EPARATED RAGMENTS HOICE OF UFFER OLTAGE TAINING OLUTION E. M AINTENANCE OF F. R & A EPLACEMENT ARTS CCESSORIES QS-710 A CCESSORY TEMS AND EPLACEMENT ARTS QS-710 C OMBS G. R IBI P ELATED RODUCTS H. R IBI C 12-14...
AFETY NFORMATION Important Safety Information! Please read this manual carefully before operating your new IBI QS-710 unit. This manual contains important operating and safety information. To best use the product, please read the entire manual carefully prior to use. To avoid possible injury, this product should only be used for its intended purpose.
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PERATING NSTRUCTIONS Your new QS-710 Quick Screen Horizontal Unit is cleaned and wiped prior to packaging; however, components should be washed in warm soapy water prior to use in the laboratory. A mild dish wash- ing liquid, like Joy, works well.
4.) Add ethidium bromide (IB40075) to the diluted electrophoresis buffer to a final concentration of 0.5μg/ml. NOTE: The addition of ethidium bromide to both the gel and the running buffer will result in maximum detection levels by providing high levels of sample fluorescence with an evenly low level of background.
The following protocol will make 50ml of a 1.5% agarose gel containing 1X MOPS [3-(N- Morpholino)-Propanesulfonic Acid]-Acetate-EDTA (MAE) buffer and 2.2M formaldehyde, result- ing in a 7.5mm thick gel: 1.) Weigh out 0.5gm of agarose, and place into a 125ml flask. 2.) Add 43.5ml of DEPC (or acetic anhydride) treated water.
EMOVING THE 1.) When the gel is solidified and fully opaque, carefully remove the comb with a gentle wiggling, upward motion. If the comb is difficult to remove or if a low percentage gel is being used, overlay the comb area with a small volume of 1X electrophoresis buffer to preserve the integri- ty of the wells.
1.) The QS-710 is designed for quick screen electrophoresis. The maximum suggested applied voltage for the electrophoresis of DNA in agarose gels using the QS-710 is 100V. In a 1% TBE gel, this translates into a run time of approximately 1/2 hour. Lower voltages may be used, of course, and as a general rule, a 50V run will take twice as long as a 100V run.
2.) Follow the sample migration into the gel using the loading dye as an indicator. (See “Choice of Buffer” for the Sample Loading Buffer recipe) Allow the samples to migrate until the fragments have separated, normally until the bromophenol blue dye front has migrated 3/4 of the way down the gel.
8.0 OLTAGE The QS-710 is designed for rapid electrophoresis with moderate resolution. Suggested voltage is 100V for a 30 to 60 minute run. Higher voltages may be used to decrease run time, however, the volt-hours should remain constant. One should not exceed 200 volt-hours without changing the buffer in the unit.
0.8mm by 12-tooth combs, power cords, and manual SH-300 IBI 300V Power Supply (300V / 400mA / 120W) The SH-300 has constant voltage or constant current capability, memory settings, and a LED display. Comes complete with power supply, 120V grounded power cord, and manual.
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H. R IBI C ELATED ERTIFIED EAGENTS IB01010 6X Loading Dye IB01015 5X RNA Gel Loading Dye Kit 100RxN IB01020 10X TBE Pouch 1 Pouch IB01030 25X Tris-Acetate EDTA Buffer Pouch 1 Pouch IB74020 Acridine Orange 25gm IB70016 Acrylamide:Bisacrylamide, 29:1...
IBI Scientific to the customer, whether based on contract, tort, or any other legal theory. In no such event shall IBI Scientific be liable for dam- ages which exceed the purchase price of any products.