Abstract:
Electroporation of mammalian cells is performed to high efficiency by use of a buffer solution containing trehalose, sucrose, or both, in addition to an inorganic phosphate buffer, an organic sulfonic acid buffer, a halide sa lt of an alkali or alkaline earth metal, a chelating agent, an alkyl methyl sulfoxide, and a nucleotide triphosphate, with substantially no sodium. This buffer solution is effective both in the electroporation of cells that are suspended in the buffer solution and in the electroporation of cells that ar e fixed on a surface.
Abstract:
Biological cells and other membranous structures are transfected in a flo w-through system by first rendering the structures magnetically active such that they respond to a magnetic field, suspending the structures in a soluti on of an exogenous species with which the structures are to be transfected, then placing the suspension in a channel and using a moving magnetization pa ttern along the channel wall to cause the structures to travel through the c hannel. Along their path of travel, the structures pass a transmitter that e mits transfection energy sufficient to cause the exogenous species in the su spension to permeate the structure membranes and enter the interiors of the structures.
Abstract:
A chamber that includes electrical contacts and a protective lid with a m anually operated release is designed to receive a multi-well electroporation plate and to allow high-throughput electroporation on the well contents wit h minimal risk of electrical shock to the user and minimal opportunity for s ample loss and contamination.
Abstract:
A chamber that includes electrical contacts and a protective lid with a manually operated release is designed to receive a multi-well electroporation plate and to allow high-throughput electroporation on the well contents with minimal risk of electrical shock to the user and minimal opportunity for sample loss and contamination.
Abstract:
Biological cells and other membranous structures are transfected in a flow-through system by first rendering the structures magnetically active such that they respond to a magnetic field, suspending the structures in a solution of an exogenous species with which the structures are to be transfected, then placing the suspension in a channel and using a moving magnetization pattern along the channel wall to cause the structures to travel through the channel. Along their path of travel, the structures pass a transmitter that emits transfection energy sufficient to cause the exogenous species in the suspension to permeate the structure membranes and enter the interiors of the structures.
Abstract:
The present invention relates in general to microscopy systems. In particular, the present invention relates to microscopes rendering digital images of samples, with the capability to digitally control the focus of the microscope system, and the software used to control the operation of the digital microscope system. Further, the present invention relates to a microscope structure that allows for compact and multi-functional use of a microscope, providing for light shielding and control with samples that require specific light wavelength characteristics, such as fluorescence, for detection and imaging.