Aflac Cancer Center & Blood Disorder Center 5455 Meridian Marks Rd STE 400, Atlanta, GA 30342 4047853240 (phone), 4047853600 (fax)
Languages:
English Spanish
Description:
Ms. Ballard works in Atlanta, GA and specializes in Pediatric Hematology-Oncology. Ms. Ballard is affiliated with Childrens Heathcare Of Atlanta At Scottish Rite.
Charles Keller - Salt Lake City UT, US Linda Ballard - Salt Lake City UT, US Richard Lemmons - Salt Lake City UT, US
International Classification:
C12Q001/68 C12P019/34
US Classification:
435/006000, 435/091200
Abstract:
A high-throughput assay for characterizing a subject's genetic makeup is disclosed. Specifically a high-throughput assay utilizing PCR is disclosed that permits the rapid and accurate characterization of a subject's inherited alleles of the polymorphic glutathione S-transferase (GST) genes GSTM1, GSTM3, GSTP1, and GSTT1. This method allows detection of the specific alleles inherited, including the gene dosage of GSTM1 and GSTT1 while not requiring restriction endonuclease digestion of the PCR products in order to detect length differences. Further, the method allows all analyses to be performed simultaneously in the same gel lane, thus further adding efficiency and cost-effectiveness.
High Throughput Detection Of Glutathione S-Transferase Polymorphic Alleles
Charles Keller - SALT LAKE CITY UT, US Linda Ballard - Salt Lake City UT, US Richard Lemmons - Salt Lake City UT, US Francis Ali-Osman - Houston TX, US
International Classification:
C12Q 1/68 C12P 19/34
US Classification:
435006000, 435091200
Abstract:
A high-throughput assay for characterizing a subject's genetic makeup is disclosed. Specifically, a high-throughput assay utilizing PCR is disclosed that permits the rapid and accurate characterization of a subject's inherited alleles of the polymorphic glutathione S-transferase (GST) genes GSTM, GSTM, GSTP, and GSTT. This method allows detection of the specific alleles inherited, including the gene dosage of GSTMand GSTTwhile not requiring restriction endonuclease digestion of the PCR products in order to detect length differences. Further, the method allows all analyses to be performed simultaneously in the same gel lane, thus further adding efficiency and cost-effectiveness.