Transformation efficiency depends on the quality of the competent cells. Make sure that cells were immediately frozen after preparation and stored at ≤ 80 °C. Please also note that for…
No. All our Toolbox 2.0 plasmids (except the positive control plasmid P70a-deGFP that comes with the myTXTL kit are meant for plasmid amplification in E. coli only. The degree of…
Our team has optimized processes for library preparation, target capture, sequencing, and bioinformatics, allowing us to execute projects of any size.
Batch-to-batch variation can cause varying levels of TXTL inhibitor contamination present in the plasmid solution. Please follow our recommendations on how to prepare template plasmid DNA for TXTL reactions in…
Yes! Our expert myReads team provides a range of in-house NGS services, including library preparation, target capture with myBaits, high-throughput sequencing, and optional bioinformatics analysis. Visit the Sequencing Services page…
…over 1000 segregating variants with zero missing data for 92% of species and demonstrate that Angiosperms353 markers contain sufficient variation to estimate pairwise nucleotide diversity (π)—typically between 0.002 and 0.010,…
…accommodate the species previously placed in Parmotrema subgen. Crespoa. This study demonstrates the power of reduced genome-scale data sets to resolve phylogenetic relationships with high support. Due to lower costs,…
Contact us using the form below. First name:* Last name:* E-mail:* Company Name:* Address 1: City: State: Zip Code: Country: – Afghanistan, Islamic State Albania Algeria American Samoa Andorra, Principality…
…(Silur). Six thousand sequence baits were designed to target Dic2 vs. Silur polymorphisms discovered in a previous RNAseq study. These baits were exposed to genomic DNA of the RIL population….
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