Myra Liquid Handling System from Bio Molecular Systems

Description

The first liquid handling robot that can see!

Simplified solutions for laboratory processes including qPCR, NGS library prep, enzymatics and more.
High precision and accuracy pipette head with pressure based liquid level sensing.
Integrated camera to enable Myra to see what it has to do including one click position calibration.
Small footprint and low weight.
Easy to use software that is fully integrated with the Mic qPCR cycler.
UV light and HEPA filter as standard.

Product Specs
ItemMyra Liquid Handling System
CompanyBio Molecular Systems
Price Get Pricing
Catalog NumberMYRA-LHS50
Volume1 to 50 µL
Dimensions(WxDxH) 35 x 46 x 31 cm
QuantityEA
Electrical Requirements100 to 240 VAC, 50/60 Hz
Weight9 kg
Accuracy1 µL < 10%; 2 to 50 µL < 1%
CalibrationHigh precision camera
Precision1 µL < 10% CV; 2 to 50 µL < 1% CV
UV LampHigh intensity 70 mW 280 nm UV LED
ApplicationsqPCR, NGS library prep, drug discovery, and more

Specifications/Features

Position Control Closed loop, 100 micron resolution

Liquid Detection Pressure sensing

HEPA Filter 99.98% at 0.3 µm

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Bio Molecular Systems

Unit 5/3 Northward Street

Upper Coomera, QLD 4209

Australia

Company Profile

Website: www.biomolecularsystems.com

(1) Molecular Epidemiology and Assemblage Typing of Giardia duodenalis in School-Age Children Situated along the Southern Shoreline of Lake Malawi, MalawiThe American Journal of Tropical Medicine and HygieneSeptember 6, 2023John Archer, Lucas J. Cunningham, Alexandra Juhàsz, Sam Jones, Ffion Doull, James E. LaCourse, Bright Mainga, Peter Makaula, Sekeleghe A. Kayuni, Janelisa Musaya, et al.Molecular Systems, Upper Coomera, Australia). All real-time PCR assay plates were prepared using a Myra liquid handling system (Bio Molecular Systems, London, UK). A cycle threshold (Ct) value of ≤ 39 was deemed positive for infection

(2) Analytical sensitivity of a multiplex quantitative PCR for Toxoplasma gondii and Neospora caninumParasitology ResearchApril 1, 2023Marcus Truong, Jan Šlapeta(Table 1). All probes and primers were obtained from Integrated DNA Technologies (IDT, Australia). The Myra Liquid Handling System (Bio Molecular Systems, Australia) was used to prepare and multiplex all PCR reactions. All qPCRs were

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