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First, a periodic parity relation based full decoupling residual generator with a periodic varying parity vector is designed.
The weight vector is designed based on the relationship of the magnitude difference between the two optimization objectives.
One weight vector is designed to be calculated in conjunction with the other through an iterative procedure.
First, transmission beamforming vector is designed to achieve the SEE maximization subject to the constraints of transmission power, minimum secrecy rate threshold and harvested energy threshold.
The Lpp OmpA vector is designed for use in the gram-negative bacterium Escherichia coli; the rationale for its dibrid form stems from the architecture of the E. coli envelope and the properties of the major Lpp and OmpA proteins.
This vector is designed to allow dual transcription of therapeutic factors, such as cytotoxic proteins, short hairpin RNAs or combinations, in the nucleus or cytoplasm of eukaryotic cells, with this expression sustained by an autocatalytic positive-feedback loop.
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The Bacillus subtilis GenoMe (BGM) vector was designed as a versatile vector for the cloning of giant DNA segments.
Therefore, a new expression system based on the pET26b vector was designed and a library was constructed.
The vector was designed such that it could be reused for two consecutive rounds of recombination to target both alleles.
Each vector was designed and constructed to contain two araC-pBAD inducible promoter systems for tight control over gene expression.
A lentivirus-based RNA interference (RNAi) vector was designed, synthesized and transfected into CFPAC-1 cells to inhibit EphB2 expression.
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CEO of Professional Science Editing for Scientists @ prosciediting.com