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LabAutomation 2006 - SLAS

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MP81<br />

Steven Wilson<br />

Joint Genome Institute<br />

Walnut Creek, California<br />

sewilson@lbl.gov<br />

Where Laboratory Technologies Emerge and Merge<br />

Co-Author(s)<br />

Paul Richardson<br />

Feng Chen<br />

Jamie Jett<br />

Nancy Hammon<br />

Duane Kubischta<br />

Diana Lawrence<br />

Implementing the Agencourt SprintPrep384 Protocol at JGI<br />

SprintPrep DNA isolation is a process that allows large fragments of DNA and vectors to be isolated from the host E. Coli cell. Agencourt<br />

has developed SprintPrep reagents and semi-automated methods for performing the necessary protocol. Last year, JGI implemented a 96<br />

well SprintPrep method. This year, JGI has made the 384 SprintPrep method virtually user-independent.<br />

Moving from the 96 well fosmid isolation method to the 384 well format has led to cost savings due to reagent reductions and a doubling in<br />

sequencing throughput. The increase in throughput will lead to an increase in sequencing depth and data confidence.<br />

This work was performed under the auspices of the US Department of Energy’s Office of Science, Biological and Environmental Research<br />

Program and the by the University of California, Lawrence Livermore National Laboratory under Contract No. W-7405-Eng-48, Lawrence<br />

Berkeley National Laboratory under contract No. DE-AC02-05CH11231 and Los Alamos National Laboratory under contract No. W-7405-<br />

ENG-36.<br />

MP82<br />

Lester Wong<br />

Alberta Agriculture<br />

Edmonton, Alberta, Canada<br />

lester.wong@gov.ab.ca<br />

Co-Author(s)<br />

John Wu<br />

Evelyn Bowlby<br />

Alberta Agriculture<br />

An Automated High-Throughput Screening Enzyme Linked Immunosorbent Assay for<br />

Johne’s Disease Antibodies in Bovine Serum<br />

One manual Mycobacterium paratuberculosis enzyme linked immunosorbent assay (ELISA) was fully automated using an Automation<br />

Workstation System designed based on a modular approach. This high throughput screening configuration consisted of a Beckman<br />

Coulter hybrid Biomek ® FX liquid handling system integrated with a Molecular Devices Spectramax ® microplate reader, a Biotek ® ELx405<br />

microplate washer and a Kendro Cytomat ® 6000 hotel. The integrated system function was programmed with an IBM computer using the<br />

SAMI ® software. This setup was housed in a Class 2 Biosafety Cabinet. The two assays were validated according to the requirements of<br />

the ISO/IEC 17025 standard. Starting in 2001, the test scope has received ISO accreditation from Standard Council of Canada. We have<br />

been approved by the United States Department of Agriculture to perform Johne’s disease serology using the ELISA since 1998. The<br />

productivity of full automation of this test has been discussed. The performance characteristics, such as the kappa quotient, identity score,<br />

test sensitivity and specificity, positive and negative predictive values of 2 commercial manual tests (IDEXX and BIOCOR) were evaluated.<br />

143

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