Suggestions(5)
Exact(4)
Denaturing gradient gel electrophoresis (DGGE) was carried out for the various samples of firewater system (FWS) and the high intensity bands were sequenced to identify the predominant bacteria.
Some randomly chosen bands were sequenced to confirm the nature of the amplification products.
PCR was optimized for each primer pair, and amplified bands were sequenced to confirm deletions or insertions.
The predominant bands were sequenced to gain the closest bacterial relatives using the Basic Local Alignment Search Tool, and they were phylogenetically analyzed with MEGA 4.0 software [ 16, 17].
Similar(56)
A high number of clones from each band were sequenced to identify products with similar lengths which would not show up as separate bands on a gel.
Reactions that showed clear amplification bands were sequenced at the Genome Quebec Innovation Center (Montreal, Qc), using the specific primers (Table 1).
The maker bands were sequenced and converted to SCAR marker, this polymorphism in sequence was from an inserted/deleted (indels) mutation.
When the smaller bands were sequenced they were found to represent alternative splice variants.
The resulting bands were sequenced and their sequences were found to be identical to that of HMGA2.
PCR bands were sequenced with Gal4 reverse primer to confirm correct reading frame of the fusion mRNA.
The stained bands were sequenced on an Applied Biosystems 494 protein sequencer according to the manufacturer's instructions.
More suggestions(1)
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com