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167

the velocity of the deformation- and this mechanical component can

sometimes be lost or ignored in certain experimental setups and tech-

niques. In fact, this viscous response may prove just as enlightening to

cell mechanics as the elastic response more commonly measured alone

until recently. This talk will discuss these important issues that must be

considered when AFM techniques are applied to cells and other biologi-

cal materials.

Speaker

Sophia Hohlbauch, Asylum Research, an Oxford Instruments Company

1:30 pm–3:00 pm

KinTek Corporation

Why You Should Fit Kinetic and Equilibrium Binding Data

Using Kintek Explorer Software

KinTek Explorer

software offers the fastest, most dynamic and robust

method of fitting kinetic or equilibrium binding data. Based on fast

numerical integration of rate equations, data are fit without the often-

inaccurate approximations needed to derive equations. Rather than fit-

ting data to extract “observed rates” or Eigenvalues, which must be then

interpreted in second step,

KinTek Explorer

yield rate and equilibrium

constants directly while accounting for both the rate and amplitude of

observable reactions. By modeling the experiments exactly as per-

formed, all details of the experimental setup are included, eliminating

errors in interpretation. Moreover, multiple experiments can be fit

simultaneously to a single unifying model. Fast dynamic simulation using

proprietary methods for numerical integration allows you to explore

parameter space and learn kinetics. Don’t be fooled by other vendors

pretending to do the same. Only

KinTek Explorer

offers such robust and

dynamic data fitting.

In this presentation, Professor Johnson will introduce the theory and

operation of the software to show you how easy it is to fit data to

any model you care to input. Examples of experiments that can

be fit include: transient and single turnover stopped-flow kinetics,

steady state kinetics, slow onset inhibition, equilibrium titrations, rapid-

quench-flow kinetics, temperature dependence, voltage-dependent

rate constants. In addition time-resolved absorbance or fluorescence

and pH-dependent spectra can be analyzed by singular value decom-

position to yield spectra and time- or pH-dependence of each spe-

cies. In addition to describing

KinTek Explorer’s

basic features, Dr.

Johnson will introduce new features and will be available to help

you to fit your own data. Learn about what you are missing in your

own data fitting. See

www.kintek-corp.com

for more information.

Speaker

Kenneth A Johnson, President, KinTek Corporation; Professor of

Biochemistry, University of Texas at Austin

3:30 pm–5:00 pm

Bruker Nano Surfaces

Advances in Live Super-resolution Imaging Using the Vutara

352 Microscope

Super-resolution microscopy has made a significant impact in the field of

biological imaging by enabling a ten-fold improvement in spatial resolu-

tion over traditional light microscopy techniques. Most of the imaging

has been so far targeted at fixed specimens with a few live cell applica-

tions. The Vutara 352 microscope has been engineered towards live-cell

imaging by enhancing spatial and temporal resolution in single molecule

localization super-resolution. The sCMOS detector in the Vutara 352

enables imaging at 800 fps at full ROI and at video frame rates at reduced

ROI. Two color simultaneous imaging can be applied in both super-res-

olution live cell and 3D particle tracking experiments. The biplane based

detection path enables imaging thicker samples such as whole mount

Drosophila and offers deeper penetration into tissues. The Vutara 352

also includes real time localization along with several statistical and live

cell analysis features for processing data. In summary, the Vutara 352

microscope is a powerful super-resolution imaging and analysis tool.

Speaker

Manasa Gudheti, Applications Scientist at Bruker – Fluorescence

Microscopy Business

5:30 pm–7:00 pm

Sutter Instrument

Scientists Empowering Scientists

Patch clamp electrophysiology has matured from a highly specialized

scientific technique to a recognized method used to address a variety

of experimental questions. Sutter Instrument introduces a highly flex-

ible, intuitive patch clamp instrumentation and software package that

enables the experimenter to quickly set up and perform routine tasks,

yet remains highly configurable to meet the demands of the experienced

electrophysiologist.

We will demonstrate how the IPA™ Integrated Patch Amplifier and

SutterPatch™ software can be used for a variety of commonly performed

assays, including the characterization of an ionic current and the record-

ing of synaptic events in tissue slices. We will also highlight how the IPA

and SutterPatch software provide easy access and flexibility to perform

and fine-tune the most challenging acquisition and analysis scenarios.

Building on the basic pipette pulling tutorials presented at the 2015 user

meeting and a mid-year webinar, we will further teach advanced tech-

niques that enable the user to create specialized pipette morphologies

for unique applications.

There will be plenty of opportunity for discussion with hosts and speak-

ers from the Sutter Instrument Tech Support Team.

Who should attend?

• Electrophysiologists who use amplifiers, micropipettes and micro-

manipulators for patch clamp, sharp electrode or extracellular

recordings.

• Researchers who perform microinjections, including nuclear trans-

fer, sperm injection and application of substances into cell cultures

or intact organisms.

Speakers

Jan Dolzer, Tech Support and Product Development, Sutter Instrument

Gregory Hjelmstad, Tech Support and Product Development, Sutter

Instrument