 citation statements)
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“…The lengths of the amplified sequences were 1867 bp (AtCKX1), 1603 bp (AtCKX2), 1452 bp (AtCKX3), 1926 bp (AtCKX4), 1817 bp (AtCKX5), and 1828 bp (AtCKX6). All promoter sequences were inserted into vector pGPTV-BAR (Becker et al, 1992) upstream of the GUS reading frame. Dideoxy sequencing of the amplified DNA fragments was performed with an ABI PRISM BigDye Terminator cycle sequencing reaction kit (Perkin-Elmer Applied Biosystems Division) to exclude PCR and cloning errors.…”
Section: Generation Of Atckx-overexpressing Plants and Transgenic Plamentioning
confidence: 99%
“…The lengths of the amplified sequences were 1867 bp (AtCKX1), 1603 bp (AtCKX2), 1452 bp (AtCKX3), 1926 bp (AtCKX4), 1817 bp (AtCKX5), and 1828 bp (AtCKX6). All promoter sequences were inserted into vector pGPTV-BAR (Becker et al, 1992) upstream of the GUS reading frame. Dideoxy sequencing of the amplified DNA fragments was performed with an ABI PRISM BigDye Terminator cycle sequencing reaction kit (Perkin-Elmer Applied Biosystems Division) to exclude PCR and cloning errors.…”
Section: Generation Of Atckx-overexpressing Plants and Transgenic Plamentioning
confidence: 99%
“…The pGPTVkan-LBC3, kindly provided by Mette Groenlund (University of Aahrus, Denmark), is a derivative of the pGPTVkan plasmid (Becker et al 1992), containing the 1.9 kb fragment of the Glycine max LBC3 promoter cloned into SalI-BamHI sites.…”
Section: T-dna Constructs Preparationmentioning
confidence: 99%
“…Two series of binary vectors, pB and pH types, carrying a phosphinothricin N-acetyltransferase (BAR) or a hygromycin phosphotransferase gene (HPT), respectively, were similarly constructed from pGPTV-BAR or pGPTV-HYG (Becker et al, 1992) as follows.…”
Section: Construction Of Binary Vectors and Transformation Of Plantsmentioning
confidence: 99%