Introduction
Recent genomic efforts on toxigenic and nontoxigenic
Aspergillus species have advanced
our understanding of the biology and
genetics of these filamentous fungi. However,
it is clear that these complex experiments
suffer greatly from the variability in the
quality of RNA between each replicate and it
is critical to establish a platform to isolate
high quality RNA for use in both microarray
and qRT-PCR. In that context we describe
here RNA isolation of A. parasiticus during a
simple carbohydrate shift. SPEXGENO 2010 高通量组织研磨机
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