The aim of this study was to design a resolution typing system for the HLA-B gene. This technique involves a one-step PCR reaction utilizing genomic DNA and sequence-specific primers to determine the specificity of each allele and to produce a larger primer data base ideal for serological analysis. The application of this technique to serological analysis can improve serology detection which is currently hindered by antibody cross-reactivity and the unavailability of useful typing reagents.
Identifer | oai:union.ndltd.org:unt.edu/info:ark/67531/metadc278947 |
Date | 08 1900 |
Creators | Chiu, Angela Chen-Yen |
Contributors | Shanley, Mark Stephen, Benjamin, Robert C., O'Donovan, Gerard A. |
Publisher | University of North Texas |
Source Sets | University of North Texas |
Language | English |
Detected Language | English |
Type | Thesis or Dissertation |
Format | viii, 74 leaves: ill., Text |
Rights | Public, Copyright, Copyright is held by the author, unless otherwise noted. All rights reserved., Chiu, Angela Chen-Yen |
Page generated in 0.0023 seconds