Impact of RBC contamination in clinical samples

Bone marrow, cord blood, whole blood, and peripheral blood are routinely processed in many different laboratories. Whether for cryopreservation or for downstream isolation of specific nucleated cells, (such as stem cells, B-cells, or T-cells) accurately measuring cell concentration and viability is paramount to the overall success of the project. Many blood-based samples (whole blood, peripheral blood, bone marrow, PBMC, cord blood, etc…) may contain residual red blood cells even after RBC lysis. (See figure below) When samples are enumerated using manual counting, the presence of residual RBCs can lead to inaccurate cell concentration and viability readings. Nucleic acid dyes, acridine [...]

Trypan Blue vs. Acridine Orange/Propidium Iodide to measure cell viability

Do you have red-blood cells, cell debris, or tissue debris in your samples? When your samples contain unwanted particles use: Acridine Orange/ Propidium Iodide (AO/PI) viability assay to accurately measure the concentration and viability of your samples! AO/PI Protocol Obtain Nexcelom AO/PI solution: Cat # CS2-0106-5ML Stain cell sample at 1:1 with AO/PI solution Load counting chamber slide with 20 µl of cells and analyze Report Accurate and Consistent concentration and viability Results Do you have clean cell samples without RBCs, or other cell debris? When your samples are free from unwanted particles, Use Trypan Blue exclusion assay to accurately [...]

By |2021-06-15T20:44:07+00:00December 20th, 2013|Categories: Cell Counting Leadership, Cellometer Application News|0 Comments

Automate Hemacytometer … Now Even Faster and Easier

Cellometer Bright Field Cell Counters Cellometer Bright Field Cell Counters   Cell count and trypan blue viability in <10 seconds! Proprietary Cell Membrane Outline Algorithm to count irregular shaped cells, cells in clusters and produce cell size histograms View, print, and save counted cell images, data reports, and cell size histograms Find the Cellometer Cell Counter for Your Lab All-In-One System. Cellometer Auto 1000 A convenient stand-alone system with a large, userfriendly touch screen. Proven Performance. Cellometer Auto T4 Used by all 40 NCI comprehensive cancer centers and the top 10 pharmaceutical companies. Affordable. Cellometer Mini The most [...]

By |2023-03-16T14:05:13+00:00July 15th, 2013|Categories: Cell Counting Leadership, Cellometer Product News|0 Comments

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

Image cytometry method for autophagy activity detection in living cells

Cellometer Vision Image Cytometer was used to capture and identify fluorescent positive GFP-LC3 cells. Autophagy is an important cellular catabolic process that plays a variety of important roles, including maintenance of the amino acid pool during starvation, recycling of damaged proteins and organelles, and clearance of intracellular microbes. First, the damaged proteins, organelles or foreign microbes are isolated by double membrane vesicles called autophagosomes.  The vesicles then complete the enclosure of the damaged organelles and then fuses with lysosome. to form autolysosomes.  Finally, the materials are degraded within the autolysosomes and the nutrients are recycled back to the [...]

By |2021-06-15T20:44:50+00:00June 10th, 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

Accurate Measurement of Peripheral Blood Mononuclear Cell Concentration using Image Cytometry to Eliminate RBC-Induced Counting Errors

Peripheral blood mononuclear cells (PBMCs) have been widely researched in the fields of immunology, infectious disease, oncology, transplantation, hematological malignancy, and vaccine development. Specifically, in immunology research, PBMCs have been utilized to monitor concentration, viability, proliferation, and cytokine production from immune cells, which are critical for both clinical trials and biomedical research. […]

By |2021-06-15T20:45:44+00:00January 23rd, 2013|Categories: About Cells, Cell Counting Leadership|0 Comments

10 Questions to Ask Before Purchasing an Automated Cell Counter

Ten Questions to Ask Before Purchasing an Automated Cell Counter Believe it or not, all cell counters are not created equally. Ask a colleague with a handheld counter that sits in a drawer or a bench-top cell counter that acts as a paperweight and they will tell you that some cell counters don’t work as expected. Before purchasing an automated cell counter, ask the representative the following questions. Knowing these answers will help ensure that you purchase the right cell counter for your applications. […]

By |2021-06-15T20:45:52+00:00November 27th, 2012|Categories: Cell Counting Leadership, Cellometer Product News|0 Comments
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