Merase Chain Reaction (qRTPCR) AnalysisReactions were conducted on a Rotor-GeneTM 6000 (Corbett Research, Sydney, NSW, Australia) using a SuperScriptTM III PlatinumH SYBRH Green One-Step qRT-PCR kit (Invitrogen Corporation). The reactions were prepared according to standard protocols. Reaction mixture contained 50 ng of total RNA from each sample, 1.0 mM 25033180 of each primer, 12.5 mL of 2X SYBRH Green Reaction Mix and 0.5 mL of SuperScriptTM III RT/ PlatinumH Taq Mix to a final volume of 25 mL. Negative samples were run for each qRT-PCR assay consisting of no RNA in the reverse transcriptase reaction and no cDNA in the PCR. Reactions were carried out under the following cycling conditions: 50uC for 30 min, 95uC for 15 min, and 40 cycles of 95uC for 20 s, followed by 56uC for 30 s and 72uC for 30 s before a final primer sequence extension incubation at 72uC for 5 min. Fluorescence changes were monitored after each cycle, and Terlipressin site melting curve analysis was performed at the end of cycles to verify PCR product identity (72uC ramping to 99uC at 0.2uC/second with continuous fluorescence readings). Specificity of amplicons was also ensuredby agarose gel electrophoresis to visualize a unique product fragment of appropriate size. Gene-specific primer pairs were located on two adjacent exons to achieve a high level of specificity and to avoid detection of genomic DNA. Primers were designed to have similar GC content and melting temperatures using the Primer3_cgi v 0.2 program. The nucleotide sequences for the primers were: Caspase 3 (NM_009810.2) forward 59- TGA CTG GAA AGC CGA AAC TC 39 and reverse 59- AGC CTC CAC CGG TAT CTT CTV39; Caspase 8 (NM_009812.2) forward 59- CCG AGC TGG ACT TGT GACC -39 and reverse 59- CTG CCC AGT TCT TCA GCA AT-39 and HPRT (NM_013556.2) forward 59 CTT CCT CCT CAG ACC GCT TT -39 and reverse 59- TTT VCCA AAT CCT CGG CAT AA – 39. 125-65-5 manufacturer Amplified fragment sizes were 122, 118 and 145 bp for Caspase 3, Caspase 8 and HPRT, respectively. To evaluate the amplification efficiency of each target and housekeeping gene (HPRT), standard curves were constructed from a reference sample of RNA using duplicate serial dilutions at five 
different RNA concentrations (0.8, 4, 20, 100, and 500 ng/mL). qRT-PCR quantification of expression of the target gene in tumorApoptosis in Melanoma Cells after BNCTFigure 6. Melanoma cell death after BNCT. (A) Tumor volume of mice bearing B16F10 melanoma during twenty-one days. On the fourteenth day after B16F10 melanoma implantation, the BNCT group received BPA and was irradiated with thermal neutrons. The mice were sacrificed and analyzed 1 or 7 days after BNCT treatment. (B) Western blotting analyses of caspase 3, 7, 8, 9, Bcl-2 and Bax in melanoma tissue. (C, D) mRNA expression levels of caspase 3 and 8, respectively, quantified by RT-PCR. doi:10.1371/journal.pone.0059639.gsamples was accomplished by measuring the fractional cycle number at which the magnitude of expression reached a fixed threshold 16574785 (CT = 0.02974) directly related to the amount of PCR product. The mathematical method used was the model described by Pfaffl et al [17], since the amplification efficiencies of the target gene and reference were not equivalent.Tissue Preparation and Immunohistochemical AnalysisAll tumor tissues were fixed in 10 neutral buffered formalin and embedded in paraffin. Thin sections were stained with hematoxylin and eosin. Additional subserial sections from all the paraffin blocks were used for immunohistochemistry. The antibo.Merase Chain Reaction (qRTPCR) AnalysisReactions were conducted on a Rotor-GeneTM 6000 (Corbett Research, Sydney, NSW, Australia) using a SuperScriptTM III PlatinumH SYBRH Green One-Step qRT-PCR kit (Invitrogen Corporation). The reactions were prepared according to standard protocols. Reaction mixture contained 50 ng of total RNA from each sample, 1.0 mM 25033180 of each primer, 12.5 mL of 2X SYBRH Green Reaction Mix and 0.5 mL of SuperScriptTM III RT/ PlatinumH Taq Mix to a final volume of 25 mL. Negative samples were run for each qRT-PCR assay consisting of no RNA in the reverse transcriptase reaction and no cDNA in the PCR. Reactions were carried out under the following cycling conditions: 50uC for 30 min, 95uC for 15 min, and 40 cycles of 95uC for 20 s, followed by 56uC for 30 s and 72uC for 30 s before a final primer sequence extension incubation at 72uC for 5 min. Fluorescence changes were monitored after each cycle, and melting curve analysis was performed at the end of cycles to verify PCR product identity (72uC ramping to 99uC at 0.2uC/second with continuous fluorescence readings). Specificity of amplicons was also ensuredby agarose gel electrophoresis to visualize a unique product fragment of appropriate size. Gene-specific primer pairs were located on two adjacent exons to achieve a high level of specificity and to avoid detection of genomic DNA. Primers were designed to have similar GC content and melting temperatures using the Primer3_cgi v 0.2 program. The nucleotide sequences for the primers were: Caspase 3 (NM_009810.2) forward 59- TGA CTG GAA AGC CGA AAC TC 39 and reverse 59- AGC CTC CAC CGG TAT CTT CTV39; Caspase 8 (NM_009812.2) forward 59- CCG AGC TGG ACT TGT GACC -39 and reverse 59- CTG CCC AGT TCT TCA GCA AT-39 and HPRT (NM_013556.2) forward 59 CTT CCT CCT CAG ACC GCT TT -39 and reverse 59- TTT VCCA AAT CCT CGG CAT AA – 39. Amplified fragment sizes were 122, 118 and 145 bp for Caspase 3, Caspase 8 and HPRT, respectively. To evaluate the amplification efficiency of each target and housekeeping gene (HPRT), standard curves were 
constructed from a reference sample of RNA using duplicate serial dilutions at five different RNA concentrations (0.8, 4, 20, 100, and 500 ng/mL). qRT-PCR quantification of expression of the target gene in tumorApoptosis in Melanoma Cells after BNCTFigure 6. Melanoma cell death after BNCT. (A) Tumor volume of mice bearing B16F10 melanoma during twenty-one days. On the fourteenth day after B16F10 melanoma implantation, the BNCT group received BPA and was irradiated with thermal neutrons. The mice were sacrificed and analyzed 1 or 7 days after BNCT treatment. (B) Western blotting analyses of caspase 3, 7, 8, 9, Bcl-2 and Bax in melanoma tissue. (C, D) mRNA expression levels of caspase 3 and 8, respectively, quantified by RT-PCR. doi:10.1371/journal.pone.0059639.gsamples was accomplished by measuring the fractional cycle number at which the magnitude of expression reached a fixed threshold 16574785 (CT = 0.02974) directly related to the amount of PCR product. The mathematical method used was the model described by Pfaffl et al [17], since the amplification efficiencies of the target gene and reference were not equivalent.Tissue Preparation and Immunohistochemical AnalysisAll tumor tissues were fixed in 10 neutral buffered formalin and embedded in paraffin. Thin sections were stained with hematoxylin and eosin. Additional subserial sections from all the paraffin blocks were used for immunohistochemistry. The antibo.