TrayMix™ S4 Hybridization Station

Manufactured By: Arrayit

Manufacturer SKU: TMHS

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Product 3031-79

$36,974

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Details & Specs

Features and Benefits

TrayMix S4 Features and Benefits

More Information

Four independent hybridization chambers. Each chamber accepts one substrate slide for a total of 4 substrates per unit

Chambers can be launched simultaneously or set to run different protocols via the user-friendly graphical user interface

Up to 60 μl of sample can be introduced into each hybridization chamber through dedicated access port. Gaskets (black), on upper portion of the lid, are used to seal chambers.

Close ports prior to hybridization to prevent evaporation. System automatically delivers solutions into the 50 μl hybridization chambers when unit is programmed and substrates are in place.

TrayMix S4 Automated Hybridization Station Chaotic Advection Mixing

Chaotic advection mixing assures that all biomolecules in solution reaches every spot on the microarray via microfluidic pumps combined with a mixing loop. The extremely complex direction and speed of fluids created by the mixing loop creates a chaotic movement, a very efficient way to mix low volume liquids in the shortest period of time. The chaotic advection mixing method in the TrayMix S4 accelerates hybridization kinetics by up to 90% and increases sample yield.

Static versus Dynamic Microarray Hybridization

Probe concentration (0.1 µM)	Solution volume(µl)	Probe quantity (pmoles)	Method	Hybridization solution	Fluorescent Mean (a.u.)	CV
Static Hybridization	50	5	cover slip	homogenous	5500	0.33
Static Hybridization	500	50	TrayMix™ S4	homogenous	38500	0.56
Dynamic Hybridization	500	50	TrayMix™ S4	homogenous	11474	0.18
Dynamic Hybridization	500	50	TrayMix™ S4	non homogeneous	11823	0.17
Average fluorescence values and coefficients of variation (CVs) measured under different hybridization conditions (2 hours of hybridization).

Probe quantity (5 pmole)	Solution volume (µL)	Concentration (µM)	Method	Hybridization solution	Fluorescence mean (a.u.)	CV
Static hybridization	50	0.1	cover slip	Homogenous	5500	0.33
Dynamic hybridization	500	0.01	TrayMix™ S4	Non-homogeneous	6452	0.16
Average value for fluorescence and CV obtained with the same quantity of targets, both with and without agitation (2 hours of hybridization).

Dynamic advection mixing provides superior signal-to-noise ratios for microarray analysis. This image shows data obtained from two microarrays hybridized for two hours with a single-stranded CY3 labeled DNA probe complementary to allele a. Hybridizations were performed with 5 pmol of target under the traditional coverslip method and with the TrayMix™. All spot features were analyzed and compared to a reference background signal. Results comparing the mean signal to noise ratio of the fluorescent CY3 signals to the local background for allele a (black) and allele b (grey) of three experiments ± SD (Standard Deviation). These data show that the specific signal/noise ratio (allele a – black bars) is enhanced from 3.5 to 4.2, while the non-specific signal/noise ratio (allele b – grey bars) is slightly reduced under the dynamic hybridization conditions of the TrayMix S4.

Software Interface

The easy software interface of the TrayMix S4 streamlines and easily define the hybridization process. The software interface has three main functions:

Traces operations and generates reports in HTML format
Saves and loads protocols
Modifies system operation in all of the experimental steps including pre-hybridization, hybridization and washing

Hybridization Protocol of TrayMix S4

Set Pre-hybridization Time and Temperature
Set Hybridization Time and Temperature
Set Wash Parameters, program is ready to run!
Insert microarray slide and click proceed
Check the system is locked properly and port cap is properly closed.
Programmed Pre-hybridization Program Starts, gets the microarray at proper temperature and wets the microarray prior to adding the labeled sample
After complete Pre-hybridization and temperature is stabilized, remove air bubbles for the chaotic advection mixing-loop.
Air bubbles are automatically removed.
Inject sample with a volume of 30ul or 60ul, set volume and click proceed.
The mixing loop automatically compensates for the volume injected for hybridization.
Hybridization proceeds at set time and temperature with constant mixing.
Wash steps proceed automatically according to set program parameters.
When chamber is empty, microarray is removed from the system and dried in a microarray centrifuge.

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Laboratory-Equipment