BEVERLY, Mass., March 11, 2019 (GLOBE NEWSWIRE) -- LexaGene Holdings Inc. (OTCQB: LXXGF; TSX-V: LXG) (the “Company”), a biotechnology company that
develops genetic analyzers for pathogen detection and other molecular markers, announced today that Dr. Jack Regan, LexaGene’s CEO
and Founder, was invited by the Food Safety and Inspection Service (FSIS), an agency of the United States Department of Agriculture
(USDA), to present a seminar on the benefits of using LexaGene’s LX technology to help detect contaminated food items and prevent
recalls.
Invited guests of this seminar include individuals representing multiple federal agencies such as the Food and Drug
Administration (FDA), the Animal and Plant Health Inspection Service (APHIS), the Centers for Disease Control and Prevention (CDC),
the Environmental Protection Agency (EPA), the National Institute of Food and Agriculture (NIFA), the Food & Nutrition Service
(FNS), the Agricultural Research Service (ARS), and the Agricultural Marketing Service (AMS).
Dr. Regan’s presentation on using rapid genetic analysis for automated pathogen testing in the food industry will be given as
part of the FSIS Science and Technology Seminar Series on June 19, 2019, from 1-2 pm EDT at Patriots Plaza III in Washington, DC.
The FSIS Seminar Series fosters information exchange between FSIS personnel and professionals in public health, food science and
technology, microbiology, risk assessment, infectious disease, veterinary medicine and other related sciences.
Dr. Jack Regan, LexaGene’s CEO and Founder, states, “I’m honored to be selected by the USDA to present on this topic. I
look forward to sharing my knowledge and passion on the advantages of using LexaGene’s technology to dramatically improve food
safety.”
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About LexaGene Holdings Inc.
LexaGene is a biotechnology company commercializing the very first easy-to-use, fully automated, genetic analyzer that
is open-access. The open-access feature empowers end-users to target any genetic sequence of interest, whether of pathogen or
human origin. To take advantage of the open-access feature, end-users simply need to load their own real-time PCR assays onto
the instrument to customize their tests or run validated assays the company is developing. LexaGene’s analyzers offer
excellent sensitivity, specificity, and breadth of pathogen detection while returning results in about 1 hour. The company expects
to sell its technology in the food safety and veterinary diagnostics markets, as well as to markets that need easy-to-use
customized testing such as biotechnology and pharmaceutical companies, academia, and institutions performing water quality
monitoring, aquaculture pathogen surveillance, and others.
Media Contacts
Nicole Ridgedale
Director of Corporate Marketing, LexaGene
800.215.1824 ext 206
nridgedale@lexagene.com
Investor Relations
Jay Adelaar
Vice President of Capital Markets, LexaGene
800.215.1824 ext 207
jadelaar@lexagene.com
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This news release contains forward-looking information, which involves known and unknown risks,
uncertainties and other factors that may cause actual events to differ materially from current expectation. Important factors --
including the availability of funds, the results of financing efforts, the success of technology development efforts, the cost to
procure critical parts, performance of the instrument, market acceptance of the technology, regulatory acceptance, and licensing
issues -- that could cause actual results to differ materially from the Company's expectations as disclosed in the Company's
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extent required by law, to update or revise any forward-looking statements, whether as a result of new information, future events
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