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Please use this chart to choose the ideal size cooler for your shipment, based on number of days in transit. Note that larger samples require larger shipping coolers, because the amount of dry ice will be reduced.

This is the protocol that accompanies our 2011 article: Plate-based transfection and culturing technique for genetic manipulation of Plasmodium falciparum, by Florencia Caro and Matt Miller, published in Malaria Journal.
Plasmodium plate based transfection protocol

This is the raw sequence data that accompanies our 2011 paper Temporal Analysis of the Honey Bee Microbiome Reveals Four Novel Viruses and Seasonal Prevalence of Known Viruses, Nosema, and Crithidia This data was generated on the Illumina platform and consists of a lane of paired end 65nt read files. Both Lake Sinai virus 1 and Lake Sinai virus 2 may be assembled from these reads. The file is large, consisting of a 4Gb zip compressed file.
Download raw sequence read archive (Warning: 4Gb zip file)

We are pleased to introduce MITOMI 2.0, a microfluidic platform and analysis pipeline for high-throughput measurement of transcription factor DNA sequence preferences and interaction affinities. Using a panel of 28 S. cerevisiae transcription factors, including 2 that were previously uncharacterized, we demonstrated the ability to comprehensively identify both high- and low-affinity target sequences and directly measure relative binding affinities. We hope that both the extensive data set presented here (including affinity information for each transcription factor binding to 1457 oligonucleotide sequences) and future use of this technique help elucidate the fundamental mechanisms by which transcription factors regulate gene expression.
Click here to download the raw Mitomi v2 data from the paper. (18Mb zip archive)