Mimix™ Non-Small Cell Lung Cancer Panel ctDNA Negative Control Reference Standard
The Non-Small Cell Lung Cancer ctDNA Panel reference standard negative control is thoroughly tested and confirmed to be negative for all the 22 clinically relevant mutations using ddPCR. This cell line-derived panel is manufactured under ISO 9001:2015 and ISO 13485:2016. This panel can be used as a negative control or to dilute the allele frequency of the NSCLC ctDNA panel reference standard - HD844 further enabling validation of MRD.
Technical data
Format: ctDNA
Genes covered: EGFR, KRAS, BRAF, MET, ERBB2, PIK3CA, NRAS
Allelic frequencies: 0.00%
Buffer: Tris-EDTA (10mM Tris-HCl, 1mM EDTA), pH 8.0
Product information
Fragment size: 160 bp
Unit size: 350 ng per vial
Concentration: 20 ng/µL
Verified mutations:
| Gene | DNA sequence change | Amino acid change | Expected allelic frequency (%) |
|---|---|---|---|
| BRAF | c.1799T>A | p.V600E< | 0.00 |
| EGFR | c.2156G>C | p.G719A | 0.00 |
| EGFR | c.2303G>T | p.S768I | 0.00 |
| EGFR | c.2582T>A | p.L861Q | 0.00 |
| EGFR | c.2573T>G | p.L858R | 0.00 |
| EGFR | c.2235_2249del | p.E746_A750del | 0.00 |
| EGFR | c.2236_2250del | p.E746_A750del | 0.00 |
| EGFR | c.2240_2257del | p.L747_P753delinsS | 0.00 |
| EGFR | c.2369C>T | p.T790M | 0.00 |
| ERBB2 | N/A | Amplification | 2 copies |
| ERBB2 | c.2313_2324dup | p.Y772_A775dup | 0.00 |
| ERBB2 | c.2331_2339dup | p.G778_P780dup | 0.00 |
| KRAS | c.34G>T | p.G12C | 0.00 |
| KRAS | c.35G>T | p.G12V | 0.00 |
| KRAS | c.35G>A | p.G12D | 0.00 |
| MET | N/A | Amplification | 2 copies |
| MET | c.3802+1G>T | Unknown (Exon 14 skipping) | 0.00 |
| NRAS | c.181C>A | p.Q61K | 0.00 |
| NRAS | c.182A>T | p.Q61L | 0.00 |
| NRAS | c.182A>G | p.Q61R | 0.00 |
| PIK3CA | c.1624G>A | p.E542K | 0.00 |
| PIK3CA | c.3140A>G | p.H1047R | 0.00 |
General information
Storage: 4°C
Expiration: See all product shelf life information
Quality control
Fragmentation size: D1000 DNA ScreenTape assay
Allelic frequency: Droplet Digital™ PCR
Quantification: Qubit® dsDNA BR assay (Invitrogen)
Intended use: For assay developers and molecular diagnostic labs for routine performance monitoring of molecular biology assays. Research use only. Not for diagnostic procedures.
References
- Kris MG, Camidge DR, Giaccone G, et al. Targeting HER2 aberrations as actionable drivers in lung cancers: phase II trial of the pan-HER tyrosine kinase inhibitor dacomitinib in patients with HER2-mutant or amplified tumors. Ann Oncol. 2015;26(7):1421-1427. doi:10.1093/annonc/mdv186
We accept orders using the following methods.
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Our online catalog and ordering system can be used to search our full menu of available Reference Standards. Select your desired reference standards and add them to the shopping basket. Your order can be submitted instantly using credit card, telephone ordering or a purchase order number as the preferred payment method.
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If you prefer to send us orders outside our online ordering system, please see the Contact Us page for telephone, fax, and email details in order to place an order. We recommend that you use our online system to identify the products you require and their respective “HD” product codes.
To order offline we will require the following information:
- Product code(s) of the item(s) you wish to order (e.g. "HD123")
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Reference Standards
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At what temperature do you ship reference standards?
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How are Horizon cfDNA and ctDNA Reference Standards different from other circulating tumor DNA controls?
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How are Horizon cfDNA and ctDNA Reference Standards fragmented?
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How do you manufacture your Horizon Reference Standards?
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Is it possible to order custom versions of Horizon Reference Standard?
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Is there a wild-type control in the same background as NSCLC ctDNA Panel Reference Standard (HD844)?
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What are cfDNA Reference Standards?
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What is MRD?
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What is the difference between ctDNA and cfDNA?
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Which Droplet Digital PCR (ddPCR) system is used for variant detection at Horizon?
Related Products
Improve your MRD assay validations using our new Non-Small Cell Lung Cancer ctDNA Reference Standard. It is a well characterized, cell line-derived control material manufactured under ISO 9001:2015 and ISO 13485:2016 that contains 22 clinically relevant variants across 7 genes.