* Your assessment is very important for improving the workof artificial intelligence, which forms the content of this project
Download Mini-Gel Electrophoresis Unit for DNA, RNA and Protein
Survey
Document related concepts
Transcript
SUBSIDIARIES BELGIUM EUROGENTEC s.a. Tel. 04 372 74 00 Fax 04 372 75 00 FRANCE EUROGENTEC France s.a. Tel. 02 41 73 33 73 Fax 02 41 73 10 26 SWITZERLAND EUROGENTEC s.a. succursale de Genève Français: Tel. +32 4 366 61 00 Fax +32 4 264 07 88 Deutsch: Tel. +49 221 258 94 55 Fax +49 221 258 94 54 i-MUPID GERMANY EUROGENTEC Deutschland GmbH Tel. 0221 258 94 55 Fax 0221 258 94 54 THE NETHERLANDS EUROGENTEC Nederland b.v. Tel. 043 363 40 37 Fax 043 363 77 65 Ref. GEN-iMUPID-MANUAL-0803-V4 Mini-Gel Electrophoresis Unit for DNA, RNA and Protein Parc scientifique du Sart Tilman • 4102 SERAING • BELGIUM Tel.: +32 4 372 74 00 • Fax: +32 4 372 75 00 [email protected] • www.eurogentec.com Consumables Agaroses Molecular Biology Grade Small Fragments Nucleic acid length range > 1000 bp < 1000 bp Gelling temperature* 37 ~ 39 C 29 ~ 33 C Melting temperature 88 ~ 90 C Gel strength* 1500 g/cm2 Introduction _________________________________________3 Components _____________________________________ 4 - 5 Setup / warranty ____________________________________6 Instructions for use ___________________________________7 Set the i-Mupid __________________________________7 DNase or RNase activity DNA binding Electroendosmosis ND ND ND 0.1 ~ 0.2 0.06 ~ 0.14 0.1 % Buffers____________________________________________8 Agarose ________________________________________8 1000 g/cm2 ND Sulfate Gels _____________________________________________9 85 C 0.10 % * measured in 1.5% agarose solution Agarose "Molecular Biology Grade" 100 g 500 g 1 Kg 50 g 100 g Agarose "Small Fragments" EP-0010-01 EP-0010-05 EP-0010-10 EP-0020-05 EP-0020-10 Polyacrylamide _____________________________10 - 11 Storage _______________________________________11 Electrophoresis _____________________________________12 SmartLadder The SmartLadder is a ready-to-use molecular weight marker, specially designed for easy quantification as well as size determination. Gel _____________________________________________12 Band size Buffer ___________________________________________12 Sample Loading __________________________________13 Accessories ________________________________________14 Consumables ______________________________________15 ng/band 10000 100 8000 80 6000 60 5000 50 4000 40 3000 30 2500 25 2000 20 1500 15 1000 100 800 80 600 60 400 40 200 20 Band size ng/band 1000 800 SmartLadder SF 2 80 700 600 60 500 400 40 300 200 20 100 SmartLadder SF SmartLadder SmartLadder 100 400 lanes 1000 lanes 200 lanes MW-1700-04 MW-1700-10 MW-1800-02 15 Accessories i-Mupid The Maxi-Plate allows you to cast fullsize gels, and to take advantage of the complete capacity of the i-Mupid. With these 10 x 11cm gels and the two combs that are delivered with it, you can run up to 48 samples at the same time. The Maxi-Plate allows agarose gels only. Size: 10x11 cm Delivered with 2 double combs Maxi-Plate for Mupid-2, -21 and i-Mupid MU-0000-MP The Smart-Comb set consists of two combs which fit into either the regular gel maker or into the Maxi-Plate (see above). These combs allow you to make slots of four different sizes. Smart-Comb set for Mupid2, -21 and i-Mupid MU-0000-SC 14 The Mupid is an ultra-compact electrophoresis system, which breaks with existing trends. It has drawn widespread attention for its convenience and ease of use, and has been used successfully by researchers wordwide. The well-known Mupid-21 has been redesigned and upgraded to the i-Mupid, which now allows the researcher to perform agarose and polyacrylamide gel electrophoresis using a substantially improved power supply. The i-Mupid is a novel and useful device for use in molecular biology and diagnostic labs. User responses have been universally favorable. DANGER! HIGH VOLTAGE! • The i-Mupid should always be operated with caution. Careless handling may result in electrical shock. Never operate damaged or leaking equipment. • Always turn off and remove the power supply before removing the cover. • Certain reagents mentioned in this manual are of a hazardous nature (e.g. ethidium bromide, acetic acid and boric acid). The researcher is cautioned to exercise care with these reagents and with the equipment (e.g. ultraviolet (UV) lamps, electrophoresis apparatus and high-voltage power supplies) mentioned in this manual. Always follow the manufacturer’s safety recommendations. • Never open the voltage transformer or the power supply. If pieces or cables are broken or damaged, never replace them yourself. • Never handle the electrical units with wet hands. • Always keep high-voltage equipment away from heat and liquids. 3 i Sample Loading Gel maker set (ref. MU-000S) Comb Cover for PAGE This set is capable of producing 6 gels (2 large and 4 small) at once. It may also be used for gel storage. Gel Maker Plate (Small) Specifications: Gel Maker Plate (Large) Dimensions: 240 x 28 x 126 mm (WxHxL) Maximum output: 2 large and 4 small gels Gently load the the sample into the well using a micro pipette or micro syringe. l Adding small volumes of glycerol or sucrose to the sample facilitates sample. l The maximum loading volume of sample is about 10 l for a 4 mm thick gel. l Gel fragments can be easily washed out of the well with a micro pipette, syringe or Pasteur pipette. Note: Note : The cover plate is meant for PAGE gels and should not be used for agarose gels. Gel Maker Stand Do not put your fingers in the solution during the electrophoresis run. Power supply Low-cost, compact and lightweight. These features have been achieved by simplifying the circuitry. Easy to operate. Either 35, 50, 100 or 135 V DC can be selected as the output voltage. These voltages are sufficient for ordinary electrophoresis. Place the cover as shown. Reliable. The simplified circuitry ensures a long period of trouble-free, stable operation. This power supply works on pulsating DC current (Pat. pending). This allows resolutions comparable to that run by smooth DC current. In general, a poor separation is due to uneven local gradient potentials, caused by an uneven gel. Dimensions: 44 x 52 x 1115 mm (W x H x L) Input: 100-240 V AC, 50-60 Hz Output: 35, 50, 100 or 135 V DC Fuse: Automatic return type 4 13 Electrophoresis Gel Mini-gel migration tank (not available separately) 1. Holding the vertical portions of the plate, remove the plate containing the gel from the stand. If it is difficult to remove the gel maker plate (for example, if gel is trapped under the base plate), gently push the vertical portions inward. Ease of operation through the directly coupled power supply. Main Unit Cover Both nucleic acids and proteins can be analyzed. Migration distance index line Gels prepared with the gel maker set can be set together with the gel maker plate. Lines with 5 mm spacing are drawn on the gel maker plate, so that the approximate migration distance can be determined at a glance. Gel Marker plate (large) Water level reference For safety reasons, the power supply can not be inserted unless the lid covers the migration tank. 2. Place the gel maker plate on the gel bed in the center of the migration tank. The migration tank accommodates one large or two small plates. Specifications: Migration tank Dimensions: 199 x 75 x 137 mm (W x H x L) Gel size: one large gel measuring 107 x 60 mm (W x L) or two small gels measuring 52 x 60 mm (W x L) can be cast. The electrical circuit is closed by the main unit cover. Buffer 1. Pour buffer in the migration tank to a level slightly (3 to 5 mm) above the gel surface. NOTE: If the cover is clouded, you can clear it by applying a few drops of UF-I on the underside of the lid and wiping the solution evenly over the surface. Re-apply whenever necessary. i-MUPID Electrophoresis system l l MU-0030 The buffer level should be below the reference mark on the migration tank. lf the gel maker plate is completely submerged, the migration pattern will be affected. The buffer level reference mark may also be used for verifying that the migration tank is level. 12 5 Set-up 1- Unpack and carefully examine the power supply, the electrophoresis chamber and the gel maker. 6. After the gel has set, pour a little buffer solution around the comb and slowly draw out the comb. Do not remove the plate for PAGE. The plate should remain attached to the gel. 2- Report any damage to Eurogentec and save all packing material if any part is found to be damaged during transport. 3- Do not attempt to use this apparatus if it is damaged. 4- This apparatus has been designed to be connected with an electrophoresis power supply. l 5- Do not attempt to use the apparatus in any of the following cases: l • Buffer leaks from the main chamber. • The electrophoresis chamber or the safety cover are cracked. • Any of the electrical cables are worn or frayed. l The degree of gel hardening can be judged from the state of acrylamide between the comb teeth. The time required for polymerization varies with the volume and temperature of the gel solution. The polymerization time is normally 30 to 60 minutes, although longer times (2 to 3 hours at 25 C) are ideal. Caution: 6- Place the apparatus close to its electrophoresis power supply. Make sure that this is a safe and dry location. 7- Please refer to the instruction summary for details on how to set up the i-Mupid. Allow the gel to solidify completely. If the gel has not yet completely set or if the comb is withdrawn (too) rapidly, wells may be damaged and/or gel fragments may drop into the well. The resulting bands will be distorted. 8- Warranty 1 year (replacement fuse excluded). Note: • It is important to keep the gel unit clean, particularly the gel maker plate, cover and comb. We recommend that the gel maker set be cleaned with a sponge moistened with detergent, washed in water, and then allowed to dry. • Do not clean any part of the gel unit with organic solvents such as ethanol or acetone. The unit will be damaged by organic solvents and any guarantees will be void. Gel storage If you wish to store gels you have prepared, • Be sure to cover the gel with buffer. • Store the gel at a low temperature • Avoid prolonged storage. 6 11 Instructions for use i Polyacrylamide gel preparation Set the i-Mupid 1. Place the gel maker stand horizontally on the bench. 2. Place the gel maker plate on the gel maker stand. Good results have been obtained by covering the iside of the gel maker plate with a gel bonding sheet. Cut the sheet to the specified size (106 58 mm for a large gel, 51 58 mm for a small gel). These sheets protect the polyacrylamide gel and facilitate handling. 3. Gently pour the de-gassed acrylamide/SDS acrylamide solution between the gel maker plates using a pipette. l The cover included with the system will produce 3 mm-thick gels. About 24 ml of acrylamide is needed for the large gel maker plate and about 12 ml for the small gel maker plate. l If air is trapped between the gel maker stand and the plate, the plate may tilt. To dislodge the air bubble, push the gel maker plate using a pipette or press clown on the vertical portion of the plate. Ensure that no air clings to the gel surface. 4. Place the bottom end of the plate for PAGE in the acrylamide solution in the gel maker plate (see figure). If air bubbles are trapped under the cover, raise the other end and then lower it again to dislodge air bubbles. l Acrylamide can be added through the cover slit for the comb after the gel bond sheet and plate for PAGE are positioned on the gel maker plate. To do this, slowly pipette the acrylamide solution, while moving the pipette from one end of the slit to the other. It is recommended that after the cover is set over the acrylamide solution, acrylamide be added to slightly above the cover slit (as shown below). You only want to set the voltage • Press power on • Set with the “voltage” selector the desired voltage (35, 50, 100 or 135Volts). A green led shows you the selected voltage. • To run the migration, press the “Set” selector (when the power is running a green flickering light can be seen) • To stop the run, press the “power off” selector You want to use your i-Mupid with the timer • Press power on • Set with the “voltage” selector the desired voltage (35, 50, 100 or 135Volts). A green led shows you the selected voltage. • To set the running time press the “+” selector. To increase the time use the “+” selector (maximum 99min). To decrease the time use the “-“ selector (minimum 1min).The timer always start at 30min. • To start the migration, press the “Set” selector (when the power is running a green flickering light can be seen) • A timing countdown can be seen At the end of the selected time the migration is automatically stopped and a bell is heard. Fuse The i-Mupid has got an automatic return type fuse. The circuit could be cut in any abnormal condition (eg heating up condition due to a too concentrate buffer). To reset the power supplyer, you have to remove the electric source cord for at least 30 seconds. After that period, the circuit will return to normal condition. You have to change the buffer with a 0.5 X TBE or TAE. 5. Insert the comb through the cover slit. This is easily accomplished by slightly shifting either the comb or the cover. 10 7 Migration buffer and its temperature Some optimum buffer solutions are given below: If the buffer temperature rises above 40 C during electrophoresis, turn off the power and either dilute the running buffer and/or immerse the longer half of the Migration Tank in an ice bath. Alternatively, the i-Mupid can be used in a cold room. Agarose gel preparation - Preparing gels with the gel maker set For DNA Agarose gels: (cf. p.15) Polyacrylamide gels: Tris EDTA 2Na Acetic acid Add distilled water to make 4.8 g 0.74 g 1.14 ml 1 l (pH 8.1) Tris 60.6 g Boric acid 41.5 g EDTA 2Na 37.2 g Add distilled water to make 1 l (pH 8.3) for storage. Dilute the stock solution 1:10 with distilled water before use. For proteins Agarose gels: (cf. p.15) 1. Place the gel maker stand in a horizontal position. 2. Install the gel maker plate on the gel maker stand. (Note: the cover for PAGE is not required.) One of the ends of the gel maker plates is gray. This is the end where the comb will be placed. The gray color will improve the visibility of the slots. 3. Set the comb. 4. Allow the molten agarose (cf. p. 15) to cool to below 70 C before pouring, to prevent warping of the gel maker plate. 5. Pour the gel. For 4 mm thick gels, about 25 ml of agarose (cf. p. 15) is required for the large gel maker plate and 15 ml for the small gel maker plate. The gel thickness can be modified as needed (see below). Tris 6.0 g Glycine 28.8 g Add distilled water to to make 1 l (pH 8.3) for storage. Dilute the stock solution 1:10 with distilled water before use. SDS polyacrylamide gels: Buffer 1: Tris 15.0 g Glycine 72.5 g Add distilled water to make 500 ml (pH 8.3) for storage. Dilute the stock solution 1:10 with distilled water before use. Buffer 2: NaH2PO4 • 12 H20 35.8 g NaH2PO4 • H20 3.9 g SDS 1.0 g Add distilled water to make 500 ml (pH 7.1) for storage. Dilute the stock solution 1:30 with distilled water before use. 8 (Effective thickness) If air is trapped between the gel maker stand and the plate, the plate may tilt. To dislodge the air bubble, push the gel maker plate using a pipette or press down on the vertical portion of the plate. Ensure that no air clings to the gel surface. 6. After the gel has set, pour buffer solution onto the gel to a level just above the gel surface and gently draw out the comb. Caution: Allow the gel to solidify completely. If the gel has not yet completely set or if the comb is withdrawn (too) rapidly, wells may be damaged and/or gel fragments may drop into the well. The resulting bands will be distorted. 9