Software
MACSQuantify™ Software
control and analysis always at your fingertips
MACSQuantify Software enables reliable acquisition and easy and transparent analysis of flow cytometric data from multiparametric panels.
This intuitive software powers your MACSQuant® Analyzer to carry out high-performance flow cytometry and features easy-to-use Express Modes for automated and standardized data acquisition and subsequent analysis.
Additionally, MACSQuantify Software on your laptop offers the flexibility to analytically explore data and uncover insights wherever you are – because great ideas know no boundaries.
MACSQuantify Software is available as a stand-alone product or as an additional license for your existing software package.
FDA-compliant flow cytometry data with the MACSQuantify Software
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Automated calibration, compensation, and Express Modes
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Easy data management
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Compliance for electronic records and signatures
Features
Calibration and compensation
Automated processes like compensation and calibration ensure consistently high performance. MACSQuant Calibration Beads are specially developed for automated optimization of channel voltage settings.
Single stained cells or compensation beads can be used for fully automated compensation on up to eight colors via an 8x8 matrix. See how simple automated fluorescence compensation can be. Watch this video and download the application note.
Data management
Data files are automatically archived and are easily transferred to hard drive, USB stick, or a network drive. Additionally, all data are stored in a digital format that makes offline compensation easy.
Other file formats can be saved as well, including analysis templates (e.g. gating strategies) and FCS files for use by other programs. High-resolution charts can be easily printed or copied for immediate use in presentations or reports.
MACSQuant Express Modes
Make your life easier with Express Modes. This feature allows you to fully automate and standardize your experimental process.
From automated labeling of your sample to the analysis template, everything is done with little effort.
MACSQuantify 21 CFR Part 11 option
Enabling compliance for electronic records and signatures
The Subpart 11 of the Code of Federal Regulations Title 21 (21 CFR Part 11) defines the requirements for submitting electronic records to the FDA as well as the criteria for using electronic signatures. Our optional 21 CFR Part 11 software module of the MACSQuantify Software enables this by:
Time-stamped audit trails for all data files, which record the creation, modification and storage of the files
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Secure password-controlled user login that monitors inactivity time-outs, renewals, and attempted sign-in failures
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Controlled electronic signatures
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Optional: Connection to existing LDAP system