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Significant industrial benefits include reduced growth of scale, reduced agitator sedimentation bogging risk and improved reagent mixing.
The mutant protein, because of its improved stability and strengthened lattice interactions, thus provides a significantly improved reagent for use in structure-based drug design for this important disease target.
The frequency of such false negatives can be reduced by improved reagent design and using multiple, independent RNAi reagents per gene [ 6, 7].
The FLT3L-FC protein produced in vivo spontaneously homodimerized to enable effective FLT signaling and the FC-domain enhanced its plasma half-life, providing an improved reagent and method to boost DC numbers.
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Thus, improved reagents for nucleofection in the present study will largely reduce the cost for high efficiency of nucleofection.
To decrease reagent cost and improve reagent durability, we set the hard constraint that RNA probes and amplifiers be replaced by new DNA probes and amplifiers engineered to be suitable for use in situ.
Having completed development and validation of the first-generation HCR in situ amplification technology, we set out to improve reagent performance, cost, and durability by revisiting key engineering challenges and decisions.
Flotation rates and recoveries are improved and reagent needs are lowered.
Similar results were found using the recently improved MiSeq reagent kit for extended PE reads of 250 bp with 87.5% of read 1 bases and 75.7% of read 2 bases at >Q30.
We found that incorporation of a sulfur atom into the cyclooctyne ring improves overall reagent stability but also reduces azide cycloaddition kinetics.
First, patterned reagents provide improved control over dry reagent rehydration, allowing customized rehydration profiles.
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CEO of Professional Science Editing for Scientists @ prosciediting.com