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Here we present a technology using sense oligonucleotides that bind to RNA binding proteins rather than RNA.
For evaluation designed progress and method was using sense course extract from medical database clinical electrocardiography record Physionet.
Messenger RNA analyses were performed by non-isotope in situ hybridisation using sense and antisense riboprobes produced from β subunits of LH and FSH cDNA clones.
The main idea in the proposed circuit is using sense amplifier for sensing the difference between voltages across the pull down network (PDN).
To this end we have developed a novel in situ hybridization approach in combination with immunoelectron microscopy, using sense and anti-sense RNA probes that are derived from total cellular or cytoplasmic poly(A+) RNA.
Immunoreactive (IR) GnRH neurons in the hypothalamus and LH cells in the adenohypophysis were localized by immunohistochemistry. Messenger RNA analyses were performed by nonisotope in situ hybridization using sense and anti-sense riboprobes produced from β subunits of LH cDNA clones.
The problem with quantifiers is inescapable for much that we routinely discuss using sense and reference.
In addition, we compute all cardiac images using SENSE [3] and GRAPPA [23] and 50% regular mask, which are the main methods in parallel MRI.
Tissue sections cut at 7 µm were subjected to ISH by using sense or antisense probe as previously described [25].
mCerulean was amplified by PCR using sense primer 5'-TATATCCGGAGATATCATGGTGAGCAAGGGCGAGGAG-3' and antisense primer 5'-TATAGAATTCTTTGTACAGCTCGTCCATGCCGA-3'.
In situ hybridization using sense RNA probe (Fig. 1G) and immunocytochemistry without LH primary antiserum (Fig. 1H) served as controls.
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