IDT termékek szállítási költségei 2024.04.-től:
A szintézis helyétől, valamint a szállítási körülményektől függően az alábbi költségek kerülnek felszámításra:
Általános tájékoztató az IDT USA gyártási központjából érkező „custom” termékcsoportokról:
szintetikus biológiai termékek:
qPCR próbák:
a szintézis helye a szekvencia komplexitásától, valamint a választott festék/ quencher kombinációtól függ
szolgáltatások:
stock termékek:
nem áll teljes lista rendelkezésre, kérjen ajánlatot a Bio-Science Kft.-től!
xGen Custom Amplicon Panels are custom-designed primer pools to create multiple overlapping amplicons for specific genetic targets in research studies (Figure 1). Panels can multiplex hundreds to thousands of targets in a single tube using a simple 2-hour workflow (Figure 2). Compatible with cell-free DNA and FFPE (formalin-fixed paraffin embedded) research samples starting with as little as 10 ng input or pathogen RNA/DNA in the picogram range. For a listing of the specifications for custom panels, see Table 1. If multiple libraries are being examined at the same time, the final NGS library can be normalized using the IDT proprietary xGen Normalase reagent.
The cost-effective and flexible custom design means the panel can be used for research applications such as:
Figure 1. xGen Custom Amplicon Panels are used to create targeted NGS libraries for research studies. Whether you need to examine hundreds or thousands of targets, the xGen Custom Amplicon Panels can be tailored to your specific research needs. Once created, the panel is used in a simple, one-tube workflow that is compatible with high-throughput applications.
Table 1. Product specifications of the xGen Custom Amplicon Panels
Feature | Specification |
---|---|
Input DNA range | 10–25 ng of amplifiable DNA |
Amplicon size | Versatile size for compatibility with many research sample types: whole blood, cell culture, FFPE, cfDNA (default maximum is 150 bp) |
Custom design coverage | >90% of requested bases |
Workflow time | Single-tube with 2-hour DNA-to-library workflow |
Components provided | Custom primer pool |
Limit of detection | As low as 1% allele frequency for variants |
Panel size range | 15–1500 amplicons per panel; other options available upon request |
Library multiplexing capability | Depends on type of indexing primers used |
On-target % | >90% on-target reads |
Coverage uniformity | >80% coverage uniformity at a >0.2 of mean depth |
Compatible platforms | Illumina®, Ion Torrent® |
From DNA to NGS library in as little as 2 hours, the workflow for the xGen Custom Amplicon Panels can be done in a single tube with minimal hands-on steps. As shown in Figure 2, the DNA sample is first amplified with the multiplex custom panel to create copies of each of your intended targets. Then the amplicons are converted into indexed libraries in a second PCR reaction with the appropriate indexing primers for your NGS instrument. When multiple libraries are pooled, IDT-proprietary xGen Normalase reagent is used to normalize the libraries for NGS analysis.
Figure 2. xGen Custom Amplicon Panels have a single tube workflow that is done in as little as 2 hours. Creating an NGS library starts with multiplex PCR. Your custom panel is combined with the DNA sample to amplify the targets of interest. The samples are then amplified with indexing primers to create a functional dual indexed library. As an optional step, the xGen Normalase reagent can be used after pooling multiple libraries to ensure each is equally represented in the final sample for the flowcell.
For research use only. Not for use in diagnostic procedures. Unless otherwise agreed to in writing, IDT does not intend for these products to be used in clinical applications and does not warrant their fitness or suitability for any clinical diagnostic use. Purchaser is solely responsible for all decisions regarding the use of these products and any associated regulatory or legal obligations.
This technology enables design of custom panels for targeted sequencing, offering a completely curated, targeted NGS workflow to rapidly interrogate genomic targets relevant to your research.
This technology enables low-frequency variant identification ≤1% through the incorporation of molecular identifiers (MIDs or UMIs), to promote improved sensitivity and specificity by removing false positive errors introduced during PCR and sequencing.
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