Life Technologies Corporation

Life Technologies Holdings Pte Limited

Wescor Inc.

Kevin M Mullen

Scott Rickes

Sean Zimmerman

Christopher D Brau

Joshua Mead

Mio Ling

Woon Liang Soh

Alessandra Barbosa

Jordan Cobia

Harmon Cosme Sicat, Jr

Barry O Stokes

Wei Fuh Teo

Patti A Nelson

Harmon Jr Cosme Sicat

Kok Shyong Chong

Han Wei

Randal P Holman

Syed Muhammad Baber Ali

Display screen with graphical user interface for fluid mixing apparatus

The present set of embodiments relate to a system, method, and apparatus controlling a cell culture media mixing system. The control system includes an integrated control unit capable of controlling a broad ranges of peripheral devices commonly used in bioproduction through a graphical user interface displayed on a touch sensitive screen. The bioproduction system is designed to be highly customizable through process modification and recipe creation by user with little or no knowledge of programming and is capable of controlling a wide variety of devices using a single unit. The bioproduction system allows for auto-detection, auto-calibration, and automatic of device related processes into a bioproduction workflow.

Control system and method for a fluid mixing apparatus

Display screen with graphical user interface for fluid mixing

A cytocentrifuge sample chamber includes a sample receiving well to receive and hold a sample to be centrifuged and a sedimentation chamber adjacent a microscope slide upon which cells and/or other sediment material in the sample is to be deposited. A passage, such as a spillway, connects the sample receiving well and the sedimentation chamber, so that sample flows from the sample well under the influence of centrifugal force as centifugation begins into the sedimentation chamber where the sample is forced by centrifugal force against the microscope slide leaving a vacant space at the inner end of the sedimentation chamber. Sedimentation of the sample takes place against the microscope slide. When centrifugation ends, the liquid components of the sample flow back into the vacant space in the sedimentation chamber and can be removed from the vacant space at the inner end of the sedimentation chamber through a removal chamber. This avoids contamination of equipment and users and allows a secondary centrifugation to take place.

Large area cytocentrifuge sample chamber

Growing community of inventors

Smithfield, UT, United States of America

Kevin M Mullen