Archer VARIANTPlex BRCA v3 Panel
Vendor: Archer
SKU: AB0233
In stock
Discover important alterations for inherited disease research
Screen samples for BRCA mutations with targeted NGS. Identify SNVs, indels, and large intragenic copy number variants.
Key Benefits
- Integrated Solution — Anchored Multiplex PCR (AMP™) chemistry paired with purpose build analysis software enables you to detect complex variants on a single solutions platform.
- 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.
- Scale easily — Liquid reagents enable automated liquid handling workflows for high volume research labs, while Anchored Multiplex PCR (AMP™) chemistry fuels reliable performance at scale.
Panel Specifications
| Targeted genes | 2 |
| Genomic alterations | SNV, indels, intragenic CNVs |
| Input nucleic acid required* | ≥10 ng |
| Recommended number of reads | 200,000 for germline applications 1 M for somatic applications |
| Hands-on time | <2.5 hours |
| Total library prep time | 1.5 days |
| Platform compatibility | Illumina® |
| Reagent format | Lyophilized or liquid |
| Supported sample types | Whole blood, saliva, FFPE |
* 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
BRCA1, BRCA2
Documents
User guides and protocols
- VARIANTPlex-LAC Protocol for Illumina (PDF)
- VARIANTPlex-HT Protocol for Illumina (PDF)
- VARIANTPlex Protocol for Illumina (PDF)
- VARIANTPlex HS-HGC Protocol for Illumina (PDF)
Product inserts
Ordering Information
| Cat. # | Kit | Format |
|---|---|---|
| AB0233 | VARIANTPlex-HGC 2.0 BRCA v3 ILMN 8rxn | HGC 2.0 / Illumina / 8 rxn |
| AB0235 | VARIANTPlex-LAC BRCA v3 ILMN 8rxn | LAC / Illumina / 8 rxn |
| AB0237 | VARIANTPlex-HT BRCA v3 ILMN 24rxn | HT / Illumina / 24 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 2 genes
- Hands on time <2.5 hours
- Input quantity ≥10 ng
- Platform compatibility Illumina
- Reagent type Lyophilized or liquid
- Specialized sample types Whole blood, saliva, FFPE
- Sub category VARIANTPlex
- Variant class SNV, indels, intragenic CNVs
links and documants
- Datasheet url Click here
- Protocol url Click here
- Source url Click here
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Archer VARIANTPlex BRCA v3 Panel
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