Life Technologies Corporation

Invitrogen Corporation

Whatman Gmbh

Robert W Blakesley

Robert W Flesher

Robert William Lynn

Kevin J Barnes

Mindy D Goldsborough

Mark S Berninger

Kevin T Barnes

The invention relates to a solid medium or matrix for storage of nucleic acid molecules (e.g. RNA and/or DNA), particularly vectors and especially plasmids, comprising a solid matrix preferably having a compound or composition which protects against degradation of nucleic acids incorporated into or absorbed on the matrix. The invention also relates to methods for storage or isolation/purification of nucleic acids using this solid medium, and in situ use of the stored or isolated/purified nucleic acids.

Archiving of vectors

Methods for preventing inhibition of nucleic acid synthesis by pyrophosphate are disclosed. More specifically, the present invention concerns inhibiting or preventing pyrophosphorolysis in sequencing and amplification of nucleic acid molecules. According to the present invention, an enzyme which is a pentosyltransferase, a phosphotransferase with an alcohol group as acceptor, a nucleotidyltransferase, or a carboxy-lyase is added to the reaction which serves to remove pyrophosphate from the reaction mixture.

Methods for preventing inhibition of nucleic acid synthesis by pyrophosphate

An apparatus provides for casting a gel and for presenting the gel for electrophoresis. The apparatus comprises a casting tray and the casting plate which combine to form a mold for the gelable liquid, and an electrophoresis tank in which the electrophoresis process occurs. The floor of the electrophoresis tank rises to form the plate pedestal upon which the casting plate rests during electrophoresis. The floor of the electrophoresis tank forms a cavity at the edges of the plate pedestal in which the casting tray rests during the electrophoresis process. The casting plate is first firmly seated in the bottom of the casting tray forming a mold for the gelable liquid. The gelable liquid is poured into the mold. The comb is placed in the comb slots so as to form wells in the gel. The gelable liquid is allowed to gel, and the comb is removed. The material to undergo electrophoresis is placed in the wells left by the comb. The entire assembly is then placed and aligned on the plate pedestal. The casting tray is then pushed down into the casting tray well. Electrophoresis buffer sufficient to fill the tank to approximately the top of the gel is then poured into the electrophoresis tank. An alternate embodiment is shown.

Pop up electrophoresis apparatus and method

Electrophoresis sequencing apparatus

Electrophoresis sequencing apparatus tray

A vertical gel slab electrophoresis apparatus is disclosed comprised of a vertically oriented gel slab arranged between upper and lower buffer solution reservoirs. A bifurcated movable lower tray contains both an upper buffer reservoir drain and lower buffer reservoir. Both upper and lower buffer reservoirs are provided with hinged covers which act as electrical interlocks to prevent unsafe operation of the apparatus, as well as prevent spillage of buffer solution. The design overcomes safety problems associated with both electrical shock and radioactive chemical contamination. The apparatus is provided with handles for each relocation. Cooling vents are provided for ambient air cooling of the apparatus. A gel mold experiment can be assembled and disassembled with unusual ease with the aid of unique self-locking clamp assemblies.

Vertical gel slab electrophoresis apparatus

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Frederick, MD, United States of America

Robert W Blakesley