iplex-gold mastermix (Sequenom)
90
Structured Review
Sequenom
iplex-gold mastermix
Iplex Gold Mastermix, supplied by Sequenom, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/iplex-gold+mastermix/iplex+gold+mastermix/pmc03130784-135-38-40
Average 90 stars, based on 1 article reviews
Iplex Gold Mastermix, supplied by Sequenom, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/iplex-gold+mastermix/iplex+gold+mastermix/pmc03130784-135-38-40
Average 90 stars, based on 1 article reviews
iplex-gold mastermix - by Bioz Stars,
2026-09
90/100 stars
Images
Related Articles
Detection Assay:Article Title: Transcriptome Sequencing, and Rapid Development and Application of SNP Markers for the Legume Pod Borer Maruca vitrata (Lepidoptera: Crambidae) Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the Article Title: Transcriptome sequencing, and rapid development and application of SNP markers for the legume pod borer Maruca vitrata (Lepidoptera: Crambidae). Article Snippet: Each SNP genotyping assay was performed on a Sequenom MassARRAYH, and consisted of an initial PCR step that amplified the genome region that contains an individual SNP, followed by a single base extension reaction that incorporated PLoS ONE | www.plosone.org 3 July 2011 | Volume 6 | Issue 7 | e21388 mass-modified dideoxynucleotides that are complementary to the polymorphic locus within each allele included in the iPLEX-Gold mastermix (Sequenom, San Diego, CA; Tang et al. 2004). Article Title: The Application and Performance of Single Nucleotide Polymorphism Markers for Population Genetic Analyses of Lepidoptera Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the Article Title: Transcriptome sequencing, and rapid development and application of SNP markers for the legume pod borer Maruca vitrata (Lepidoptera: Crambidae). Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the iPLEX-Gold mastermix (Sequenom; [58]). Article Title: Influence of host plant, geography and pheromone strain on genomic differentiation in sympatric populations of Ostrinia nubilalis. Article Snippet: In brief, loci containing a priori defined SNPs were amplified in four PCR multiplexes (W1, W2, W3 and W4; Coates et al., 2011), and subsequently used as template for SBE as‐ says that incorporated allele‐specific mass‐modified dideoxynucleo‐ tides using the iPLEX‐Gold Mastermix (Sequenom; Tang et al., 1999). Article Title: The application and performance of single nucleotide polymorphism markers for population genetic analyses of lepidoptera. Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the iPLEX-Gold mastermix (Sequenom; Tang et al., 1999). Article Title: Transcriptome Sequencing, and Rapid Development and Application of SNP Markers for the Legume Pod Borer Maruca vitrata (Lepidoptera: Crambidae) Article Snippet: Each SNP genotyping assay was performed on a Multiplex Assay:Article Title: Transcriptome Sequencing, and Rapid Development and Application of SNP Markers for the Legume Pod Borer Maruca vitrata (Lepidoptera: Crambidae) Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the Article Title: Transcriptome sequencing, and rapid development and application of SNP markers for the legume pod borer Maruca vitrata (Lepidoptera: Crambidae). Article Snippet: Each SNP genotyping assay was performed on a Sequenom MassARRAYH, and consisted of an initial PCR step that amplified the genome region that contains an individual SNP, followed by a single base extension reaction that incorporated PLoS ONE | www.plosone.org 3 July 2011 | Volume 6 | Issue 7 | e21388 mass-modified dideoxynucleotides that are complementary to the polymorphic locus within each allele included in the iPLEX-Gold mastermix (Sequenom, San Diego, CA; Tang et al. 2004). Article Title: The Application and Performance of Single Nucleotide Polymorphism Markers for Population Genetic Analyses of Lepidoptera Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the Article Title: Transcriptome sequencing, and rapid development and application of SNP markers for the legume pod borer Maruca vitrata (Lepidoptera: Crambidae). Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the iPLEX-Gold mastermix (Sequenom; [58]). Article Title: Influence of host plant, geography and pheromone strain on genomic differentiation in sympatric populations of Ostrinia nubilalis. Article Snippet: In brief, loci containing a priori defined SNPs were amplified in four PCR multiplexes (W1, W2, W3 and W4; Coates et al., 2011), and subsequently used as template for SBE as‐ says that incorporated allele‐specific mass‐modified dideoxynucleo‐ tides using the iPLEX‐Gold Mastermix (Sequenom; Tang et al., 1999). Article Title: The application and performance of single nucleotide polymorphism markers for population genetic analyses of lepidoptera. Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the iPLEX-Gold mastermix (Sequenom; Tang et al., 1999). Article Title: Transcriptome Sequencing, and Rapid Development and Application of SNP Markers for the Legume Pod Borer Maruca vitrata (Lepidoptera: Crambidae) Article Snippet: Each SNP genotyping assay was performed on a Polymerase Chain Reaction:Article Title: Transcriptome Sequencing, and Rapid Development and Application of SNP Markers for the Legume Pod Borer Maruca vitrata (Lepidoptera: Crambidae) Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the Article Title: Transcriptome sequencing, and rapid development and application of SNP markers for the legume pod borer Maruca vitrata (Lepidoptera: Crambidae). Article Snippet: Each SNP genotyping assay was performed on a Sequenom MassARRAYH, and consisted of an initial PCR step that amplified the genome region that contains an individual SNP, followed by a single base extension reaction that incorporated PLoS ONE | www.plosone.org 3 July 2011 | Volume 6 | Issue 7 | e21388 mass-modified dideoxynucleotides that are complementary to the polymorphic locus within each allele included in the iPLEX-Gold mastermix (Sequenom, San Diego, CA; Tang et al. 2004). Article Title: The Application and Performance of Single Nucleotide Polymorphism Markers for Population Genetic Analyses of Lepidoptera Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the Article Title: Transcriptome sequencing, and rapid development and application of SNP markers for the legume pod borer Maruca vitrata (Lepidoptera: Crambidae). Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the iPLEX-Gold mastermix (Sequenom; [58]). Article Title: Influence of host plant, geography and pheromone strain on genomic differentiation in sympatric populations of Ostrinia nubilalis. Article Snippet: In brief, loci containing a priori defined SNPs were amplified in four PCR multiplexes (W1, W2, W3 and W4; Coates et al., 2011), and subsequently used as template for SBE as‐ says that incorporated allele‐specific mass‐modified dideoxynucleo‐ tides using the iPLEX‐Gold Mastermix (Sequenom; Tang et al., 1999). Article Title: The application and performance of single nucleotide polymorphism markers for population genetic analyses of lepidoptera. Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the iPLEX-Gold mastermix (Sequenom; Tang et al., 1999). Article Title: Transcriptome Sequencing, and Rapid Development and Application of SNP Markers for the Legume Pod Borer Maruca vitrata (Lepidoptera: Crambidae) Article Snippet: Each SNP genotyping assay was performed on a SNP Genotyping Assay:Article Title: Transcriptome Sequencing, and Rapid Development and Application of SNP Markers for the Legume Pod Borer Maruca vitrata (Lepidoptera: Crambidae) Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the Article Title: Transcriptome sequencing, and rapid development and application of SNP markers for the legume pod borer Maruca vitrata (Lepidoptera: Crambidae). Article Snippet: Each SNP genotyping assay was performed on a Sequenom MassARRAYH, and consisted of an initial PCR step that amplified the genome region that contains an individual SNP, followed by a single base extension reaction that incorporated PLoS ONE | www.plosone.org 3 July 2011 | Volume 6 | Issue 7 | e21388 mass-modified dideoxynucleotides that are complementary to the polymorphic locus within each allele included in the iPLEX-Gold mastermix (Sequenom, San Diego, CA; Tang et al. 2004). Article Title: The Application and Performance of Single Nucleotide Polymorphism Markers for Population Genetic Analyses of Lepidoptera Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the Article Title: Transcriptome sequencing, and rapid development and application of SNP markers for the legume pod borer Maruca vitrata (Lepidoptera: Crambidae). Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the iPLEX-Gold mastermix (Sequenom; [58]). Article Title: Influence of host plant, geography and pheromone strain on genomic differentiation in sympatric populations of Ostrinia nubilalis. Article Snippet: In brief, loci containing a priori defined SNPs were amplified in four PCR multiplexes (W1, W2, W3 and W4; Coates et al., 2011), and subsequently used as template for SBE as‐ says that incorporated allele‐specific mass‐modified dideoxynucleo‐ tides using the iPLEX‐Gold Mastermix (Sequenom; Tang et al., 1999). Article Title: The application and performance of single nucleotide polymorphism markers for population genetic analyses of lepidoptera. Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the iPLEX-Gold mastermix (Sequenom; Tang et al., 1999). Article Title: Transcriptome Sequencing, and Rapid Development and Application of SNP Markers for the Legume Pod Borer Maruca vitrata (Lepidoptera: Crambidae) Article Snippet: Each SNP genotyping assay was performed on a Amplification:Article Title: Transcriptome Sequencing, and Rapid Development and Application of SNP Markers for the Legume Pod Borer Maruca vitrata (Lepidoptera: Crambidae) Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the Article Title: Transcriptome sequencing, and rapid development and application of SNP markers for the legume pod borer Maruca vitrata (Lepidoptera: Crambidae). Article Snippet: Each SNP genotyping assay was performed on a Sequenom MassARRAYH, and consisted of an initial PCR step that amplified the genome region that contains an individual SNP, followed by a single base extension reaction that incorporated PLoS ONE | www.plosone.org 3 July 2011 | Volume 6 | Issue 7 | e21388 mass-modified dideoxynucleotides that are complementary to the polymorphic locus within each allele included in the iPLEX-Gold mastermix (Sequenom, San Diego, CA; Tang et al. 2004). Article Title: The Application and Performance of Single Nucleotide Polymorphism Markers for Population Genetic Analyses of Lepidoptera Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the Article Title: Transcriptome sequencing, and rapid development and application of SNP markers for the legume pod borer Maruca vitrata (Lepidoptera: Crambidae). Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the iPLEX-Gold mastermix (Sequenom; [58]). Article Title: Influence of host plant, geography and pheromone strain on genomic differentiation in sympatric populations of Ostrinia nubilalis. Article Snippet: In brief, loci containing a priori defined SNPs were amplified in four PCR multiplexes (W1, W2, W3 and W4; Coates et al., 2011), and subsequently used as template for SBE as‐ says that incorporated allele‐specific mass‐modified dideoxynucleo‐ tides using the iPLEX‐Gold Mastermix (Sequenom; Tang et al., 1999). Article Title: The application and performance of single nucleotide polymorphism markers for population genetic analyses of lepidoptera. Article Snippet: Each SNP detection assay consists of an initial multiplex PCR step that amplifies genome regions containing mutations, followed by a single base extension reaction that incorporates mass-modified dideoxynucleotides complementary to the allele at each polymorphic locus using the iPLEX-Gold mastermix (Sequenom; Tang et al., 1999). Article Title: Transcriptome Sequencing, and Rapid Development and Application of SNP Markers for the Legume Pod Borer Maruca vitrata (Lepidoptera: Crambidae) Article Snippet: Each SNP genotyping assay was performed on a |