Sentence examples for segregation of plants from inspiring English sources

Genetic segregation of plants with T-DNA inserts was completed in triplicate by recording T-DNA insertion and the number of surviving seedlings that geminated out of ~100 seeds growing in half-strength MS media containing 7.5 mg/L phosphinotricin or 50 mg/L kanamycin, followed by χ analysis.

We also reveal a group of co-conserved residues that closely associated with the segregation of plant OSCs.

Asymmetric transgressive segregation of plant height across the GPMx population can be observed – there were around 40 lines taller than Morex, but only about 10 shorter than Golden Promise.

Moreover, due to the strong segregation of plant maturity type in the C × E population, the use of younger tubers would introduce a strong bias, based on the variation in the physiological age of the tubers and thus gene expression.

Based on the segregation analysis of plants grown on antibiotic-containing plates, lines putatively homozygous for the T-DNA insertion were subjected to PCR analysis using T-DNA-specific (LBb1) and AtTIL-specific (RP) primers, and the resulting PCR fragments were sequenced to determine the precise insertion sites.

Segregation of homozygous plants carrying the T-DNA insertion was confirmed on genomic level by PCR, using the left border primer TL1 and the CAT8-specific reverse primer Crv: CCTATGATGTAGCTCATCAGCC. Lack of the transcript in cat8-1 was verified by RT-PCR using Crv and Cfw: CTCggtaccATGATCCCTGCTTCAATGGAG primers.

Histograms of the segregation of sesame plant height and related traits across three trial sites; Figure S7.

Given the segregation of the plant's progeny in regards to ACC resistance, we hypothesize the involvement of a genetic component in this resistance.

Segregation of the F2 plants fitted a 3 light purple: 1 white ratio except one plant that had purple flowers.

Homozygous single locus insertion lines were then isolated by following segregation of hygromycin-resistant plants in T2/T3 generations (Additional file 2).

Progeny were sprayed with glufosinate (40 micrograms ml -1 active ingredient: WipeOut, Nu-Gro IP Inc., Ontario) to test for herbicide resistance and resistant plants tested for segregation of hth mutant progeny plants.