Archer VARIANTPlex Core Solid Tumor Panel
Vendor: Archer
SKU: AB0140
In stock
Identify DNA profiles of multiple cancers with one core panel
Efficiently detect single nucleotide variants, insertions and deletions, copy number variations, and microsatellite instability with targeted NGS of 60 genes relevant for colorectal, breast, melanoma, pancreatic, NSCLC, and other cancer research.
Key Benefits
- Detect confidently — A unique outlier detection algorithm leverages position-specific data to enable variant detection even at low allele frequencies, one of the many ways that Archer Analysis empowers you to detect confidently.
- Less QNS — Anchored Multiplex PCR (AMP™) chemistry is designed for compatibility with a wide range of sample types, including low-input and potentially degraded samples such as FFPE tissue.
- Achieve efficiency — Streamlined workflows for your lab are enabled by choice of reaction-sized lyophilized reagents or high-throughput liquid reagents, while parallel workflows across all Archer panels provide efficient genomic characterization.
- Customize content — Use Assay Marketplace to modify any panel to fit your lab's needs or start from scratch to keep up with the pace of discovery.
Panel Specifications
| Targeted genes | 60 |
| Genomic alterations | SNVs, indels, CNVs, ITDs, MSI |
| Input nucleic acid required* | ≥10 ng |
| Recommended number of reads | 4.5 M |
| Hands-on time | <3.5 hours |
| Total library prep time | 1.5 days |
| Platform compatibility | Illumina® |
| Reagent format | Lyophilized or liquid |
| Supported sample types | FFPE, fresh frozen, cytology smear, FNA |
*Input mass requirements vary depending on type and quality. Unless the tumor cellularity and sample quality are high, 50 ng of FFPE-derived nucleic acid should be considered the minimum recommendation. If input is not limiting, 200 ng is recommended.
Gene Targets
AKT1, BRAF, EGFR, ERBB2, FOXL2, GNA11, GNAQ, GNAS, HRAS, IDH1, IDH2, KIT, KRAS, MET, NRAS, PDGFRA, PIK3CA, RET, TERT, TP53, ALK, APC, AR, ATRX, CDK4, CDK6, CDKN2A, CTNNB1, DDR2, ERBB3, ERBB4, ESR1, FBXW7, FGFR1, FGFR2, FGFR3, H3F3A, HIST1H3B, JAK2, MAP2K1, MAP2K2, MTOR, MYC, NOTCH1, NOTCH2, NOTCH3, NOTCH4, NTRK1, NTRK2, NTRK3, POLD1, POLE, PTEN, RAF1, RB1, RICTOR, ROS1, SMAD4, SMO, VHL
Documents
User guides and protocols
Product inserts
- VARIANTPlex-HT Core Solid Tumor Panel Product Insert (PDF)
- VARIANTPlex Core Solid Tumor Product Insert (PDF)
Ordering Information
| Cat. # | Kit | Format |
|---|---|---|
| AB0140 | VARIANTPlex-HGC 2.0 Core Solid Tumor ILMN 8rxn | HGC 2.0 / Illumina / 8 rxn |
| AB0171 | VARIANTPlex-HT Core Solid Tumor ILMN 24rxn | HT / Illumina / 24 rxn |
| AB0172 | VARIANTPlex-HT Core Solid Tumor ILMN 96rxn | HT / Illumina / 96 rxn |
HT kits are liquid reagents for high-throughput / automated workflows (Illumina only). For research use only. Not for use in diagnostic procedures.
Specifications
- Assay time 1.5 days
- Content specifications 60 genes
- Hands on time <3.5 hours
- Input quantity ≥10 ng
- Platform compatibility Illumina
- Reagent type Lyophilized or liquid
- Specialized sample types FFPE, fresh frozen, cytology smear, FNA
- Sub category VARIANTPlex
- Variant class SNVs, indels, CNVs, ITDs, MSI
links and documants
- Datasheet url Click here
- Protocol url Click here
- Source url Click here
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Archer VARIANTPlex Core Solid Tumor Panel
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