Nucleic Acid Isolation Kit

The MagMAX Viral/Pathogen Nucleic Acid Isolation Kit is designed to recover RNA and DNA from virus and gram-negative bacteria in samples such as blood, swabs, urine, and viral transport media (VTM). The kit utilizes MagMAX magnetic-bead technology, ensuring reproducible recovery of high-quality nucleic acid compatible with a broad range of applications, including real-time PCR, digital PCR, and next-generation sequencing.

Features of the MagMAX Viral/Pathogen Nucleic Acid Isolation Kit include:
Automation-ready protocols designed for the KingFisher Flex and KingFisher Duo Prime systems
Fast procedure allows for 96 samples to be processed in <30 minutes
Flexible protocol accommodates sample volume inputs from 200 µL to 2 mL of biofluids or transfer media
No need for carrier RNA
Elution volumes ranging from 50 to 100 µL

The Nucleic Acid Isolation Kit (Magnetic Beads Method) is designed for the automated purification of RNA and DNA from body fluids (such as swabs, plasma, serum) using automated nucleic acid extraction instruments. Magnetic- particle technology provides high-quality DNA/RNA that is suitable for direct use in downstream applications such as amplification or other enzymatic reactions.
We provide different models to match different machines, also, we can provide OEM service for customers

This product makes use of the specific binding capacity of superparamagnetic beads for
high-throughput purification of high-quality DNA/RNA from a variety of sample types including:
fresh or frozen animal tissue, blood, cells, saliva, mouthwash, mammalian cell cultures and
nasal/throat swabs. The components of this kit are specially optimized for rapid automatic
extraction and are recommended for extraction with automatic instruments.

Features:
Fast 6.5 minutes procedure yields pure, integrated length DNA/RNA
Versatile High linearity from 10 to 10 copies of pseudovirus.
Sensitive The extraction limit is as low as 10 copies (Ct38).
Robust Sample size from 100 L to 40 L showed good performance.

Magnetic bead-based purification 1. High-quality nucleic acid can be obtained range from 10 min to 40min (up to different protocol). 2. High throughput: Can be integrated with magnetic rod method automatic instrument or pipetting method automatic instrument to carry out high throughput extraction experiment. 3.Safe and nontoxic: No toxic organic reagents such as phenol/chloroform are needed. 4.Complete removal of contaminants and PCR inhibitors for downstream experiments.

CE Magnetic Bead Method Nucleic Acid Extraction and Purification Kit

It's designed for the rapid, efficient and automatic isolation and purification of high quality virus nucleic acid from a variety of samples on the automatic nucleic acid extraction system.

Features:
1): Rapid and Reliable: Fast procedures and easy to use
2): High Sensitivity
3): High Efficiency: â?¥ 95% of the nucleic acid can be combined.
4): Versatile: Nucleic acid of various virus, Hepatitis, etc. in different samples, such as Serum, Plasma, Whole blood, Swabs, Saliva, Body fluid, Tissue, Feces, BALF, etc. for a broad range of down stream applications.
5): Safe: Non-toxic

Certification - Test Report/CE

Daily manufacturer output - TBD

Price - $25
Volume dependent

Real-time PCR test
96 Reactions/kit

ExProbeTM SARS-CoV-2 qPCR Testing Kit
EU CE Marked,
US FDA EUA Approved,
Taiwan FDA EUA Approved
Intended Use: To detect RdRP/N/E RNA SARS-CoV-2 (COVID-19) in NP/O swabs and sputum. 
Product Format: 96 tests/kit
Kit Contents: PCR Mix, Enzyme Mix, Pos. Control, Neg. Control and Instruction For Use.
Storage / Stability: -20C + 5C / 6 months, repeat freeze thaw x 4.
Testing kit is compatible for ABI7500,Roche 4800, TBG Q6000 qPCR Systems
Reproducibility / Precision 100% Concordant across 3 lots with CV + 5%
Limits of Detection (LOD) 50 copies/reaction
Performance Comparison* Positive Samples 5 / 5 Negative Samples 199/200

[Intended Usage]
This kit is used for the in vitro qualitative detection of suspected cases of pneumonia caused by New Coronavirus infection, patients with suspected clusters, other patients who need to be diagnosed or differentially diagnosed with the New Coronavirus infection, and nasopharyngeal swabs, oropharyngeal swabs, and bronchoalveolar lavage fluid samples of patients with mutation beads for the New Coronavirus ORF1ab and N gene, S gene N501Y mutation and S gene E484K mutation sites.

[Storage Conditions & Validity]
1. The kit should be stored frozen at -20 and protected from light; the expiration date is 6 months; the production date and expiration date are shown in the outer packaging box.
2. Avoid repeated freezing and thawing of the kit and the number of freezing and thawing shall not exceed 7 times.
3. After opening, the bottles should be stored at -20 and protected from light. The number of bottles opening times should not exceed 7 times, which will not affect the use within the validity period.

[Applicable Instruments]
1. This kit has been validated on ABI7500 quantitative fluorescence PCR instrument.
2. For other models not listed, relevant experiments have not been performed or completed for this kit. If users need to use this type of instrument platform to carry out the detection of this reagent, please contact our Technical Department at for relevant support.
NB: The other devices can include quantitative fluorescence PCR platforms with FAM, VIC, ROX and Cy5 channels.

[Sample Requirements]
1. Nasopharyngeal swabs, oropharyngeal swabs and other methods are used to obtain samples, and it is recommended to use commercial virus sampling kits for sample collection devices.

[Test Results Interpretation]
1. Negative and positive controls should be tested in each experiment and the test result can be determined only when the controls meet the quality control requirements.
2. When FAM, VIC and ROX channels are positive, Cy5 channel result may be negative due to the system competition.
3. When the internal standard result is negative, if the FAM, VIC and ROX signals of the test sample are also negative, the test result of the sample is invalid, and the cause should be found and eliminated, and the experiment repeated for this sample.

[Product Performance Index]
1. Precision: The coefficient of variation Intra-batch / Inter-batch, Intra-day / Inter-day among different operators shall not be higher than 5.0%.
2. Coincidence rate of negative positive controls: The coincidence rate of positive controls and negative controls is 100%.
3. Minimum detection limit: The minimum detection limit of this kit is 500 copies/mL.

[CE Mark Registration No.]: RPS/499/2021.
[EC REP.]: CMC MEDICAL DEVICES & DRUGS S.L. C/ Horacio Lengo n18, C.P 29006, Milaga, Spain.