Abstract: An apparatus and method for generating an application container are provided. The method includes selecting a target application from among a plurality of applications included in an electronic device, acquiring a policy file corresponding to the target application, determining whether the policy file includes a category of the target application, and executing the application container which includes the target application.

Abstract: An apparatus and method for generating an application container are provided. The method includes selecting a target application from among a plurality of applications included in an electronic device, acquiring a policy file corresponding to the target application, determining whether the policy file includes a category of the target application, and executing the application container which includes the target application.

Abstract: The present invention provides methods for selectively amplifying a mutant allele of a gene. These methods include (a) contacting a sample containing a mutant and a normal allele of a gene with at least one primer that selectively modifies the normal allele of the gene and causes further amplification of the normal allele to fail or to be substantially reduced; and (b) selectively amplifying the mutant allele of the gene or a portion thereof. Other methods for detecting a mutant allele of a gene in a sample are also provided.

Abstract: The invention relates to a method polymerase chain reaction (PCR) and the application thereof A method of PCR performed at ultra-low denaturing temperatures is provided. The denaturing temperatures of the templates adopted are 93-98° C. in the primary 2-3 cycles, and 60-87° C. in the follow-up cycles, those are much lower than 94-96° C., the conventional denaturing temperatures. It is found in the experiment that this method could not only become a universally applied PCR, but also control the reaction specificity by the template selection at ultra-low temperatures. The method possesses unique functions in excluding non-specific amplified products and false-negative results, excluding false-positivity brought about by the contaminants in products and discriminating genomic DNA from cDNA.