Ks. `+’ and `2′ indicate strand specificity of the primers; N+, normal peak

Ks. `+’ and `2′ indicate strand specificity of the primers; N+, normal peak generated from `+’ primer; M+, mutant peak generated from `+’ primer; N2, normal peak generated from `2′ primer; M2, mutant peak generated from `2′ primer. Asterisks mark peaks that are lower than normal due to interference from genetic variations within the primer-hybridizing template sequence. doi:10.1371/journal.pone.0048167.gPrimer Design and OptimizationAll primer sequences are listed in Table 2 and Table S2. We used the information deposited to the dbSNP database [47] to verify that the primers amplifying the HBB fragment encompassing all mutations included in the assay hybridize to invariable sequences. For the design of the primer extension mix, oligonucleotide melting temperatures were calculated using the RaW-probe program available at www.mlpa.com/support (Table S1). Secondary Pentagastrin manufacturer structures and potential primer dimers were predicted using the UNAFold/mfold server at http://mfold.rna.albany.edu/ , applications Homodimer simulations and Hybridization of two different strands [48?0]. To achieve electrophoretic resolution of the multiplexed extension products, oligos expected to carry the same label were set to differ by a minimum of 3 nucleotides. Oligo(dC) 59-non-homologous tails were used to adjust the size of primers longer than 30 nucleotides, keeping the melting temperatures of the sequences complementary to the template within a range of several degrees (Table S1). All oligonucleotides were synthesized and purified by standard desalting at IDT. The observed length of a labeled extension product can deviate from its actual size since electrophoretic mobility is influenced by both sequence and label. For this reasonthe identity of the peaks was confirmed experimentally by exclusion of individual primers from the mix. Initially, the relatively large deviation of the mobility of one product (IVS-I6+) resulted in poor resolution of two fragments carrying identical labels. This was corrected through redesigning the length of several primers and re-running the test to ensure good distribution of the products. Finally, primer concentrations were empirically adjusted to balance peak heights.Single-nucleotide Primer ExtensionA 1856 bp HBB fragment was amplified by PCR (for primer sequences see Table S2) in a mix containing 50 mM Tris-HCl, pH 9.2, 16 mM (NH4)2SO4, 0.1 Tween 20, 2 mM MgCl2, 200 mM each dNTP, 200 nM each forward and reverse primer, and 1.2 U Tth polymerase [51] in a final volume of 25 or 50 ml. Cycling conditions were: initial `hot-start’ denaturation at 95uC for 10 min followed by 35 cycles of 95uC for 30 s, 58uC for 1 min, 68uC for 1 min 45 s, and a final extension at 68uC for 7 min. A 1.4 ml aliquot of the completed reaction typically containing 5?20 ng specific product was then treated with 0.6 ml Exonuclease I and Shrimp get 86168-78-7 Alkaline Phosphatase mix (ExoSAP-IT, USB) for 15 min at 37uC to eliminate unincorporated nucleotide triphosphates and excess PCR primers. The enzymes were heatGenotyping Mediterranean HBB Gene Mutationsinactivated at 86uC 16574785 for 20 minutes and the purified PCR product was directly used as template in a primer extension reaction containing the mutation-specific primer cocktail. For the extension reaction, we used the ABI PRISM SNaPshot Multiplex Kit (Life Technologies) following manufacturer’s instructions except that we reduced the reaction volume and diluted the mix supplying the DNA polymerase and fluorescently labeled termin.Ks. `+’ and `2′ indicate strand specificity of the primers; N+, normal peak generated from `+’ primer; M+, mutant peak generated from `+’ primer; N2, normal peak generated from `2′ primer; M2, mutant peak generated from `2′ primer. Asterisks mark peaks that are lower than normal due to interference from genetic variations within the primer-hybridizing template sequence. doi:10.1371/journal.pone.0048167.gPrimer Design and OptimizationAll primer sequences are listed in Table 2 and Table S2. We used the information deposited to the dbSNP database [47] to verify that the primers amplifying the HBB fragment encompassing all mutations included in the assay hybridize to invariable sequences. For the design of the primer extension mix, oligonucleotide melting temperatures were calculated using the RaW-probe program available at www.mlpa.com/support (Table S1). Secondary structures and potential primer dimers were predicted using the UNAFold/mfold server at http://mfold.rna.albany.edu/ , applications Homodimer simulations and Hybridization of two different strands [48?0]. To achieve electrophoretic resolution of the multiplexed extension products, oligos expected to carry the same label were set to differ by a minimum of 3 nucleotides. Oligo(dC) 59-non-homologous tails were used to adjust the size of primers longer than 30 nucleotides, keeping the melting temperatures of the sequences complementary to the template within a range of several degrees (Table S1). All oligonucleotides were synthesized and purified by standard desalting at IDT. The observed length of a labeled extension product can deviate from its actual size since electrophoretic mobility is influenced by both sequence and label. For this reasonthe identity of the peaks was confirmed experimentally by exclusion of individual primers from the mix. Initially, the relatively large deviation of the mobility of one product (IVS-I6+) resulted in poor resolution of two fragments carrying identical labels. This was corrected through redesigning the length of several primers and re-running the test to ensure good distribution of the products. Finally, primer concentrations were empirically adjusted to balance peak heights.Single-nucleotide Primer ExtensionA 1856 bp HBB fragment was amplified by PCR (for primer sequences see Table S2) in a mix containing 50 mM Tris-HCl, pH 9.2, 16 mM (NH4)2SO4, 0.1 Tween 20, 2 mM MgCl2, 200 mM each dNTP, 200 nM each forward and reverse primer, and 1.2 U Tth polymerase [51] in a final volume of 25 or 50 ml. Cycling conditions were: initial `hot-start’ denaturation at 95uC for 10 min followed by 35 cycles of 95uC for 30 s, 58uC for 1 min, 68uC for 1 min 45 s, and a final extension at 68uC for 7 min. A 1.4 ml aliquot of the completed reaction typically containing 5?20 ng specific product was then treated with 0.6 ml Exonuclease I and Shrimp Alkaline Phosphatase mix (ExoSAP-IT, USB) for 15 min at 37uC to eliminate unincorporated nucleotide triphosphates and excess PCR primers. The enzymes were heatGenotyping Mediterranean HBB Gene Mutationsinactivated at 86uC 16574785 for 20 minutes and the purified PCR product was directly used as template in a primer extension reaction containing the mutation-specific primer cocktail. For the extension reaction, we used the ABI PRISM SNaPshot Multiplex Kit (Life Technologies) following manufacturer’s instructions except that we reduced the reaction volume and diluted the mix supplying the DNA polymerase and fluorescently labeled termin.