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Corning® Assay Surfaces:
NBS™ Coated Surface

Some assays and procedures require a surface that is nonbinding because many proteins, enzymes in particular, may become activated or inactivated upon attachment to a surface. Corning's unique NBS™ treatment (U.S. Patents 6,093,559 and 6,319,664) creates a nonionic hydrophilic surface (polyethylene oxide [PEO]-like) that minimizes molecular interactions (Figure 1). Since proteins and other biomolecules passively adsorb to surfaces primarily through hydrophobic and ionic interactions, the NBS™ surface lacking these characteristics naturally inhibits nonspecific immobilization via these forces.

Figure 1. PEO chains immobilized on polystyrene create the nonionic hydrophilic NBS™ surface that minimizes molecular binding.
















Results (Table 1) show the NBS™ surface has the ability to significantly reduce (<2 ng/cm2) protein and nucleic acid binding to microplates, while maintaining enzyme activity. The nonionic, hydrophilic NBS™ surface is therefore well suited for enhancement of signal-to-noise in homogeneous assays such as Scintillation Proximity Assay (SPA). NBS™ surfaces are stable to aqueous biological fluids and biological reagents containing up to 20% isopropyl alcohol or DMSO or 10 M urea or 1% SDS, and over a pH range (3-11).

Table 1. Comparison of protein and nucleic acid binding with various polymers
Binding in ng/cm2
125I-IgG
125I-BSA
125I-Insulin
32P-oligoDNA
32P-l phageDNA
Polystyrene (PS)
400
450
310
22
6
Polypropylene 380
380
440
370
3
<2
NBS on PS
<2.5
<2.5
5
<2
<2
Based on a Scintillation Proximity Assay (SPA) using 100 µL/well in 96 well microplates. Contents were aspirated and washed 3 times with 200 µL/well of PBS, pH 7.4.

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