Tulin and Cross TS-Lethal Collection
BLY2 mt+
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
cdka-1 mt- [Cross ts301]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
cdka-1 mt+ [Cross ts301]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
dd-1-p
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div1-3 mt- [Cross ts68]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div1-4 mt- [Cross ts133]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div13-1 mt- [Cross tsm18]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div13-1 mt+ [Cross tsm18]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div13-2 mt- [Cross ts187]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div13-2 mt+ [Cross ts187]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div13-3 mt- [Cross ts198]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div13-3 mt+ [Cross ts198]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div14-1 mt- [Cross ts147]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div14-1 mt+ [Cross ts147]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div14-2 mt- [Cross ts195]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div14-2 mt+ [Cross ts195]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div14-3 mt- [Cross TL7-41]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div14-3 mt+ [Cross TL7-41]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div15-1 mt- [Cross ts121]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div15-1 mt+ [Cross ts121]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div15-2 mt- [Cross tsm15]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div15-2 mt+ [Cross tsm15]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div15-3 mt- [Cross TL21-51]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div15-3 mt+ [Cross TL21-51]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div16-1 mt- [Cross ts66]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div16-1 mt+ [Cross ts66]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div16-2 mt- [Cross ts305]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div16-2 mt+ [Cross ts305]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div16-3 mt- [Cross ts322]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
div16-3 mt+ [Cross ts322]
$30.00
$30.00
From Fred Cross, The Rockefeller University, May 2016
This collection of ts-lethal mutations was generated by UV mutagenesis. The location and probable identity of the causative mutation was determined by bulked segregant sequence analysis (Tulin and Cross 2014). Information is provided identifying the most likely causative mutation. All strains were backcrossed at least once to WT. It is highly recommended that the co-segregation of the indicated mutation (for example by allele-specific PCR) and ts-lethality be confirmed as a first step, before carrying out additional experiments. As noted in the publication, the map location of the causative mutation is highly likely to be correct. Identification of the causative mutation itself involves less certain inference.
For allele-specific PCR, we have had a very high success rate with the competitive amplification assay using oligos designed according to the principles described in Onishi, Pringle and Cross 2015.
Tulin F, Cross FR (2014) A microbial avenue to cell cycle control in the plant superkingdom. Plant Cell. 26(10): 4019-38
- 1
- 2
- 3
- …
- 13
- Next Page»