<p>PCR products amplified from the progenies of KS2-27, KS2-45, KS2-70, KS2-27-1 and KS2-45-1 genomic DNA using the primers Cas9p-F and Cas9p-R. The numbers above the gel image refer to individual offspring of KS2-27, KS2-45, KS2-70, KS2-27-1 and KS2-45-1, respectively. M: DNA molecular weight marker; Plasmid: pC-ERF922; Wild-type: genomic DNA from Kuiku131.</p
Sequence-tagged sites (STSs) facilitate the conversion of a genetic map into a physical map, provide...
PCR is a powerful tool for the amplification of genetic sequences but sometimes, even though using a...
Early determination of transgenic plants that are homozygous for a single locus T-DNA insert is high...
<p>The weight of DNA marker was shown on the left. <b>A</b> PCR identification of the integration of...
Abstract: A high throughput rice DNA mini-preparation method was developed. The method is suitable f...
Not AvailableThe realization of yield potential of rice (Oryza sativa L.) hybrids developed through ...
A pilot binary vector was constructed to assess the potential of the 2 T-DNA system for generating s...
Bi-allelic mutant lines induced by clustered regularly interspaced short palindromic repeats (CRISPR...
<p>(a) PCR analysis of T<sub><b>1</b></sub> transgenic rice plants for marker excision. (b) RT-PCR a...
Now that sequencing of the rice genome is nearly completed, functional analysis of its large number ...
<p>A) Photographs were taken of six week-old seedlings grown under greenhouse conditions. B) Picture...
The occurrence of genomic modifications in transgenic rice plants recovered from protoplasts and the...
The present study was designed to establish a qualitative detection method based on conventional and...
[[abstract]]With the completion of the rice genome sequencing project, the next major challenge is t...
Hybrid rice, grown in more than 50 % of the area in China, is be-coming popular in other Asian count...
Sequence-tagged sites (STSs) facilitate the conversion of a genetic map into a physical map, provide...
PCR is a powerful tool for the amplification of genetic sequences but sometimes, even though using a...
Early determination of transgenic plants that are homozygous for a single locus T-DNA insert is high...
<p>The weight of DNA marker was shown on the left. <b>A</b> PCR identification of the integration of...
Abstract: A high throughput rice DNA mini-preparation method was developed. The method is suitable f...
Not AvailableThe realization of yield potential of rice (Oryza sativa L.) hybrids developed through ...
A pilot binary vector was constructed to assess the potential of the 2 T-DNA system for generating s...
Bi-allelic mutant lines induced by clustered regularly interspaced short palindromic repeats (CRISPR...
<p>(a) PCR analysis of T<sub><b>1</b></sub> transgenic rice plants for marker excision. (b) RT-PCR a...
Now that sequencing of the rice genome is nearly completed, functional analysis of its large number ...
<p>A) Photographs were taken of six week-old seedlings grown under greenhouse conditions. B) Picture...
The occurrence of genomic modifications in transgenic rice plants recovered from protoplasts and the...
The present study was designed to establish a qualitative detection method based on conventional and...
[[abstract]]With the completion of the rice genome sequencing project, the next major challenge is t...
Hybrid rice, grown in more than 50 % of the area in China, is be-coming popular in other Asian count...
Sequence-tagged sites (STSs) facilitate the conversion of a genetic map into a physical map, provide...
PCR is a powerful tool for the amplification of genetic sequences but sometimes, even though using a...
Early determination of transgenic plants that are homozygous for a single locus T-DNA insert is high...