The phrase "a pool of isolates" is correct and usable in written English.
It can be used in contexts related to biology, microbiology, or data analysis, where it refers to a collection of isolated entities or samples.
Example: "In our study, we examined a pool of isolates to determine their resistance to antibiotics."
Alternatives: "a collection of isolates" or "a set of isolates".
As self-medication and treatment delay were found to be major factors associated with SM, a strong involvement of drug resistance in the selection of a pool of isolates is suggested.
Furthermore the addition of a pool of isolates without clinical data allowed for a simulation of real life treatment scenario of an outpatient with UTI.
The authors postulated that other avirulence genes of M. oryzae may have the same behaviour and also be subjected to multiple translocations in the genomes and that this maintains a pool of isolates with the avirulence gene when selection is exerted so that it can be easily disseminated in populations when the selection is no more present.
In total 24 isolates were selected from a pool of 38 isolates that were used in the study from Rattei et al. [ 12] according to three stringent characteristics: 1) highest variety in geographical origin; 2) highest variety in anatomical origin; and 3) possibility to purely cultivate the pathogen.
Typing of suspected samples was performed by PCR [ 19] on a pool of four isolates having characteristic colony morphology on Columbia agar (shiny, grey, double-haemolytic colonies).
Thus, the inoculation of cattle with a pool of scrapie isolates of possibly various strains may have contributed to the heterogeneity in the molecular PrPres profiles observed in this study.
The American Chestnut Canker cDNA library was constructed from a pool of RNA isolated from canker tissues of several individuals of one genotype (BA69).
In this study aiming to obtain transcriptome sequences, next-generation sequencing was performed in a pool of mRNAs isolated from S. elaeagnifolium leaves and flowers.
The calibration curve was composed of serial dilutions of a pool of mRNA isolated from; HCV cells for measurement of HER1 and HER2 whereas HEC and KLE cells were used for HER3 and HER4, respectively.
A G. uralensis cDNA library was constructed from a pool of mRNA isolated from the vegetative organs of G. uralensis and was sequenced using the 454 GS FLX platform and Titanium regents.
Staining of the chromatin with the fluorochrome Ho gives the opportunity to identify within a pool of oocytes isolated from the antral compartment of the ovary those that may develop to term (SN) from those that certainly arrest development soon after fertilisation (NSN) [ 25– 28].
