About Dmitry Kuksin

A Ph.D. graduate from the Department of Microbiology with a concentration in Virology. My studies have focused on Simian Virus 40 (SV40), a polyomavirus, its entry, trafficking, and pathway to infection. The focal point of my research has been the detection and tracking of input SV40 genomes from the endoplasmic reticulum to the host cell nucleus.

Using Image Cytometry for the Detection and Analysis of GFP Expression

Perform image-based GFP analysis WITHOUT all of the set-up, maintenance, and data manipulation required for flow. Measure GFP Expression Efficiency Using Image Cytometry — In just a few clicks, Cellometer Vision CBA generates brightfield and fluorescent cell images, and detailed data reports. Detection of GFP expression to quantify the transfection/transduction efficiency. Single assay for measuring GFP expression and viability Measurement of other fluorescent proteins Detection of GFP Expression to Quantify the Transfection/Transduction Efficiency Quantitative measurement of GFP expression using Cellometer Load only 20 µl sample into counting chamber Capture and analyze brightfield and fluorescent cell images automatically Data [...]

By |2021-06-15T20:44:43+00:00June 25th, 2013|Categories: Cell Counting Leadership, Cellometer Application News|0 Comments

Measure GFP Expression Efficiency Using Image Cytometry

What is GFP? Green Fluorescent Protein (GFP) is a 26.9 kDa protein first identified in crystal jellyfish, Aequorea victoria. It was discovered that when exposed to blue or ultraviolet light the protein fluoresces green. After GFP was first expressed in E. coli in 1994 it was soon confirmed that GFP can also be successfully expressed in other organisms as well. Since then, not only have many fluorescent proteins of different colors been generated, but their function is enhanced to provide a faster and stronger fluorescent signal. GFP Applications GFP is often used as a reporter of gene or protein expression. [...]

By |2021-06-15T20:44:59+00:00May 29th, 2013|Categories: About Cell-Based Assays, Cell Counting Leadership|0 Comments

Fluorescence-Based Cell Cycle Analysis – Drug Study – Part 2

Jurkat cells were used to analyze cell cycle kinetics following treatment with the cell-cycle-arresting drug etoposide.  Etoposide is designed to arrest the cells at the G2 phase of the cell cycle. Jurkat cells were incubated with media only (control) or etoposide (0.06 µM, 0.12 µM) for 24 hours. Control and drug-treated cells were ethanol fixed and stained with cell cycle propidium iodide reagent. For each sample, 20 µl of cell sample (at ~4 x 106 cells / mL) was loaded into a Cellometer imaging chamber, inserted into the Vision CBA Analysis System, and imaged in both bright field and fluorescence. [...]

By |2021-06-15T20:45:09+00:00May 13th, 2013|Categories: About Cell-Based Assays, Cell Counting Leadership|0 Comments

Fluorescence-based Cell Cycle Analysis-Part 1

Introduction One of the most common and popular methods for cell cycle detection is the use of fluorescence-based dyes. There are a number of fluorescent-based dyes that are capable of binding to double stranded DNA upon cell fixation. Propidium iodide (PI) and DAPI are two such dyes. Since the amount of bound fluorescent dye is directly proportional to the amount of DNA present within a cell, these dyes can be used to detect the cell cycle within a population of cells. How it works: As the cells are going through the cell cycle, the amount of DNA that is contained [...]

By |2021-06-15T20:45:21+00:00April 17th, 2013|Categories: About Cell-Based Assays, Cell Counting Leadership|0 Comments
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