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Description
Includes
SNaPshot™ Multiplex Ready Reaction Mix (for 100 reactions), SNaPshot™ Multiplex Control Primer Mix (30μL), SNaPshot™ Multiplex Control Template (60μL)
- Interrogate up to 10 SNPs from different amplicons in a single base extension reaction
- Separate SNP loci that differ by a single base pair
- Increased sensitivity compared to standard sequencing allows detection of minor variants (e.g. somatic mutations) in a test sample
- Reduce the complexity of your experiments with this easy to use and cost-efficient genotyping system
- A large body of scientific literature demonstrates the utility for genotyping, mutation detection and mapping
Order Info
Each
Specifications
Specifications
| Content And Storage | Contains: • SNaPshot™ Multiplex Ready Reaction Mix (for 100 reactions) • SNaPshot™ Multiplex Control Primer Mix (30 μl) • SNaPshot™ Multiplex Control Template (60 μl) Store at -15°C to -25°C in a constant-temperature freezer. |
| Description | SNaPshot™ Multiplex Kit, 100 rxns, Capillary Electrophoresis Detection Method, DNA Sample Type, AmpliTaq™ DNA Polymerase, SNPs (Known) Genotyping Target, Multiplexing High Throughput Compatibility, Unlabelled Oligos Primer-Probe Compatibility |
| Detection Method | Primer-probe |
| Format | Tube |
| Polymerase | AmpliTaq DNA Polymerase |
| Reaction Speed | 8 hr. |
| Technique | SNP Genotyping (Fragment Analysis-Based), Primer Extension |
| For Use With (Equipment) | 3500 Series Genetic Analyzers, SeqStudio Flex Series Genetic Analyzers, SeqStudio Genetic Analyzer, 3730/3730xl Genetic Analyzers |
| High-throughput Compatibility | Multiplexing |
| Product Line | SNaPshot |
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Frequently Asked Questions (FAQs)
The SNaPshot Multiplex Kis is designed to interrogate up to 10 single nucleotide polymorphisms (SNPs) at known locations on 1-10 templates in a single tube.
The extra peaks could be due to incomplete removal of PCR primers, incomplete removal of dNTPs from the PCR reaction, or incomplete removal of the fluorescently labeled ddNTPS from the SNaPshot reaction. Residual PCR primers and dNTPs will both participate in the SNaPshot reaction. For the PCR purification, please use fresh SAP and Exo1 or use another method of PCR purification. To address incomplete removal of fluorescently labeled ddNTPS, use fresh CIP or SAP.
Due to the influence of the dye on the mobility shift of the DNA fragments, the reported sizes will differ by a few bases from the actual sizes. This is particularly true with the shorter fragments as the relative contribution of the dye is greater. It is also recommended that you have a tail on the primer with a 5-7 bp difference between them to further separate the samples so there is no overlap.
This is normal as the SNaPshot control shown in the manual is from a 3100 Genetic Analyzer and POP-4 polymer. Dye-labeled DNA fragments can yield different sizes when run with a different instrument, polymer type, capillary array length, or size standard. Although the control sizes may not match that in the protocol, once the size has been established, the precision, or reproducibility will be consistent for a given fragment.
For Research Use Only. Not for use in diagnostic procedures.
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