Saturday, May 15, 2004 Description NGFR TaqI(a) Polymorphism Procedure TaqI(a) (7.18 KB DWST OF EXON 6) Template: Genomic DNA 100-200 ng/reaction Primer 1. NGFRTQAF1 5' GAC ACT GGT TAT ACT CTA GTC C 3' 100 ng/reaction Primer 2. NGFRTQAR1 5...
Description DRD2 TaqI "A" Polymorphism Procedure Taq I "A" Located 10 kb downstream from exon 8 TEMPLATE: Genomic DNA 100-200 ng/reaction volume of 25 l. Primer 1: 5014 MOD: '5- CCT TCC TGA GTG TCA TCA AC 100 ng/reaction Primer 2: TAQACK1:...
Saturday, May 15, 2004 Description RBP3 BglII Polymorphism Procedure Bgl II polymorphism located near 5' end of intron 2 Genomic DNA: 100-200 ng/reaction volume of 25 ul Primer 1. RBP3BGL1: 5'-ACC CTG TGA CAC AGC AGA GG-3' 100 ng/Reaction...
Description DRD2 TaqI "B" Polymorphismq Procedure Taq I "B" Bcl I Located in intron 1, approximately 1 kb upstream from exon 2 (The Taq I "B" and the Bcl I sites are 12 bp apart) Template: Genomic DNA 100-200 ng/ reaction volume of 25 l. P...
Saturday, May 15, 2004 Description RBP3 MspI Polymorphism Procedure MspI Polymorphism located near 3' end of intron 1 Template: Genomic DNA 100-200 ng/reaction volume of 25 ul Primer 1. RBP3MSP3: 5'- CTG TAA GAG TTG GAG GT-3' 100 ng/Rx Pri...
Saturday, May 15, 2004 Description D10S94 PvuII Polymorphism Procedure Pvu II Template: Genomic DNA 100-200 ng/reaction volume of 25 l Primer 1. S94PVUA 5 -AGCTCACCCAGATCCTAA -3' 90 ng/reaction Primer 2. S94PVUB 5' -CCTCCCTTCAGTAGACAC -3'...
Saturday, May 15, 2004 Description ACADM TaqI Polymorphism Procedure TaqI site (located in intron 7) Template: Genomic DNA 100-200 ng/reaction volume of 25 l Primer 1. ACADMTAQI: 5'-GAT CCA GTG ACT CAG AAG-3' 100 ng/reaction Primer 2. ACAD...
Saturday, May 15, 2004 Description DM1 Alu Polymorphism Procedure Template: Genomic DNA 100-200 ng/reaction volume of 25 ul Primer 1: 405: 5'-CTG TAT ACT CAG CTA CTA GGG T-3' 50 ng/rx Primer 2: 491: 5'-AAA TAG GCT GGA CCG CGG-3' 50 ng/rx P...
Thursday, November 20, 2003 Description For Double-stranded reactions Procedure 1. Add the following to a 1.5 ml microcentrifuge tube: 5 ulds DNA (5 ug) 4 ul1 N NaOH 3 ulddH2O 12 ul 2. Incubate the reaction at 65-70degC for 5 minutes, and...
Thursday, November 20, 2003 Description One of the major problems in DNA cycle sequencing is that when fluorescent primers are used the reaction conditions are such that the nested fragment set distribution is highly dependent upon the tem...