BIFOUR Biotech · Nucleic-acid preparation
NAE 2
A compact solution for standardising nucleic-acid extraction before amplification. Automated preparation reduces the effect of manual handling on PCR reproducibility.
Quick decision
Is this test right for your control programme?
Consider it when
Laboratories building a connected sample-to-result workflow
We clarify before quoting
Matrix and sampling point, target, decision threshold, test volume, compatible reader, control points, frequency and approved procedure.
Another test may be better when
The matrix, analytical target, required limit, time to result, readout format or approved procedure differs.
Best suited for
Laboratories building a connected sample-to-result workflow
Capabilities and controlled parameters
- Automation of repetitive sample-preparation steps
- Reduced operator-to-operator variability
- Designed to support a connected workflow with PCR instruments and compatible assays
- Protocols and consumables must be selected for the specific sample type
LabLog
Implementation considerations
Test implementation starts with the matrix, sampling point, analytical target and decision rule. Before supply, LabLog checks reader and consumable compatibility, control requirements, frequency, training, storage and result documentation.
How LabLog supports the project
- 01Define the matrix, sampling point and target
- 02Check the decision threshold and applicable method
- 03Agree the reader, tests, controls and stock level
- 04Prepare storage, training and a working instruction
- 05Verify a trial cycle before routine use