EGFR-Multiplex Set cfDNA in Plasma

EGFR mutations are driver mutations, they are common and cause lung and breast cancer. The mutations of the SensID EGFR-Multiplex product consist of a selection of TKI sensitive and TKI resistant mutations, which are relevant for the therapy of the Non-Small Cell Lung Cancer.

The EGFR-Multiplex Set cfDNA in plasma product can be used in diagnostics as a positive standard in liquid biopsy assays in your laboratory or R&D department, as well as for validation and development of EGFR diagnostic kits. The background material is human cfDNA of the Ashkenazim Son cell line, as well as human-tech plasma (human recreated).

SKU: SID-000020 Category:

Product description

Tailored to your needs: From bulk delivery and custom batch sizes to self-crafted with the corresponding cfDNA in buffer product!

OEM options:

If you need materials as in kit controls or as a third party control for validation of your kits at customer labs, please contact us via: sales@sens-id.com

Self-Crafted Solution:

How to create your full workflow plasma control material:

If you prefer to make your own full workflow controls we recommend using our DNA depleted plasma products. Blend the DNA as necessary with the DNA depleted plasma to receive plasma materials with the necessary DNA concentrations.

This product as cfDNA in buffer can be found here:

Combine with:

And create your own plasma materials.

These products are ideal for digital PCR and/or Next Generation Sequencing (NGS). In particular:
– Validation and development of sequencing protocols (e.g. Whole Genome Sequencing (WGS), Amplicon Sequencing) and PCR protocols
– Determination of the detectiont limit of the method
– to control the extraction efficiency

Fragmentation Size (peak)
~167 bp

Unit Size: as desired

Mutation:

AA Change (Cosmic ID, mutation type, HGVS nomenclature, Exon)

  • p.G719S (COSV51767289*, Substitution, c.2155G>A, Exon 18)
  • p.E746_A750delELREA (COSV51765066*, Deletion, c.2236_2250del15, Exon 19)
  • p.S752_I759delSPANKEI (COSV51774879*, Deletion, c.2254_2277del24, Exon 19)
  • p.S768I (COSV51768106*, Substitution, c.2303G>T, Exon 20)
  • p.V769_D770insASV (COSV51850427*, Insertion, c.2303_2304ins9, Exon 20)
  • p.T790M (COSV51765492*, Substitution, c.2369C>T, Exon  20)
  • p.L858R (COSV51765161*, Substitution, c.2573T>G, Exon 21)
  • p.L861Q (COSV51766344 *, Substitution, c.2582T>A, Exon 21)

Allele frequencies: 0%, 0.1%, 1%, 5%

Buffer: Plasma (human-tech)

Storage: 2-8 °C

Expiry:
Stable up to 24 months after date of manufacture (as supplied). In the case of in-house production, this depends on the manufacturing conditions

Quality control

Fragmentation size: High Sensitivity DNA Kit Agilent

Allele Frequency: dPCR

Quantification:

  • UV-Vis Spectrophotometry (NIST-Reference method)
  • dsDNA (fluorometric measurement)

Technical background

Derived from: cell line GM24385 (HG002- NA24385 – huAA53E0)

Bioinformatics:
– lot specific sequencing files: LOT Search
– High-confidence variant calls: ftp://ftp-trace.ncbi.nlm.nih.gov/giab/ftp/release/AshkenazimTrio
– Raw datasets and bam files, currently including 10X Genomics, BioNano, Complete Genomics regular and LFR, 300x Illumina paired-end, Illumina 6kb mate-pair, 1000x Ion exome, custom moleculo libraries, ~0.05x Oxford Nanopore, and 70x/30x/30x PacBio: ftp://ftp-trace.ncbi.nlm.nih.gov/giab/ftp/data/AshkenazimTrio/HG002_NA24385_son/

*GRCh 38 Cosmic v88

Documents

Certificate of Analysis:

                            
–> 0%                                             –> 0.1%                                        –> 1%                                         –> 5%

   Lot: 00025                             Lot: 00036                                  Lot: 00028                             Lot: 00035

other Documents:

Instructions for use

Safety Data Sheet (SDS ​​available on request. Please contact the support.)

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