Sponsor: EMD Millipore
Data presented in this webinar illustrates the value of live cell analysis at the single-cell level to identify differences in expression levels across populations of cells. The cells remain intact for downstream analysis. Our experts also discuss the use of SmartFlare RNA detection probes for the direct quantification of circulating miRNAs with rapid processing of blood plasma/serum, which is done without the use of enzymes. Using circulating miRNAs with established roles in cancer and quality control, we can accurately detect these miRNAs in plasma using a microplate fluorometer within an hour after plasma preparation.
On-demand recording is available here.
At the time of its
At the time of its announcement, I provided a summary of many problematic aspects of the Wolfe-Simon NASA study in a previous commentary in GenomeWeb's The Daily Scan. It can be viewed at the url:
http://www.genomeweb.com/blog/arsenic-yes-please
I agree with my University of British Columbia colleague Dr. Redfield that the far reaching conclusions of the Wolfe-Simon et al. paper are not sufficiently supported by the data.
Perhaps the quantity of
Perhaps the quantity of phosphate in Redfield's experiment was too high. If phosphate is available then the bacteria will incorporate phosphate into their DNA. They prefer phosphate to arsenate.
To claim that the bacteria are incapable of incorporating arsenate, the experiment should be set up so that they have no choice. Either they incorporate arsenate or they don't replicate their DNA.
Redfield's observation that the bacteria grew yet didn't incorporate arsenate implies that they did have a choice. And they chose phosphate which is no surprise.
This work does not refute Wolfe-Simon's findings.