Streptavidin-plus® (Streptomyces avidinii) is specifically manufactured for coated plate and other immobilization applications, or where higher temperature stability is required.
Supplied lyophilized, contains ~0.9 mg protein/mg lyophilizate
Specific activity: >14.0 U/mg protein
Size: Available in 10 mg and 100 mg pack sizes.
Product Code: SA20
Q. Can I use water to dissolve the material, or do I have to use PBS?
A. Streptavidin is readily soluble in water or salt-containing buffers, up to 50 mg/ml or more.
There is a tendency for lyophilized streptavidin to aggregate when it is re-dissolved in water or other low ionic strength buffers at neutral or acidic pH. ProZyme Streptavidin has been lyophilized from a dilute sodium chloride solution at mildly alkaline pH in order to minimize aggregate formation. In rare cases Streptavidin may contain a small amount of insoluble material when dissolved in de-ionized water or low ionic strength buffers, either at the time it is dissolved or after freezing and re-thawing. This effect is generally not seen in the presence of salt-containing buffers such as PBS. If undissolved material is observed, it can be removed by centrifugation and does not constitute a significant fraction of the total protein.
Our SA20 Technical Data Sheet contains further information.
Q. How do I reconstitute the streptavdin to avoid aggregate formation?
Our standard technique for a 1 gram or 100 mg bottle is to add enough buffer to dissolve to 20 – 50 mg/ml, and immediately begin swirling the bottle (for instance holding it on a counter-top and moving the bottle fairly rapidly in a tight circular motion). We keep this up until we see the protein has dissolved, which might take a couple of minutes. This minimizes aggregate formation, but there is often a little cloudiness that should be removed by centrifugation prior to using the material. When dissolved this way, the recovery after centrifugation should be as stated on the bottle when measured by A280.
This is most important when re-dissolving in water or low ionic strength buffers (as mentioned in the SA20 Tech Data Sheet); dissolving in PBS and higher ionic strength buffers seems to be less sensitive to constant agitation. But even when using PBS, one should not just add the buffer and leave the bottle sitting undisturbed on the bench while waiting for the streptavidin to dissolve.
For 10 mg samples and other samples dispensed to microcentrifuge tubes, the usual procedure is to add enough buffer to dissolve to 5 – 50 mg/ml, and mix by up and down pipetting until the contents appear to have dissolved. With these small samples, re-dissolving is rapid.
Product Safety Documentation for SA20:
from $ 350.00
from $ 350.00