摘要:
Described herein are embodiments of USB device control using endpoint type detection during enumeration. An apparatus configured for USB device control using endpoint type detection during enumeration may include a host controller configured to selectively disable enumeration of a USB device based at least in part on an endpoint type of the USB device. The apparatus may include a management engine configured to store in the host controller a USB lock policy defining endpoint types disallowed to be enumerated by the apparatus. Other embodiments may be described and/or claimed.
摘要:
Described herein are embodiments of USB device control using endpoint type detection during enumeration. An apparatus configured for USB device control using endpoint type detection during enumeration may include a host controller configured to selectively disable enumeration of a USB device based at least in part on an endpoint type of the USB device. The apparatus may include a management engine configured to store in the host controller a USB lock policy defining endpoint types disallowed to be enumerated by the apparatus. Other embodiments may be described and/or claimed.
摘要:
In one embodiment, a flash sharing controller is to enable a plurality of components of a platform to share a flash memory. The flash sharing controller may include: a flash sharing class layer including a configuration controller to configure the plurality of components to be flash master devices and configure a flash sharing slave device for the flash memory; and a physical layer coupled to the flash sharing class layer to communicate with the plurality of components via a bus. Other embodiments are described and claimed.
摘要:
Compositions, methods and a kit are described relating to a novel family of enzymes which preferentially bind to a hydroxymethylated cytosine or a glucosylated hydroxymethylated cytosine and cleave double-stranded DNA at a defined distance 3′ of the recognition site to produce a cleavage fragment with a 1-3 base overhang.
摘要:
Methods are provided for making restriction endonucleases with reduced star activity by one or more targeted mutations to a catalytic site within the restriction endonuclease. Examples of modifications to restriction endonucleases with significant sequence identity with KpnI are provided and reduced star activity demonstrated.
摘要:
A restriction endonuclease is provided that has been engineered to have a cleavage specificity for a DNA recognition sequence containing a modified nucleotide. Methods for engineering enzymes to cleave DNA containing modified nucleotides at specific sequences are provided.
摘要:
Recombinant nicking endonucleases and associated methylases have been obtained and sequenced and their specificity has been defined. A mutant form of the nicking endonuclease has been cloned where the mutation includes deletion of amino acid sequences at the C-terminal end of the protein. The nicking enzymes have been used for a number of purposes including: amplifying DNA from as few cells as can be found in a single bacterial colony in the presence of a strand displacing polymerase; and for removing genomic DNA in a biological preparation where it is deemed to be a contaminant.
摘要:
A nicking endonuclease is described which has an amino acid sequence with at least 70% identity to SEQ ID NO:6 and comprising a mutation at least one of an arginine or gutamic acid corresponding to position 507 and position 546 respectively in SEQ ID NO:6.
摘要翻译:描述了一种切口内切核酸酶,其具有与SEQ ID NO:6具有至少70%同一性的氨基酸序列,并且包含分别对应于SEQ ID NO:6中的位置507和位置546的精氨酸或谷氨酸中的至少一种的突变 。
摘要:
Compositions, methods and a kit are described relating to a novel family of enzymes which preferentially bind to a hydroxymethylated cytosine or a glucosylated hydroxymethylated cytosine and cleave double-stranded DNA at a defined distance 3′ of the recognition site to produce a cleavage fragment with a 1-3 base overhang.
摘要:
The present invention relates to recombinant DNA which encodes the BsaI restriction endonuclease as well as BsaI methylase, expression of BsaI restriction endonuclease and BsaI methylase in E. coli cells containing the recombinant DNA, and purification of BsaI restriction endonuclease to near homogeneity.