AmpliSeq for Illumina Myeloid Panel
Vendor: Illumina
SKU: 20024478
In stock
Fixed panel includes 74 genes associated with hematologic malignancies. Kit contains 24 reactions (24 DNA libraries and 24 RNA libraries). Requires 48 reactions of LP PLUS. Library PLUS, indexes and cDNA synthesis sold separately.
The Myeloid Panel enables concurrent analysis of both DNA and RNA from blood and bone marrow samples in a single assay to study biomarkers associated with hematologic malignancies. The panel covers relevant targets for these major myeloid disorders: acute myeloid leukemia (AML), myeloid dysplastic syndrome (MDS), myeloproliferative neoplasms (MPN), chronic myeloid leukemia (CML), chronic myelomonocytic leukemia (CMML), and juvenile myelomonocytic leukemia (JMML). Key features include:
Documents
- Automated Solutions for AmpliSeq for Illumina Sequencing Panels
- AmpliSeq for Illumina Myeloid Panel Data Sheet
Support Documentation
- AmpliSeq for Illumina Myeloid Panel Checklist Documentation
- Illumina Adapter Sequences Documentation
- AmpliSeq for Illumina Myeloid Panel Documentation
- Index Adapters Pooling Guide Documentation
- AmpliSeq for Illumina Myeloid Panel Reference Guide Documentation
- AmpliSeq for Illumina Myeloid Panel Consumables & Equipment Documentation
- All AmpliSeq for Illumina Myeloid Panel Support
Specifications
- Area of interest Cancer research
- Assay time 5.5 – 7.5 hours (library prep only; doesn't include library quantification, normalization, or pooling time)
- Cancer type Hematologic
- Content specifications Targets biomarkers across 69 genes (40 key DNA target genes, 29 RNA fusion driver genes, and 5 gene expression levels)
- Hands on time < 1.5 hr
- Input quantity 20 ng high-quality DNA; 10 ng high-quality RNA (10 ng recommended per pool)
- Instruments MiSeq SystemMiniSeq System
- Key use Targeted analysis
- Method Amplicon sequencing, Targeted DNA sequencing, Targeted RNA sequencing
- Multiplexing Up to 96-plex
- Nucleic acid type DNA, RNA
- Specialized sample types Blood, Bone marrow, Not FFPE-compatible
- Species category Human
- Sub category Library preparation kits
- Technology Sequencing
- Variant class Gene fusions, Insertions-deletions (indels), Single nucleotide polymorphisms (SNPs), Somatic variants
links and documants
- Datasheet url Click here
- Source url Click here
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AmpliSeq for Illumina Myeloid Panel
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