Hoefer TE 22 User Manual Download Page 18

 p10

Final assembly and transfer

1

Install the lid

The cassettes are color coded to match the leads in 
the lid. To transfer toward the anode, orient the lid so 
that the grey half of the cassette faces the anode (+), 
or red lead, and the black half of the cassette faces 
the cathode (–), or black lead. Make sure the banana 
plugs seat into the connectors in the lid.

2

Use only an approved power supply such as the 
Hoefer PS 2A200. Make sure the power supply is off 
and all controls are set to zero. Plug the color-coded 
leads from the lid of the transfer unit into the power 
supply — the red lead into the red output jack, and 
the black lead into the black output jack. In most 
systems, the red lead is the anode (+), and the black 
lead is the cathode (–).

3

Cooling is strongly recommended

Any setting that results in higher than 5 W of power 
will generate enough heat to require active heat 
control. A refrigerated circulator bath using water 
should be set to about 10 °C. (If using 50/50 ethyl-
ene glycol/water, the temperature can be set lower.) 
Chill the buffer before use if possible.

 Note: 

Take care in orienting the 

lid so that all species migrate 

toward the membrane when the 

electric field is applied. The 

migration direction depends on 

both the characteristics of the 

sample and the pH of the transfer 

buffer. If the species of interest is 

negatively charged in the transfer 

buffer and the stack is assembled 

so that the membrane is nearest 

the grey side of the cassette, then 

this side faces the anode (+). Most 

proteins migrate toward the anode 

in the Towbin Tris/glycine/metha-

nol buffer system (independent of 

the presence of SDS), and under 

most conditions, nucleic acids 

are negatively charged and also 

migrate toward the anode.

Important! 

Never allow the buffer 

temperature to exceed 45 °C. 

Excessive heat will cause the unit 

to warp.

Typical transfer parameters

Parameters for your sample and buffer system 
must be determined empirically.

 

protein 

nucleic acids

Buffer 

Towbin 

1X TBE or 1X TAE

Current (A) 

0.4 

0.3

Voltage (V) 

~100 

50

Transfer time 

~1 hour 

~1 hour

Coolant temp. 

10 °C 

10 °C or less

Summary of Contents for TE 22

Page 1: ...user manual TE 22 um TE22 IM Rev E0 08 04 Hoefer TE 22 tank transfer unit...

Page 2: ......

Page 3: ...ophoresis Unit function and description 1 Specifications 2 Important information 4 Operating instructions 6 Care and maintenance 12 Troubleshooting 13 Electrotransfer notes 15 Bibliography and referen...

Page 4: ...Inc 953 Indiana Street San Francisco CA 94107 USA support hoeferinc com Hoefer Inc reserves the right to make changes in the specifi cations without prior notice Warranty and liability Hoefer Inc guar...

Page 5: ...rve le droit d effectuer des modifications de ces sp cifications sans aucun pr avis Garantie et responsabilit Hoefer Inc garantit l utilisateur que le produit livr a subi avec succ s tous les essais p...

Page 6: ...sco CA 94107 USA support hoeferinc com Hoefer Inc beh lt sich das Recht vor die Spezifikationen ohne vorhergehende Ank ndigung zu ndern Gew hrleistung and haftung Hoefer Inc garantiert da das geliefer...

Page 7: ...ferinc com Hoefer Inc se reserva el derecho a modificar las especifica ciones sin previo aviso Garant a y responsabilidad Hoefer Inc garantiza que el producto entregado ha sido probado a fondo para co...

Page 8: ...3 Indiana Street San Francisco CA 94107 USA support hoeferinc com Hoefer Inc si riserva il diritto di apportare modifiche ai dati tecnici senza preavviso Garanzia e responsabilit Hoefer Inc garantisce...

Page 9: ...er temperature can be controlled by circulating cooled liquid through the heat exchanger in the base The buffer is separated from the coolant by a heat conducting alumina plate Unpacking Unwrap all pa...

Page 10: ...to 80 Altitude up to 2000 m Installation category II Pollution degree 2 Dimensions w h d 14 24 16 5 cm 5 5 9 5 6 5 in Product certifications EN61010 1 UL3101 1 CSA C22 2 1010 1 CE This declaration of...

Page 11: ...electrode panels 2 electrode retaining screw 2 transfer tank up to four cassettes fit into the slots heat exchanger ports 2 heat exchanger pressure safety valve cassette hook color coded leads fill le...

Page 12: ...ater tap or any coolant source where the water pressure is unregulated For longer runs you can control heating somewhat by chill ing the buffer before use running the unit in a cold room or both When...

Page 13: ...lation d eau un robinet ou quelque source de refroidisse ment dont la pression n est pas r guli re Pour des coulages plus long on peut aussi contr ler la temp rature en refroidissant le tampon avant...

Page 14: ...above atmospheric pressure Set the temperature to 10 C or higher if circulat ing only water If using 50 50 ethylene glycol water the temperature can be set lower Start the circulator bath at the same...

Page 15: ...water Pre wet PVDF or other hydrophobic membranes in methanol Then soak all membrane types in transfer buffer for 2 5 minutes 2 Open the cassette by releasing both latch tabs along the edge opposite t...

Page 16: ...f the stack seems tight replace the top sponge over the gel with a sheet of blotting paper If you remove the bottom sponge below the gel substitute at least two sheets of blotting paper to create spac...

Page 17: ...the sponges Place the tray holding the cassette s near the tank lift out one cassette at a time and slide it into a set of vertical slots Do not discard the buffer 2 Once in place tap the cassette lig...

Page 18: ...et to about 10 C If using 50 50 ethyl ene glycol water the temperature can be set lower Chill the buffer before use if possible Note Take care in orienting the lid so that all species migrate toward t...

Page 19: ...supply Disconnect the leads from the power supply jacks 2 Lift off the lid Use the plastic hook stored in the holder at the side of the unit to lift up a cassette just far enough to be able to grab i...

Page 20: ...llow the unit to air dry completely Periodically wash with a dilute solution of a mild detergent Removing the electrode panel s For more thorough cleaning or to replace damaged electrodes remove each...

Page 21: ...bly instructions on page 7 Grid pattern on membrane Add extra sheets of blotting paper to increase the clearance between the cassette panel and the gel Take care not to overstuff the cassette the gel...

Page 22: ...eters Fix or crosslink the molecule onto the membrane according to the requirements of the nucleic acid protein or membrane type Prepare protein transfer buffer without SDS Verify the optimal amount o...

Page 23: ...s to a membrane increases the sensitivity of detection methods such as autoradiography and permits detection of specific proteins by antibodies or affinity labels and of specific nucleic acids by hybr...

Page 24: ...s such as pH salt type and concentration and the presence of detergents such as sodium dodecyl sulfate SDS Condi tions required for efficient elution may not coincide with optimal conditions for bindi...

Page 25: ...circulator bath set to 10 C if using water as a coolant You can use a lower setting if the coolant is 50 50 ethylene glycol water Never leave the unit unattended for more than one hour under high powe...

Page 26: ...ol from the transfer buffer Gershoni and Palade obtained a much more quantitative transfer The disadvantage of cationic membrane is that protein stains also bind well so that the stain ing background...

Page 27: ...ne FW 75 07 192 mM 28 8 g SDSa FW 288 4 0 1 3 5 mM 2 0 g Dissolve in 1 5 liters distilled water Add methanol as requiredb Bring to 2 liters with distilled water Do not adjust the pH which should be be...

Page 28: ...ash gels three times 20 minutes each to assure complete removal of denaturants and detergents See Bittner et al for a study of the transfer effi ciency for DNA of different sizes The Bittner transfer...

Page 29: ...down to 0 1X may be used should it be necessary to decrease the amount of current in the system in order to control overheating RNA transfer buffer 10X 10X Tris acetate EDTA TAE b pH 8 4 1 liter Tris...

Page 30: ...ed nitrocellulose and radiographic detection with antibody and radioiodinated protein A Anal Biochem 112 195 1981 Gallagher S Winston S E Fuller S A and Hurrell J G R Immunoblotting and Immunodetectio...

Page 31: ...Sci USA 76 3116 1979 Sambrook J and Russell D W Molecular Cloning A Laboratory Manual Cold Spring Harbor Labora tory Press A1 17 2001 Southern E M Detection of specific sequences among DNA fragments s...

Page 32: ...d 1 TE24 1 foam sponge 6 mm thick Foam sponges 9 10 5 cm 6 mm thick 4 TE25 Foam sponges 9 10 5 cm 3 mm thick 4 TE25F 1 8 Electrode panel 1 TE23 Safety lid with cables 1 TE29 High voltage leads with ja...

Page 33: ......

Page 34: ...p27 Printed in the USA Hoefer Inc 953 Indiana Street San Francisco CA 94107 USA www hoeferinc com Contrad 70 and Decon 90 are trademarks of Decon Lab...

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