DUAL FUNCTIONALITY: MyQuVigen nanoparticles combine superparamagnetic iron oxide with quantum dots, providing high magnetic moment for easy separation and bright stable fluorescence at 535 nm emission for extensive imaging applications
UNIVERSAL BINDING: Streptavidin-conjugated fluorescent magnetic nanoparticles universally bind to any biotin-conjugated antibody, enabling versatile cell isolation and labeling with mouse antibodies for CTCs, stem cells, and other cell populations
OPTIMAL FLUORESCENCE: Maximal fluorescence emission at 535 nm with excitation wavelength of 488 nm or shorter, delivering strong and long-lasting fluorescent signals for microscope imaging and fluorescence-based cell analysis
GENTLE MAGNETIC SEPARATION: Column-free cell separation using a magnetic rack eliminates mechanical stress on cells, preserving high viability for downstream applications including cell culture, mRNA isolation, and RT-PCR analysis
HIGH PERFORMANCE: Features high binding capacity, low non-specific binding, and excellent biocompatibility, ensuring consistent high-quality results with highly purified viable cells ready for immediate use
Description
MyQuVigen nanoparticles represent a breakthrough in cell separation technology, combining superparamagnetic iron oxide with quantum dots for superior performance. These fluorescent magnetic nanoparticles feature streptavidin conjugates with peak emission at 615 nm, offering bright, stable fluorescence and strong magnetic properties. The particles can be excited at 488 nm or shorter wavelengths, making them versatile for various imaging applications. Perfect for cell isolation and labeling, these nanoparticles enable column-free magnetic separation, preserving cell viability for downstream analysis. The streptavidin coating allows universal binding to biotin-conjugated antibodies with high specificity and binding capacity. Researchers can achieve consistent, high-quality results in cell separation and fluorescence imaging applications. The nanoparticles are ideal for isolating specific cell populations like CTCs and stem cells, with the separated cells remaining viable for further culture or molecular analysis. The strong fluorescent signal enables direct microscope imaging and fluorescence-based cell analysis without additional processing steps.