1% SDS is the lysis buffer of choice for most western blots or
the case of the missing protein in western blots.

 As mentioned in my opening blog, good antibodies sometimes do not work because of poor technique. One of the most common problems of this type is the failure to solubilize cellular proteins in the lysis step prior to western blot analysis. Thus, after centrifugation of the cell lysate many cellular proteins are discarded with the pellet and are consequently missing (not detected) from the western blot.  This problem occurs principally because of the use of nonionic detergents such as NP-40 or triton for cell lysis. These detergents fail to solubilize many cellular proteins involved in cell signaling. This problem is particularly acute in brain where synaptic junctions are known to be insoluble in nonionic detergents. To obviate this problem, the lysis buffer of choice for western blots is virtually always 1% SDS which completely solubilizes membrane and other hard to solubilize proteins and even synaptic junction proteins. As an added advantage, SDS also inactivates many cellular proteases. However, inclusion of protease inhibitors with the 1% SDS is often recommended as some proteases are insensitive to or even activated (e.g. proteinase K) by SDS. Some researchers use buffers that contain 0.1% SDS such as the RIPA buffer. While this is an improvement over nonionic detergents, it still leaves some proteins in the synaptic junction unsolubilized. 

Phospho-specific antibodies
The use of nonionic detergents is made even more problematic when the phosphorylation state of a protein is assayed in western blots using phosphospecific antibodies. This is because nonionic detergents are ineffective in blocking protein phosphatase activity. Virtually all cellular lysates contain high levels of phosphatase activity such that the lysate proteins can be completely dephosphorylated in a matter of minutes or even seconds. This would make it impossible for a phosphospecific antibody to work in a western blot as its phosphorylation target has been removed by the phosphatases. Fortunately, the 1% SDS lysis buffer described above has the added benefit that it completely denatures protein kinases and phosphatases.

Exceptions to the rule
1.    Subcellular fractionation and/or protein-protein interaction.
Because 1% SDS disrupts cell organelles, it is obviously NOT recommended if isolation of cellular organelles such as membranes, mitochondria and nuclei is required.  However, once the organelles have been isolated, it is essential that 1% SDS be used to lyse the organelle fraction to insure solubilization of all the proteins in the organelle. Similarly SDS solubilization is NOT recommended when analyzing protein-protein interactions as SDS disrupts these interactions.

2.    Immunoprecipitation.
Antibodies are inactivated by 1% SDS and this makes immunoprecipitation from the SDS lysis buffer difficult. This effect can be overcome in some cases (Goebel-Goody et al. 2009) but in the absence of such procedures immunoprecipitation from 1% SDS is not recommended. Non-ionic detergents do not typically inactivate antibodies and these detergents are commonly used prior to immunoprecipitation. However, it must also be recognized that the lysate prepared by using nonionic detergent is missing a number of key proteins. So immunoprecipitation from such lysates must be interpreted with this factor in mind.

Want to try our lysis buffer for yourself? You can buy it here: 10X Western Lysis Buffer

While choosing the right lysis buffer is critical to western success, none of this matters if the antibody being used is not reproducible.

For detailed steps on lysate preparation, check out our Lysate Preparation Protocol!

Using 1% SDS and still ending up with goop? Check out our blog on The Truth about Goopy Lysate!

More Protocols: We also have in-depth protocols for Western Blotting and Phosphatase Treatments.

Davies, KD, Goebel-Goody, SM, Coultrap, SJ and Browning, MD (2008) Long-term synaptic depression that is associated with GluR1 dephosphorylation but not AMPA receptor internalization. J Biol Chem.283:33138-46.
Goebel-Goody, SM, Davies, KD, Linger, RA, Freund,R and Browning, MD. (2009) Phospho-regulation of synaptic and extrasynaptic NMDA receptors in adult hippocampal slices.  Neuroscience 158:1446-1459
1% SDS is the lysis buffer of choice for most western blots
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1% SDS is the lysis buffer of choice for most western blots
Using 1% SDS (an ionic detergent) in the lysis step prior to Western blotting completely solubilizes membranes and other hard to solubilize cellular proteins.
Mike Browning
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6 thoughts on “1% SDS is the Lysis Buffer of Choice for Most Western Blots

  1. When you use non-ionic detergents for lysis, you can include 150 mM NaCl to help retain proteins that would normally be lost without salt with non-ionic detergents. This will give you a better isolation for Co-IP experiments. The buffer I use is: 1% Triton X-100, 50 mM Tris pH 8.0, 150 mM NaCl + 1x protease inhibitors + 5 mM EDTA.

    An added benefit of using this buffer is that it doesn’t lyse the nucleus, thus preventing the lysate from becoming overly viscous from all of the DNA.

    1. You are quite right Darius that non-ionic detergents require NaCL to work effectively. However, remember this buffer will not solublize the synapse and thus in CO-IP the pellet will artifactually contain synaptic proteins. This can be avoided by preclearing the lysate by centrifugation before adding the antibody. Of course then synaptic proteins cannot be accurately studied in CO-IP of such a lysate. Obviously this is primarily a brain problem.

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