US2007166751A1PendingUtilityA1

Compositions and Methods for Nucleic Acid Extraction from Biological Samples

60
Assignee: SIGMA ALDRICH COPriority: Dec 17, 2002Filed: Mar 19, 2007Published: Jul 19, 2007
Est. expiryDec 17, 2022(expired)· nominal 20-yr term from priority
C12N 15/1003
60
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Claims

Abstract

Methods and compositions for extracting nucleic acids from a biological sample are provided. The extraction compositions contain a protease enzyme such as proteinase K at alkaline pH with little or no surfactant present. Extraction can be efficiently performed in 60 minutes or less at room temperature for certain mammalian tissue samples and at elevated temperatures for certain plant tissues.

Claims

exact text as granted — not AI-modified
1 . A method for extracting nucleic acids from a tissue sample obtained from a mammal, the method comprising incubating the sample at room temperature in an extraction composition which contains a protease enzyme and a buffer component which buffers the composition to a pH of 7.5 or greater for an incubation time of not more than 30 minutes.  
   
   
       2 . The method in accordance with  claim 1  wherein the extraction composition does not contain a surface active agent.  
   
   
       3 . The method in accordance with  claim 1  wherein the protease enzyme is a subtilisin-like serine protease.  
   
   
       4 . The method in accordance with  claim 3  wherein the subtilisin-like serine protease is proteinase K.  
   
   
       5 . The method in accordance with  claim 4  wherein the proteinase K is present at a concentration of about 50 Units/ml or greater.  
   
   
       6 . The method in accordance with  claim 5  wherein the proteinase K is present at a concentration of about 100 Units/ml or greater.  
   
   
       7 . The method in accordance with  claim 1  wherein the extraction composition comprises not more than about 100 mM EDTA.  
   
   
       8 . The method in accordance with  claim 7 , wherein the extraction composition comprises about 10 mM EDTA.  
   
   
       9 . The method in accordance with  claim 1 , wherein the buffer component is Tris-HCl.  
   
   
       10 . The method in accordance with  claim 9 , wherein the Tris-HCl is present at a concentration of about 80 mM or greater.  
   
   
       11 . The method in accordance with  claim 1  wherein the extraction composition is buffered to a pH of at least 8.0 or greater.  
   
   
       12 . The method in accordance with  claim 1  wherein the incubating is for not more than about 20 minutes.  
   
   
       13 . The method in accordance with  claim 12  wherein the incubating is for not more than about 10 minutes.  
   
   
       14 . The method in accordance with  claim 13  wherein the mammalian tissue sample comprises a mouse tail tissue or a mouse ear tissue.

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