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Use of an enzyme linked immunosorbent assay (ELISA) for quantification of proteins on the surface of materials

โœ Scribed by Merritt, Katharine ;Edwards, Christopher R. ;Brown, Stanley A.


Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
606 KB
Volume
22
Category
Article
ISSN
0021-9304

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โœฆ Synopsis


This study demonstrates the usefulness of an enzyme linked immunosorbent assay (ELISA) for detection and quantification of protein on the surface of materials. Bovine serum albumin (BSA) and bovine gamma globulin (BGG) were the proteins used. Titanium and stainless steel were the materials tested. The proteins were detected with the use of rabbit antiserum specific for BSA and for BGG. This reaction was quantitated by the use of horseradish pemxidase conjugated goat anti-rabbit gamma globulin. The technique is described in detail.

The technique was demonstrated to be suitable for quantitation oโ‚ฌ protein from 0.01 rng/mL to 0.1 rng/mL on the surface of 3 mm x 10 mm materials. The technique was also demonstrated to be suitable for determining the surface area of solid materials. It is a simple technique and suitable for most biornaterials laboratories.


๐Ÿ“œ SIMILAR VOLUMES


The use of enzyme-linked immunosorbent a
โœ Siong I. Wie; Bruce D. Hammock ๐Ÿ“‚ Article ๐Ÿ“… 1982 ๐Ÿ› Elsevier Science ๐ŸŒ English โš– 707 KB

An enzyme-linked immunosorbent assay (ELISA) for 4-t-octylphenyl ethoxylates such as Triton X-100 was developed. Both the 4-t-octylphenyl and the ethoxylate moiety were required for antibody recognition since members of the Triton N series showed low cross-reactivity, and polyethylene glycol polymer