CytoPainter kits-know your subcellular structures

CytoPainter kits-know your subcellular structures

Cell Biology

March 02, 2015

CytoPainter is the ideal platform for multicolor staining that allows you to effectively visualize cellular components and cellular tracking. The main Characteristics and advantages are:

  • Minimal hands-on time - prepare cells, add dye, incubate and analyze
  • Proprietary fluorescent dye with high photostability - minimal photobleaching
  • Available in a variety of colors - ideal for co-localization studies with transfected stable cell lines (such as GFP, tomato or mCherry)
  • Compatible with most common fluorescent microscope filters
  • Suitable for proliferating and non-proliferating suspension and adherent cells

You can track membrane/protein transport through the endomembrane system, visualize actin skeleton structure or cellular mitochondria, as well as labeling and tracing cells to study cellular motility and other cell events in a spatial and temporal context.

You can analyze your cells of interest for hours thanks to our cell tracking dyes that are retained in living cells. The dyes consist of hydrophobic molecules that can permeate through the plasma membrane and become strongly fluorescent once inside the cell. The main Characteristics and advantages are:

  • Proprietary fluorescent tracking dye with high photostability - no photobleaching
  • No efflux from cell - more stable inside the cell than CFSE
  • Can be used in fluorescence microscopy, flow cytometry and microplate reader assays
  • Suitable for proliferating and non-proliferating live suspension and adherent cells
Simple new prenatal blood test for early and accurate detection of major chromosomal abnormalities

Simple new prenatal blood test for early and accurate detection of major chromosomal abnormalities

Cell Biology

Multiplicom is proud to launch Clarigo™, a new CE-IVD1 non-invasive prenatal test (NIPT). This highly accurate blood test will enable genetic analysis laboratories to detect the presence or absence of major chromosomal abnormalities such as trisomy 21 (Down’s syndrome), 18 (Edwards’ syndrome) and 13 (Patau syndrome), in the fetus, as early as in the first trimester of pregnancy by analysis of the fetus’s DNA in the maternal blood.

October 22, 2015 More +
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