Table 1 of Ahad, Mol Vis 2007; 13:388-396.


Table 1. Primers used in detecting single nucleotide polymorphism in chemokine genes

The single nucleotide polymorphism (SNPs) were detected in 141 patients and 282 controls by sequence specific primers polymerase chain reaction (SSP-PCR) method. SSP-PCR utilizes SSPs with 3'-end mismatches and identifies the presence of specific allelic variants through PCR amplification.

                                                                                  Product
                                                                                   size
       SNP            Chromosome    Identity            Primer (5'-3')             (bp)
-------------------   -----------   ---------   -------------------------------   -------
MCP-1 -2518A/G        17q11.2-q12   rs1024611   F: AAGTGGGAGGCAGACAGCTA/G         252
                                                R: CTGATAAAGCCACAATCCAGAG

RANTES -403G/A        17q11.2-q12   rs2107538   F: CATGGATGAGGGAAAGGAGG/A         285
                                                R: GAGTCTCTGTCTCTCCCTCA

RANTES -28C/G         17q11.2-q12   rs2280788   F: GCCCTTTATAGGGCCAGTTG/C         314
                                                R: GTCCTAACTGCCACTCCTTG

CCR2 V64I             3p21          rs1799864   F: TTTTTGCAGTTTATTAAGATGAGGAC/T   808
                                                R: GAAGGCAGAAGGTGAATAGTTC

CCR5 -59029G/A        3p21          rs2040388   F: ACTTCACATTAACCCTGTGC/T         712
                                                R: ACTGTCATTCAGCCCAATACC

CCR5 32 bp deletion   3p21                      F: GCTCTCATTTTCCATACAGTCAG/A      827/808
                                                R: TATACATAAGGAACTTTCGGAGTG

Ahad, Mol Vis 2007; 13:388-396 <http://www.molvis.org/molvis/v13/a42/>
©2007 Molecular Vision <http://www.molvis.org/molvis/>
ISSN 1090-0535