Coating technologies for Microarrays & Biochips

MicroSurfaces, Inc. enables the MEMS industry

Advanced Surface Technologies for Protein Microarrays, Microfluidics & Biomedical Research

		High density PEG brush to prevent non-specific adsorption; Robust bonds to the surface for long term coating stability; Functional groups for the facile immobilization of proteins; Chemical environment for long-term protein stability & optimal target-probe interaction. Air-stable and fluidic supported lipid microarray for cell membrane microarrays.
		Read the application notes: \| PEG \| Cu2+/PEG \| NHS/PEG \| Biotin/PEG \| Maleimide/PEG \| Membrane microarray \|
		click to read more...	Zero background Cu2+ surface for the immobilization of poly-His taggerd proteins. A microarray of 6xHis tagged protein molecules spotted on the Cu2+/PEG surface. The protein was detected by immunostaining.
		click to read more...	Zero background NHS surface for the immobilization of proteins, peptides, antibody, & other molecules. A microarray of fibrinogen fabricated on NHS/PEG/glass slides and detected by immunostaining.
		click to read more...	Zero background biotin/streptavidin surface for the immobilization of biotinylated molecules. A microarray of biotin-conjugated BSA on the streptavidin/biotin/PEG surface. The immobilized BSA is detected by immonostaining.
		click to read more	Zero background maleimide surface for the immobilization of molecules with -SH functional groups. Fluorescence image of dye-conjugated oligonucleotides with -SH termination covalently linked (hand spotted) on a Maleimide-PEG/glass slide.
		click to read more	Multivalent binding curves of two E-coli strains on mannose density gradient microarrays (see inset). The upper shows two optical microscope images of E-coli cells adsorbed on SLB spots with 1% and 10% mannose, respectively.
		Click here to read more about surface chemistry for protein immobilization.
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