Restriction of processing: Request that we restrict our processing of personal data if there is a dispute about the accuracy of the data; if the processing is unlawful; if the processing is no longer necessary for the purposes for which it was collected but is needed by you for the establish...
It is also possible to impose some type of scheduler restriction to either limit the maximum number of assigned DL subframes for each UE (e.g., to four or five) or limit the number of UEs that are simultaneously scheduled in each DL subframe. In that case, the bundling window length ...
The R select unit for R new may operate on any of the previous layers. R generation is independent of PS or FS processing, so, out-of-order R message generation imposes no any additional restriction on the architecture. Based on the desired hardware implementation objectives, for example, ...
The nucleic acids of the present invention provide for a simple way to generate fragments (e.g., truncations) of UspA1 or UspA2, UspA1-UspA2 fusion molecules (discussed above) and UspA1 or UspA2 fusions with other molecules. For example, utilization of restriction enzymes and nuclease in ...
R generation is independent of PS or FS processing, so, out-of-order R message generation imposes no any additional restriction on the architecture. Based on the desired hardware implementation objectives, for example, the number of pipeline stages required in a hardware implementation without stall...
pMalE-RT plasmids were derived from these initial constructs by PCR amplifying the RT ORF with primers that append restriction sites, and then cloning the PCR products into the corresponding sites of pMal-c2t (TeI4c RT, EcoRI and PstI sites; TeI4f RT, BamHI site; TeI4h* RT, BamHI ...
The C-prM-E cassette was also cloned into the lentiviral vector pLenti6/V5 vector (Invitrogen) using the above restriction sites to generate plasmid pLenti-C-prM-E. The prM-E construct was generated by PCR amplification of prM-E region spanning amino acids 105-795 using the Phusion high ...
“operably linked” refers to a DNA sequences being linked are contiguous and, in the case of a secretory leader, contiguous and in same reading frame. Enhancers do not have to be contiguous. Linking is accomplished by ligation at convenient restriction sites. If such sites do not exist, ...