Micromilli - 生物技术资讯

 cystal of ice will form that can mechanically shear the protein.the same as DNA.
for storage of DNA, it is better to be stored in buffer to avoid such mechanical shearing and hydrolysis, if you concern about EDTA, you can use Tris-HCl (pH 8.0).
    Here is some general guide for storage of purified proteins:
    For short term storage (up to 24 h), most proteins can be kept at 4C.
    For storage times longer than 24 h r at 4C, it may be necessary to filter sterilize the protein preparation (through a 0.22um filter) or to add a bacteriostatic agent (e.g. 0.1% sodium azide) to avoid bacterial growth. Note that not all proteins are stable at 4C for longer periods.
    For long term storage (more than a week), it becomes necessary to freeze the protein preparation. It is important to freeze it rapidly using liquid nitrogen or a dry ice/ethanol mixture to avoid denaturation. It is also important to freeze the solution in small aliquots to avoid repeated freezing and thawing which may reduce the biological activity or affect the structure (e.g., antibodies, enzymes). Several stabilizing agents can be added, such as glycerol (5-50% (w/v)), serum albumin (10 mg/ml), reducing agents (such as 1 mM DTT), and ligands (the nature and concentration depending on the nature and concentration of the target protein).
    If you want to store your protein preparation for several months, you can store it at -20C. At this temperature it is necessary to add 50% glycerol to the solution to avoid freezing. The sample can be prepared in two ways: Add an equal volume of pure glycerol to the protein preparation. Or dialyze the protein preparation against the storage buffer containing 50% glycerol. This method has the additional advantage
that it results in an approx. threefold concentration.
    If you need to store your protein preparation for longer periods (months to years), you should freeze it at -70C or even in liquid nitrogen. Although it is not really necessary to add glycerol at these temperatures, the addition of 5-50% glycerol could help to keep the protein stable.
    Alternative methods are:
    Storage of the protein at 4C as an ammonium sulfate precipitate.
    Storage of the protein at 4C or lower in a lyophilized form.
    For the lyophilization it is necessary that the protein is dissolved in a volatile buffer (such as trimethylamine/HCl;pH range 6.8-8.8). Note that not all proteins are stable during the freeze-drying process. one more thing i should mention in supplement to this guide, trace of protease will definitely degrade the protein, though addition of protease inhibitors seems fine, it is suggested a further purification is needed.
From: Mitbbs_Biology

转自：http://blog.bioon.com/user3/23402/archives/2009/231294.shtml