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Applied Biosystems™ Custom TaqMan™ SNP Genotyping Assay, non-human

Applied Biosystems TaqMan SNP Genotyping Assays use TaqMan 5'‐nuclease chemistry to amplify and detect specific polymorphisms in purified genomic DNA samples.
Marca: Applied Biosystems™ 4332075
948.10 EUR hasta el 2025-08-24
Use el código promocional "24117" para aplicar la oferta.
Alertas:
Para beneficiarse del descuento, los clientes deben comprar tres unidades del mismo producto al precio de catálogo en un solo pedido para recibir el 33.33% de descuento No hay límite para los múltiplos de 3 que los clientes pueden comprar PCODE:24112
Includes: Dos cabadores de PCR sin etiquetar: directo e inverso (cebadores a 900 nM de concentración final); 1 colorante VIC: La sonda con etiqueta MGB detecta la secuencia del alelo 1 (sondas a una concentración final de 200 Nm); 1 colorante 6FAM: la sonda con etiqueta MGB detecta la secuencia del alelo 2 (sondas a concentración final de 200 nM)
Descripción
Applied Biosystems TaqMan SNP Genotyping Assays use TaqMan 5'‐nuclease chemistry to amplify and detect specific polymorphisms in purified genomic DNA samples. Each assay enables genotyping of individuals for a single nucleotide polymorphism (SNP) and consists of two sequence-specific primers and two TaqMan minor groove binder (MGB) probes with non-fluorescent quenchers (NFQ). One probe is labeled with VIC dye to detect the Allele 1 sequence; the second probe is labeled with FAM dye to detect the Allele 2 sequence.
Custom TaqMan SNP Genotyping Assays can be easily designed at no extra charge by submitting target sequences confidentially to our secure Custom Assay Design Tool. The tool can generate assay designs targeting any SNP in any organism, offering maximum flexibility to meet your research needs.
Benefits:
- Proven—gold-standard TaqMan chemistry and robust assay designs deliver accurate, reproducible, and reliable results
- Easy—convenient single-tube format and simple workflow provide an easy path to trusted results; no optimization required
- Flexible—obtain assay designs for any SNP in any organism using our secure Custom Assay Design Tool, at no extra charge
- Tested—all custom assays are quality-control tested for synthesis accuracy and formulation completeness
Approximate ship time
4–6 days in North America and 6–10 days in Europe
The free Custom Assay Design Tool can generate assays for the detection of SNPs, MNPs, and indels of up to six bases. These custom assays are designed, synthesized, formulated, optimized, and quality control tested.
TaqMan SNP Genotyping Assays require only three reaction components for PCR: purified genomic DNA (1–20 ng), the assay solution, and TaqMan Genotyping Master Mix (or another compatible master mix) (sold separately).
All assay designs are the product of our industry-leading bioinformatics pipeline, optimized over the course of more than a decade by leveraging manufacturing and assay performance data. TaqMan Assays have been cited in over 40,000 publications and are backed by more than 350 patents.
Recommended master mix (sold separately): TaqMan Genotyping Master Mix (Cat. No. 4371355)

Especificaciones
40X | |
7500 System, 7500 Fast System, 7900HT System, StepOne™, StepOnePlus™, ViiA™ 7 System, QuantStudio™ Absolute Q Digital PCR System, QuantStudio™ 3, QuantStudio™ 5, QuantStudio™ 6 Flex, QuantStudio™ 7 Flex, QuantStudio 6 Pro, QuantStudio 7 Pro, QuantStudio™ 12k Flex ProFlex PCR System*, VeritiPro*, SimpliAmp*, MiniAmp*, Automated Thermal Cycler** If a thermal cycler is used for PCR amplification, the optional pre-read and the post-read must be performed separately on a real-time PCR system in order to detect and record fluorescent signals. | |
5000 (placa de 384 pocillos); 1000 (placa de 96 pocillos) | |
Ensayos TaqMan personalizados | |
Temperatura ambiente |
1 tubo que contiene una mezcla de 40x (tamaños S y M) u 80x (tamaño L) de ensayo preformulado (2 sondas y 2 cebadores). Almacenar a entre -15 y -25 °C. |
|
Embalaje sostenible | |
TaqMan™ | |
M (1000 reactions), made to order | |
No humano |
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Para uso exclusivo en investigación. No apto para uso en procedimientos diagnósticos.