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Citations & References (7)
Applied Biosystems™
MagMAX™ Prime Viral/Pathogen NA Isolation Kit
The MagMAX Prime Viral/Pathogen NA Isolation Kit is a magnetic-bead-based nucleic acid purification kit for the isolation and purification ofRead more
| Catalog Number | Quantity |
|---|---|
| A58145 | Up to 600 reactions |
Catalog number A58145
Price (CLP)
1.381.124
Each
Quantity:
Up to 600 reactions
Price (CLP)
1.381.124
Each
The MagMAX Prime Viral/Pathogen NA Isolation Kit is a magnetic-bead-based nucleic acid purification kit for the isolation and purification of viral, bacterial, parasitic, and fungal nucleic acid from human biological specimens.
Features of the MagMAX Prime Viral/Pathogen NA Isolation Kit include:
• Designed to isolate and purify microbial nucleic acid from a range of biological samples such as swabs in transport media, saliva, stool, urine, plasma, and serum
• Flexible workflow allowing various sample types to be batched on a single plate
• Streamlined automation-ready protocols designed for basic and advanced lysis and advanced stool workflows
• Fast automated KingFisher Flex, KingFisher Apex, KingFisher Apex Dx (RUO mode) scripts to allow for 96 samples to be processed in less than 60 minutes
• Flexible protocol accommodates sample volume inputs of 200–400 μL
• Elution volume of 200 μL for stool samples and 60 μL for all other sample types
• Available lysis buffers and bead-beating accessories to extract nucleic acids from challenging organisms and raw/stabilized stool sample type
The kit is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in automated magnetic bead purification techniques.
Compatible with Thermo Fisher infectious disease research assays
Have confidence that your nucleic acid extraction kit will work with your downstream application and enjoy a complete solution from Thermo Fisher Scientific.
Benefits of MagMAX magnetic bead–based purification
Magnetic beads offer many benefits compared to other technologies for isolating nucleic acid. Beads bind the nucleic acid more efficiently than glass-fiber filters, resulting in higher and more consistent yields. Additionally, because filters and vacuum manifolds are not used, there is no risk of filter clogging due to cellular particulates in samples. This clogging issue is of particular concern with protein-rich, large-volume samples such as whole blood or plasma that are commonly used for viral testing.
Accessories available for advanced workflow
Advanced lysis workflow
MagMAX Prime G+ Bacterial and Fungal Lysis Buffer
Advanced stool workflow
MagMAX Prime Stool Lysis Buffer
MagMAX Prime Bead Beating Tubes
Standalone reagents
MagMAX Prime Viral/Pathogen Binding Beads
MagMAX Prime Viral/Pathogen Elution Buffer
MagMAX Prime Viral/Pathogen Wash I Solution
MagMAX Prime Viral/Pathogen Binding Solution
MagMAX Prime Viral/Pathogen Proteinase K
MagMAX Prime Viral/Pathogen Proteinase K Dye
Features of the MagMAX Prime Viral/Pathogen NA Isolation Kit include:
• Designed to isolate and purify microbial nucleic acid from a range of biological samples such as swabs in transport media, saliva, stool, urine, plasma, and serum
• Flexible workflow allowing various sample types to be batched on a single plate
• Streamlined automation-ready protocols designed for basic and advanced lysis and advanced stool workflows
• Fast automated KingFisher Flex, KingFisher Apex, KingFisher Apex Dx (RUO mode) scripts to allow for 96 samples to be processed in less than 60 minutes
• Flexible protocol accommodates sample volume inputs of 200–400 μL
• Elution volume of 200 μL for stool samples and 60 μL for all other sample types
• Available lysis buffers and bead-beating accessories to extract nucleic acids from challenging organisms and raw/stabilized stool sample type
The kit is intended for use by qualified and trained clinical laboratory personnel specifically instructed and trained in automated magnetic bead purification techniques.
Compatible with Thermo Fisher infectious disease research assays
Have confidence that your nucleic acid extraction kit will work with your downstream application and enjoy a complete solution from Thermo Fisher Scientific.
Benefits of MagMAX magnetic bead–based purification
Magnetic beads offer many benefits compared to other technologies for isolating nucleic acid. Beads bind the nucleic acid more efficiently than glass-fiber filters, resulting in higher and more consistent yields. Additionally, because filters and vacuum manifolds are not used, there is no risk of filter clogging due to cellular particulates in samples. This clogging issue is of particular concern with protein-rich, large-volume samples such as whole blood or plasma that are commonly used for viral testing.
Accessories available for advanced workflow
Advanced lysis workflow
MagMAX Prime G+ Bacterial and Fungal Lysis Buffer
Advanced stool workflow
MagMAX Prime Stool Lysis Buffer
MagMAX Prime Bead Beating Tubes
Standalone reagents
MagMAX Prime Viral/Pathogen Binding Beads
MagMAX Prime Viral/Pathogen Elution Buffer
MagMAX Prime Viral/Pathogen Wash I Solution
MagMAX Prime Viral/Pathogen Binding Solution
MagMAX Prime Viral/Pathogen Proteinase K
MagMAX Prime Viral/Pathogen Proteinase K Dye
For Research Use Only.
Specifications
Bead TypeMagnetic
ColorClear
For Use With (Application)Next-Generation Sequencing, RT-PCR (Endpoint), Real-Time PCR
High-throughput CompatibilityHigh-throughput Compatible, Automated Protocols
Key FunctionsIsolate and purify viral, bacterial, parasitic, and fungal nucleic acid
No. of ReactionsUp to 600 Reactions
Nucleic Acid TypeDNA/RNA
Product LineMagMAX
Product TypeReagent
QuantityUp to 600 reactions
Sample TypeSwabs in Transport Media, Saliva, Urine, Serum, Plasma
Sample Volume200–400 μL
Shelf Life2 Years
Shipping ConditionRoom Temperature
TargetViral, Bacterial, Parasitic, and Fungal Nucleic Acid
FormatKit
Isolation TechnologyBeads
Unit SizeEach
Contents & Storage
• 160 mL Binding Solution
• 300 mL Wash I Solution
• 6 mL Binding Beads
• 3 mL Proteinase K
• 36 mL Elution Buffer
• 30 μL Proteinase K dye
Store at 15–25°C.
Citations & References (7)
Citations & References
Abstract
Microbiota-derived short-chain fatty acids mediate Candida albicans gastrointestinal colonization resistance.
Journal:Cell host & microbe
PubMed ID:42242208
Streamlined CRISPR-based assays for detection and subtyping of avian influenza.
Journal:medRxiv : the preprint server for health sciences
PubMed ID:40909817
Avian influenza viruses (AIVs) are zoonotic pathogens that pose an increasing global threat due to their potential for significant economic losses in agriculture, spillover into humans, and the risk of a pandemic should human-to-human transmission occur. These concerns underscore the need for rapid, sensitive and specific tools to detect and
Establishing Methods to Monitor Influenza (A)H5N1 Virus in Dairy Cattle Milk, Massachusetts, USA.
Journal:Emerging infectious diseases
PubMed ID:40138725
Highly pathogenic avian influenza A(H5N1) virus has caused a multistate outbreak among US dairy cattle, spreading across 16 states and infecting hundreds of herds since its onset. We rapidly developed and optimized PCR-based detection assays and sequencing protocols to support H5N1 molecular surveillance. Using 214 retail milk samples from 20
Evaluation of Self-Collected Mouth Rinse Specimens for Coronavirus Disease 2019 Testing: A Pilot Study
Journal:COVID
PubMed ID:
Saliva specimens are widely used for coronavirus disease 2019 (COVID-19) testing using RT-qPCR due to their advantages over nasopharyngeal swabs of being non-invasive and self-collectable. However, saliva collection can be time-consuming in individuals with reduced saliva secretion, including those with diabetes, diseases involving salivary glands such as Sjögren’s syndrome, and
Interdependent RNA structural motifs at the 3'-terminus of the West Nile virus genome regulate viral growth.
Journal:bioRxiv : the preprint server for biology
PubMed ID:41959387
The RNA genome of West Nile Virus (WNV) folds into an elaborate series of RNA structural elements that are crucial for viral function. Among these elements, four pseudoknots (PKs) at the viral 3’-terminus, designated as SLII, SLIV, DBI, and DBII, are among the most crucial players in the overall flaviviral