The phrase "analysis of the transformants" is correct and usable in written English.
It can be used in scientific or research contexts when discussing the examination or evaluation of transformed organisms or cells, typically in genetic studies.
Example: "The analysis of the transformants revealed significant changes in gene expression compared to the control group."
Alternatives: "examination of the transformants" or "evaluation of the transformants".
Quantitative Reverse Transcriptase Polymerase Chain Reaction (Q-RT-PCR) analysis of the transformants and wild-type controls showed that for plants transformed with 35S::PCN-miRNAd, one line (35S::PCN-miRNAd-4-1) had approximately two-fold increase of PCN transcript abundance relative to controls, while line 35S::PCN-miRNAd-4-3 had over twelve-fold increase in PCN transcript abundance (Fig. 4a).
Southern analysis of the transformants confirmed that pBT6 exists as an integration vector, and laeA integrated in the genome at random.
Sequence analysis of the transformants from the gene-replacement experiment confirmed that the INU1 ORF had been replaced by sequences encoding scFv; two of the resulting constructs were designated strains No. 6 (Km02-064) and No.7 (Km02-065) (Figs. 1b and 3b).
Microscopic analysis of the transformants revealed that CAS1-EGFP and CAS3-EGFP proteins were uniformly distributed throughout the cytoplasm of fast-growing, young hyphae, as well as old hyphae.
PCR analysis of the transformants showed the T-DNA was integrated in the chromosomes.
In addition, polysome analysis of the transformants showed less 5S rRNA and rbcL mRNA associated with ribosomes.
SKB carried out the light microscopic and SEM analysis of the transformant lines for GSQUA2.
The fatty acid analysis of the transformant yeast cells grown in galactose-containing medium showed the presence of a new fatty acid, which was not present either in the wild-type yeast or in the control cells transformed with the empty vector pYES2.
Enzymatic analysis of the transformant lysates showed that the strain expressing mutant BGLII exhibited weakened cellobiose hydrolytic activity, but produced some transglycosylation products, suggesting that the SNP in bgl2 strongly diminished cellobiase activity, but did not result in complete loss of function of BGLII.
Following transformation and analysis of the purified transformants by diagnostic PCR, several lxr3 deletion strains were identified.
The hybridization probe for the southern blot analysis of the TDR transformants was designed to consist of a single fragment containing FADO, TprC terminator, tef1 promoter and FAR sequence, originating from the previously constructed expression vector (Fig. 3a).
