Western Blot Protocol

For further assistance, please contact our technical service department.

 Problem: No Bands Observed

Possible Source	Suggestion
Insufficient antibody	Antibody may have low affinity to protein of interest. Increase antibody concentration (2-4 fold higher than recommended starting concentration).
	Antibody may have lost activity. Perform a Dot Blot.
Insufficient protein	Increase the amount of total protein loaded on gel.
	Confirm the presence of protein by another method.
	Use a positive control (recombinant protein, cell line or treat cells to express analyte of interest).
	Perform a Dot Blot.
Poor transfer	Wet PVDF/Immobilon-P membrane in methanol or nitrocellulose membrane in transfer buffer.
	Ensure that there is good contact between PVDF membrane and gel.
Incomplete transfer	Optimize transfer time. High MW protein may require more time for transfer.
	To ensure transfer is complete, stain the membrane with Ponceau S, Amido Black or India Ink.
	Use prestained MW marker.
Over transfer	Reduce voltage or time of transfer for low molecular weight proteins (< 10 kDa).
Isoelectric point is >9	Use alternative buffer system with higher pH such as CAPS (pH 10.5).
Incorrect secondary antibody used	Confirm host species and Ig type of primary antibody.
Old antibody	If antibody is expired or past manufacturer warranty, purchase fresh antibody.
Incorrect storage of antibodies	Follow manufacturer's recommended storage and avoid freeze/thaw cycles.
Sodium Azide contamination	Make sure buffers do not contain Sodium Azide as this can quench HRP signal.
Insufficient incubation time with primary antibody	Extend incubation time to overnight at 4°C.

 

 

 

Problem: Faint Bands (Weak Signal)

Possible Source	Suggestion
Low protein-antibody binding	Reduce the number of washes to minimum.
	Reduce NaCl concentration in Blotting Buffer used for wash steps (recommended range 0.15M - 0.5M).
	Reduce NaCl concentration in Antibody Solution (recommended range 0.15M - 0.5M).
Insufficient antibody	Antibody may have low affinity to protein of interest. Increase antibody concentration (2-4 fold higher than recommended starting concentration).
Insufficient protein	Increase the amount of total protein loaded on gel.
Inactive conjugate	Mix enzyme and substrate in a tube. If color does not develop or, it is weak. Make fresh or purchase new reagents. Switch to ECL.
Weak/Old ECL	Purchase new ECL reagents.
Non-fat dry milk may mask some antigen	Decrease milk percentage in Block and Antibody Solutions or substitute with 3% BSA.

 

 

 

Problem: Extra Bands

Possible Source	Suggestion
Non-specific binding of primary antibody	Reduce primary antibody concentration.
	Reduce the amount of total protein loaded on gel.
	Use monospecific or antigen affinity purified antibodies.
Non-specific binding of secondary antibody	Run a control with the secondary antibody alone (omit primary antibody). If bands develop choose an alternative Secondary Antibody.
	Use monospecific or antigen affinity purified antibodies.
Non-specific binding of primary or secondary antibodies	Add 0.1 - 0.5% Tween20 to primary or secondary Antibody Solution.
	Use 2% non-fat dry milk in Blotting Buffer as a starting point to dilute primary and secondary antibodies. Adjust antibody concentration up or down as needed.
	Increase number of washes.
	Increase NaCl concentration in Blotting Buffer used for antibody dilution and wash steps (recommended range 0.15M - 0.5M).
	Increase Tween20 concentration in Blotting Buffer used for wash steps (0.1%-0.5%).
Aggregation of analyte	Increase amount of DTT to ensure complete reducing of disulfide bonds (20 -100mM DTT). Heat in boiling water bath 5-10 minutes before loading onto gel.
	Perform a brief centrifugation.
Degradation of Analyte	Minimize freeze/thaw cycles of sample.
	Add protease inhibitors to sample before storage.
	Make fresh samples.
Contamination of reagents	Check buffers for particulate or bacterial contamination. Make fresh reagents.

 

 

 

Problem: High Background

Possible Source	Suggestion
Non-specific binding of primary antibody	Use monospecific or antigen affinity-purified antibodies.
	Block in 5% milk. Adjust the milk (2-5%) or NaCl (0.15-0.5M) concentrations of primary Antibody Solution.
	Decrease antibody concentration.
Non-specific binding of secondary antibody	Run a control with the secondary antibody alone (omit primary antibody). If bands develop choose an alternative Secondary Antibody.
Insufficient blocking	Start with 5% dry milk with 0.1%- 0.5% Tween 20, 0.15 -0.5M NaCl in 25mM Tris (pH 7.4). Incubation time may be extended. Adjust milk concentration up or down as needed.
	Overnight blocking at 4°C may decrease blocking efficiency since detergents might not be effective at lower temperatures.
Non-fat dry milk may contain target antigen	Substitute with 3% BSA.
Non-fat dry milk contains endogenous biotin and is incompatible with avidin/streptavidin	Substitute with 3% BSA.
Some IgY antibodies may recognize milk protein	Substitute with 3% BSA.
Insufficient wash	Increase number of washes.
	Increase Tween 20 concentration in Wash Buffer (0.1%-0.5%).
Non-Specific Binding of Primary Antibody	Increase NaCl concentration in primary Antibody Solution and Blotting Buffer used for dilution of primary antibody and wash steps (recommended range 0.15M - 0.5M).
Film overexposed	Reduce exposure time.
	If target signal is too strong wait 5-10 minutes and re-expose to film.

 

 

 

Problem: Diffuse Bands

Possible Source	Suggestion
Excessive protein on gel	Reduce amount of protein loaded

 

 

 

Problem: White Bands (ECL method)

Possible Source	Suggestion
Excessive signal generated	Reduce antibody or protein concentration. Excessive antibody or protein can cause extremely high levels of localized signal (usually at a single band). This results in rapid, complete consumption of substrate at this point. Since there is no light production after the completion of this reaction, white bands are the result when exposed to film.

 

 

 

Problem: Patchy uneven spots all over the blot

Possible Source	Suggestion
Contamination of reagents	Check buffers for particulate or bacterial contaminate. Make fresh reagents.
Not enough solution during incubation or washing	Make sure membrane is fully immersed during washes and antibody incubations.
Air bubble trapped in membrane	Gently remove any air bubbles. Especially during transfer.
Uneven agitation during incubations	Ensure uniform agitation by placing on a rocker/shaker.
Contaminated equipment	Make sure that the electrophoresis unit is properly washed. Protein or pieces of gel remaining on the unit may stick to the membrane. Wash membrane thoroughly.
HRP aggregation	Filter conjugate to remove HRP aggregates.
Long exposure	Reduce exposure time.