University of Michigan
LSI ConnectionContact UsFacebookYouTube
LSI Search

Instrumentation

On-site XRay Facility

LSI 3358

The on-campus X-ray facility includes two X-ray diffraction systems.

  • Two Rigaku RU-300 copper rotating anodes equipped with Raxis IV dual imaging plate detectors
  • High Flux confocal optics (Molecular Structures Corp.)  
  • X-Stream cryo-cooling system
  • Linux computers for data collection

LS-CAT Synchrotron Beamlines

 

 UM is a member of LS-CAT, a consortium of academic and research institutions that operates a multi-beamline facility located at Sector 21 of Argonne National Laboratory's Advanced Photon Source. This facility consists of four experimental stations for X-ray crystallography with insertion device sources.  The primary station, 21-ID-D, is fully MAD capable and is tunable from 5–20 keV.  The 21-ID-F and 21-ID-G stations are at fixed energy (12.67 keV) and are suitable for selenium SAD experiments.  The fourth station, 21-ID-E, is planned to be tunable for selenium and bromine MAD. Each station is equipped with state-of-the-art diffractometers, robotic sample changers, and large-area CCD detectors.  Beam diameters of 5 to 50 microns are available.  Additionally, mail-in and remote access services are available.

 Crystallization Rooms

The CSB has two environmental rooms (4 °C and 20 °C) adjacent to the wet lab that are used for crystal growth. Each room is equipped with stereomicroscopes for crystal viewing.

Gryphon Crystallization Robot

The Gryphon crystallization robot dispenses drop volumes as low as 100 nanoliters. Its array of 96 glass syringes delivers up to 100 uL of precipitant simultaneously.

 

Desktop Minstrel

 

 The Desktop Minstrel is a stand-alone automated crystallization imaging system.  The Minstrel can accommodate all sitting drop crystallization plate types as well as hanging drop plates when a specific drop format is followed. Picture clarity comes from the incorporation of a 10 megapixel digital camera with auto focus and multi-slice image stitching to obtain a best view image. The system utilizes programmable LED lighting, which has a negligible heat load with automated polarization.  

Desktop Minstrel Interface

Images are captured and stored in an oracle database that can be viewed from the computer or through a secured login over the web. The plates are bar coded and organized into projects for easy book keeping. All vital information for an experiment can be stored in the database. This system aids users in developing a more uniform scoring routine. One just needs to click on a preset description to score the drop.  A color-coded outline will then appear around the picture of the drop for easy recall. In addition, the optimization head of the program will automatically design a 96 well optimization screen based on experimental conditions from multiple drops.]

 Protein Purification Facility

The CSB provides facilities to purify 1 – 100 mg proteins. In the facility, there is a
fermentation room with multiple variable temperature shakers for both large- and small-
scale fermentation, and a French press, sonicator and microfluidizer for breaking cells.
The large wet lab has two FPLCs (Acta Purifier-10 FPLC and an Academic FPLC from
Pharmacia) equipped with a variety of ion exchange, gel filtration and affinity
columns.

 

High-Throughput Protein Lab

Located in LSI 3238

Equipment in the HTP Lab

 The bacvulovirus process has been a “black box” in that quantitation of DNAs for input and titering of virus produced have been labor intensive, time-consuming and often unreliable.  Thus it is quite difficult to trouble-shoot problems of poor protein production or changes in detected expression level. Because the insect cell/baculovirus expression process typically requires 5-6 weeks, this is a large investment of time and resources without any guarantee of success.  By applying new tools, such as QPCR, the process becomes more transparent; the success rate can be increased enabling high-throughput methods.  Applications for QPCR in the baculovirus process include quantitation of specific DNAs in complex mixtures, development of transfection protocols with optimal efficiency, and quantitation of virus concentration in several hours as opposed to seven days for traditional titering methods.  HTP Lab equipment and protocols for doing this will be available to interested LSI users by contacting HTP staff for access and training.

MagNA Pure

The Roche MagNA Pure Compact unit automates nucleic acid isolation from tissues or other natural sources.  We will use this instrument to purify DNA from recombinant baculovirus.  The MagNA Pure will accept eight samples at a time and deliver QPCR-quality nucleic acid template in 30 minutes.

 

 Lightcycler

 

The Roche Lightcycler 1.5 system is a real-time, quantitative PCR instrument. QPCR monitors the incorporation of fluorescent label into the PCR product or release of label from degraded detection oligos during each cycle of PCR.  The incorporation of label or release of label over time is compared against standard curves and used to detect and also quantitate the amount of specific nucleic acids in a sample.   

 

 

Biomek FX

The Biomek FX liquid-handling robot is the workhorse of the High-Throughput Protein Lab. It allows rapid and precise execution of experimental steps in high-throughput cloning and expression optimization. The dual-arm Biomek has a 96-channel pipetting head for fast transfer of volumes up to 250 uL. A gripper for moving labware is integrated with the 96-channel head. The second arm of the Biomek has a pipettor with 8 individually controlled channels for transfer of volumes up to 1 mL.

Caliper Labchip 90

The Caliper Labchip 90, pictured here, is a high-throughput replacement for PAGE analysis of protein and DNA samples. The instrument is based on a microfluidic chip. Samples are introduced in a 96- or 384- well plate, and separated proteins or DNAs are detected by laser-induced fluorescence. The separation data can be displayed either as an electropherogram showing analyte peaks or formatted as a virtual gel image. The unit allows for easy switching between DNA and protein sample analysis through selection of several pre-configured assays. The sensitivity of this system is comparable to coomassie-stained gels but the labor and time involved in sample preparation and processing is considerably less.

Updated March, 2011

Science Design

 
RSS Feed for LSI     Contact LSI    |    Site Map    |    LSI Intranet    |    University of Michigan
© 2013 Regents of the University of Michigan