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Extra resources for Advances in Immunoassay Technology
1995). Contribution of antibody heavy chain CDR1 to digoxin binding analyzed by random mutagenesis of phage-displayed Fab 26-10. J Biol Chem, 270(48), 28541-28550. Short, M. , Krykbaev, R. , Jeffrey, P. , & Margolies, M. N. (2002). Complementary combining site contact residue mutations of the anti-digoxin Fab 26-10 permit high affinity wild-type binding. J Biol Chem, 277(19), 16365-16370. Sidhu, S. , Weiss, G. , & Wells, J. A. (2000). High copy display of large proteins on phage for functional selections.
And Marinetti, M. (2001). Enzymatic surface modification of acrylonitrile fibers. Applied Surface Science, Vol. 177, pp. 32-41 Charles, P. , Soto, C. , Goldman, E. , Martin, B. , Rav, R. I. and Taitt, C. R. (2006). A galactose polyacrylate-based hydrogel scaffold for the detection of cholera toxin and staphylococcal enterotoxin B in a sandwich immunoassay format. 578, No. 1, (18 September 2006), pp. 2-10 Che, A. , Nie, F. , Uang, X. , Xu, Z. K. and Yao, K. (2005). Acrylonitrile-based copolymer membranes containing reactive groups: Surface modification by the immobilization of bimolecules.
At 1:8000 conjugate dilutions, thus, these values were established as the optimized concentration and dilution. This indicated that at higher concentration saturation of primary Ab occurred due to Ab-Ab interactions and steric hindrance. 23 for the dilutions 1:2000 to 1:32000 of the conjugate GAR-HRP. Sensitivity is an important parameter while developing any immunogenic assay. The sensitivity of the assay was determined for the modified PAN fibers by varying the concentration of the analyte RAG-IgG.