Abstract:More and more functional genomics laboratories are willing to invest in robotic workstations due to the higher throughput liquid-handling intensive nature of the work. In this report, the features of robotic workstations important for functional genomics are discussed. Workstations for functional genomics are useful for replication of clone sets, PCR and sequencing set-up and clean-up, hit picking, gel loading, and nucleic acid purification procedures. Workstations not only increase throughput, but also ensure… Show more
“…Use of such molecular approaches often results in a large library size which must be screened to identify potential hits. Developments in associated fields have promoted substantial advancement in our ability to access the biodiversity pool by using automated high‐throughput screening platforms ( Betton, 2004 ; Bradbury, 2004 ; Ho et al ., 2004 ; Lafferty and Dycaico, 2004 ; Lorenz, 2004 ; Pajak et al ., 2004 ). This significantly improves the ability to not only access a number of novel enzymes but also impacts the speed with which they are screened.…”
SummaryDevelopments in biocatalysis have been largely fuelled by consumer demands for new products, industrial attempts to improving existing process and minimizing waste, coupled with governmental measures to regulate consumer safety along with scientific advancements. One of the major hurdles to application of biocatalysis to chemical synthesis is unavailability of the desired enzyme to catalyse the reaction to allow for a viable process development. Even when the desired enzyme is available it often forces the process engineers to alter process parameters due to inadequacies of the enzyme, such as instability, inhibition, low yield or selectivity, etc. Developments in the field of enzyme or reaction engineering have allowed access to means to achieve the ends, such as directed evolution, de novo protein design, use of non‐conventional media, using new substrates for old enzymes, active‐site imprinting, altering temperature, etc. Utilization of enzyme discovery and improvement tools therefore provides a feasible means to overcome this problem. Judicious employment of these tools has resulted in significant advancements that have leveraged the research from laboratory to market thus impacting economic growth; however, there are further opportunities that have not yet been explored. The present review attempts to highlight some of these achievements and potential opportunities.
“…Use of such molecular approaches often results in a large library size which must be screened to identify potential hits. Developments in associated fields have promoted substantial advancement in our ability to access the biodiversity pool by using automated high‐throughput screening platforms ( Betton, 2004 ; Bradbury, 2004 ; Ho et al ., 2004 ; Lafferty and Dycaico, 2004 ; Lorenz, 2004 ; Pajak et al ., 2004 ). This significantly improves the ability to not only access a number of novel enzymes but also impacts the speed with which they are screened.…”
SummaryDevelopments in biocatalysis have been largely fuelled by consumer demands for new products, industrial attempts to improving existing process and minimizing waste, coupled with governmental measures to regulate consumer safety along with scientific advancements. One of the major hurdles to application of biocatalysis to chemical synthesis is unavailability of the desired enzyme to catalyse the reaction to allow for a viable process development. Even when the desired enzyme is available it often forces the process engineers to alter process parameters due to inadequacies of the enzyme, such as instability, inhibition, low yield or selectivity, etc. Developments in the field of enzyme or reaction engineering have allowed access to means to achieve the ends, such as directed evolution, de novo protein design, use of non‐conventional media, using new substrates for old enzymes, active‐site imprinting, altering temperature, etc. Utilization of enzyme discovery and improvement tools therefore provides a feasible means to overcome this problem. Judicious employment of these tools has resulted in significant advancements that have leveraged the research from laboratory to market thus impacting economic growth; however, there are further opportunities that have not yet been explored. The present review attempts to highlight some of these achievements and potential opportunities.
“…Transfer devices are typically part of larger platforms called liquid handling workstations that are designed to automate routine liquid handling tasks such as reagent dispensing, serial dilutions, and microplate replication (Lorenz, ). Some workstations may have more than one transfer device on the same workstation, such as an 8‐channel and a 96‐channel pipettor.…”
“…A continuing demand for increasing throughput has scaled biological assay procedures into 96-, 384-, and 1536-well formats. [2][3][4][5][6] This, of course, requires a miniaturization of the assay volume: a single assay volume typically was in the range of 250 µL in 96-well microplates by 1995; in 2003, the same assay volume ranged from 50 to 2 µL. 4 Today, 384-well or even 1536-well microplates are state of the art, with assay volumes moving down to the nanoliter range.…”
We present a noncontact liquid dispenser that uses a disposable cartridge for the calibration-free dosage of diverse biochemical reagents from the nanoliter to the microliter range. The dispensing system combines the advantages of a positive displacement syringe pump (responsible for defining the aliquot's volume with high accuracy) with a highly dynamic noncontact dispenser (providing kinetic energy to detach the liquid from the tip). The disposable, noncontact dispensing cartridge system renders elaborate washing procedures of tips obsolete. A noncontact sensor monitors the dispensing process to enable an online process control. To further increase confidence and reliability for particularly critical biomedical applications, an optional closed-loop control prevents malfunctions. The dispensing performance was characterized experimentally in the range of 0.25 to 10.0 µL using liquids of different rheological properties (viscosity 1.03-16.98 mPas, surface tension 30.49-70.83 mN/m) without adjusting or calibrating the actuation parameters. The precision ranged between a coefficient of variation of 0.5% and 5.3%, and the accuracy was below ±10%. The presented technology has the potential to contribute significantly to the improvement of biochemical liquid handling for laboratory automation in terms of usability, miniaturization, cost reduction, and safety.
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