SYNTOL / SOLUTION

GMO analysis

From screening to event identification and quantitative analysis

SYNTOL solutions for GMO analysis cover DNA extraction from plant, food, raw-material, feed, and seed matrices, screening of regulatory sequences, identification of transformation events, and quantitative analysis where supported by the specific assay.

For laboratories testing food, raw materials, feed, and seeds

The page helps laboratories choose the next analytical step: prepare DNA, perform screening, confirm a transformation event, or carry out quantitative analysis. The regulatory status of an event is treated separately and must always be tied to a date and jurisdiction.

LABORATORY PROBLEM

Laboratory tasks

  • extract DNA from plant material, food/raw materials, feed, or seeds;
  • automate DNA extraction for documented sample types;
  • confirm suitable plant DNA or an endogenous target;
  • screen 35S, FMV, NOS, SsuAra/E9, nptII, and other supported targets;
  • proceed from a positive screen to identification of a specific event or group of events;
  • perform semiquantitative or quantitative analysis only when included in the assay's intended use;
  • verify instrument compatibility and access current documentation.
SCIENTIFIC ROUTE PLATE

Analytical sequence

Presentation schematic / not to scale
Primary laboratory route
01

DNA extraction

Depending on the matrix, use Sorb-GMO-A, Sorb-GMO-B, or automated Sorb-GMO-B-Automatic.

02

Screening

Determine plant/endogenous targets and regulatory sequences covered by the chosen kit.

03

Identification

Where required, use real-time PCR for a specific transformation event or multiple events.

Conditional analytical path
A

Quantitative analysis

Show only active assays whose intended use includes quantitative determination.

The GMO Detect portfolio

The portfolio includes manual and automated DNA extraction, screening assays, event-specific and multi-event identification, and products for quantitative analysis. Supporting plant-identification assays help assess sample suitability and guide the next analytical step.

Methods

The principal methods are DNA extraction, automated magnetic extraction, and real-time PCR. Screening, event identification, and quantitative analysis are distinct analytical tasks built on the same methodological foundation.

Products and assays

Products for key stages

Key sample-preparation products include Sorb-GMO-A, Sorb-GMO-B, and Sorb-GMO-B-Automatic. GM-415 Plant/35S+FMV/NOS Screening can illustrate the screening stage. The current range of event-identification and quantitative-analysis assays is available in the catalog and updates with the product line.

01 Shown now 12
02 Public range 107
03 Presentation Representative selection
04 Application groups 4
05 Workflow stages 1
Show current assortment107
RESOURCES AND ACTIONS

Move from the task to concrete resources

Methodological materials2
Knowledge material

“Sorb-GMO-A” and “Sorb-GMO-B” – reagent kits for DNA extraction from food products, plant raw material and feed

Open material
Services1

User Training

Practical user training for working with reagents, protocols and laboratory scenarios.

Open service
Important considerations

Regulatory context and limitations

The regulatory status of a transformation event is stated only with a date and jurisdiction. Sensitivity, specificity, turnaround, and semiquantitative thresholds belong to the specific assay; obsolete portfolio-coverage figures are not used.

NEXT STEP

Select an analytical scheme

Primary action: “Select a GMO analysis scheme.” Choose screening, event identification, quantitative analysis, DNA extraction, or automation. Additional actions: “Check compatibility” and “Request training.”

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What do you need to do?

Describe the laboratory task in normal language. I will use the appropriate verified SYNTOL tool.

Critical procedures remain grounded in approved product data and references.