ZOOM™ IPGRunner™ Combo Kit

There are several reasons why streaking may occur.

(1) Sample is not completely solubilized prior to application.

(2) Sample is poorly soluble in rehydration solution.

(3) Non-protein impurities in the sample can interfere with IEF, causing horizontal streaking in the final 2-D result, particularly toward the acidic side of the gel.

(4) Ionic impurities are present in sample.

(5) Ionic detergent is present in sample.

(6) Sample load is too high.

(7) Underfocusing. Focusing time was not long enough to achieve steady state focusing.

(8) Overfocusing. Extended focusing times (over 100,000 Vh) may result in electroendosmotic water and protein movement, which can produce horizontal smearing.

What should be done?

(1) Be sure that the sample is completely and stably solubilized. Note: Repeated precipitation-resolubilization cycles produce or increase horizontal streaking.

(2) Increase the concentration of the solubilizing components in the rehydration solution.

(3) Modify sample preparation to limit these contaminants or dialyze protein.

(4) Reduce salt concentration to below 10 mM by dilution or desalt the sample by dialysis. Precipitation with TCA and acetone and subsequent resuspension is another effective desalting technique that removes lipids, nucleotides and other small molecules.
Note: Specific and non-specific losses of proteins can occur with dialysis, gel chromatography, and precipitation/resuspension of samples. If the sample preparation cannot be modified, the effect of ionic impurities can be reduced by modifying the IEF protocol. Limit the voltage to 100-150 V for 2 hours, then resume a normal voltage step program. This pre-step allows the ions in the sample to move to the ends of the IPG strip.

(5) If the ionic detergent SDS is used in sample preparation, the final concentration must not exceed 0.25% after dilution into the rehydration solution. Additionally, the concentration of the non-ionic detergent present must be at least 8 times higher than the concentration of any ionic detergent to ensure complete removal of SDS from the proteins.

(6) Extend focusing time. Load less sample.

(7) Prolong focusing time.

(8) Reduce focusing time.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

With the ZOOM system, it is not recommended to use a voltage higher than 2000 V. The ZOOM IPG Runner System is rated to 3500 VDC and 3.5 Watts, but for performing IEF, the results are optimal at maximum of 2000 V and 0.1 W per strip (~50 µA per strip).

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

To avoid modification of proteins, never heat a sample over 37 degrees C after adding urea. Elevated temperatures cause urea to hydrolyze to isocyanate, which modifies proteins by carbamylation.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

We do not recommend using more than 0.2% SDS. If the percentage of SDS is too high, all the proteins will be negatively charged and will migrate to the positive electrode.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

A typical load amount is 5-10 µg for silver staining and 10-50 ug for Coomassie staining. We have determined that 400 µg of protein can be focused on our 7 cm strips with a mixture of purified standard proteins. To load this much protein, some cleaning up (like pre-fractionation) of crude lysate is required. Often this is because of the large dynamic range between "high abundance" proteins vs "low abundance" proteins, making the most abundant proteins the load-limiting factor. This is cell/tissue dependent. When testing sample preparation and run parameters, we recommend that the typical load recommended above for the stain of choice be used. After satisfactory results are obtained, higher loads can be run. Longer run times may be required when using higher loads.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.