Skip to main content
Premium Trial:

Request an Annual Quote

Labcyte Closes $5.3M in Financing

NEW YORK (GenomeWeb News) – Labcyte has reeled in $5.3 million in Series D financing, which it plans to use to expand its acoustic low-volume liquid handling systems, the company said on Tuesday.

The new funding included backing from new investor GE Ventures' Heatlhymagination fund, and current investors, including Abingworth, Alloy Ventures, Cross Atlantic Partners, Delphi Ventures, H&Q Healthcare Investors, and H&Q Life Sciences Investors.

Sunnyvale, Calif.-based Labcyte said its acoustic systems enable the transfer of very low volumes of liquids without the use of pipettes, lowering costs and reducing errors, and provide the capability to miniaturize assays, which can boost throughput and productivity.

"Our systems are being employed to further personalized medicine with multiple applications in genomics, proteomics, diagnostics and cell health," Labcyte CEO and President Mark Fischer-Colbrie said in a statement.

"Closing the funding will further enable us to add to our product lines and accelerate our growth," he said.

The Scan

Positive Framing of Genetic Studies Can Spark Mistrust Among Underrepresented Groups

Researchers in Human Genetics and Genomics Advances report that how researchers describe genomic studies may alienate potential participants.

Small Study of Gene Editing to Treat Sickle Cell Disease

In a Novartis-sponsored study in the New England Journal of Medicine, researchers found that a CRISPR-Cas9-based treatment targeting promoters of genes encoding fetal hemoglobin could reduce disease symptoms.

Gut Microbiome Changes Appear in Infants Before They Develop Eczema, Study Finds

Researchers report in mSystems that infants experienced an enrichment in Clostridium sensu stricto 1 and Finegoldia and a depletion of Bacteroides before developing eczema.

Acute Myeloid Leukemia Treatment Specificity Enhanced With Stem Cell Editing

A study in Nature suggests epitope editing in donor stem cells prior to bone marrow transplants can stave off toxicity when targeting acute myeloid leukemia with immunotherapy.