MagMAX™ Prime Viral/Pathogen NA Isolation Kit
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 of詳細を見る
製品番号(カタログ番号)数量
A58145Up to 600 reactions
製品番号(カタログ番号) A58145
価格(JPY)
175,500
Each
数量:
Up to 600 reactions
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

研究用にのみ使用できます。
仕様
ビーズタイプMagnetic
Clear
使用対象(アプリケーション)Next-Generation Sequencing, RT-PCR (Endpoint), Real-Time PCR
高スループット適合性High-throughput Compatible, Automated Protocols
主機能Isolate and purify viral, bacterial, parasitic, and fungal nucleic acid
反応数Up to 600 Reactions
核酸タイプDNA/RNA
製品ラインMagMAX
製品タイプReagent
数量Up to 600 reactions
サンプルタイプSwabs in Transport Media, Saliva, Urine, Serum, Plasma
サンプル量200–400 μL
品質保持期間2 Years
出荷条件室温
ターゲットViral, Bacterial, Parasitic, and Fungal Nucleic Acid
フォーマットキット
Isolation TechnologyBeads
Unit SizeEach
組成および保存条件

• 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.

引用および参考文献 (4)

引用および参考文献
Abstract
Evaluation of Self-Collected Mouth Rinse Specimens for Coronavirus Disease 2019 Testing: A Pilot Study
Authors:Kento Fukano; Junko S. Takeuchi; Azusa Kamikawa; Wataru Sugiura
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 ... More
Interdependent RNA structural motifs at the 3'-terminus of the West Nile virus genome regulate viral growth.
Authors:Tsao LH,Brackney DE,Pyle AM
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 ... More
Saliva as a Reliable and Non-invasive Sample for Detecting Influenza A in Severe Acute Respiratory Infection Cases.
Authors:Takeuchi JS,Matsunaga N,Tsukada A,Iwamoto N,Fuwa N,Ichikawa T,Kato Y,Tomita Y,Kitagawa H,Yamato M,Aoyagi T,Hagiya H,Hase R,Hatakeyama S,Inaba T,Izumikawa K,Takesue Y,Kimura M,Ohmagari N
Journal:Cureus
PubMed ID:41658625
Background Nasopharyngeal swab sampling remains the gold standard for influenza diagnosis; however, it has several limitations, including dependence on medical staff, invasiveness, potential for nosocomial transmission, and occupational exposure risk. Non-invasive alternatives, such as saliva and nasal vestibular swabs, may improve patient comfort and participation in clinical studies. In addition, ... More
Bead-based approaches for increased sensitivity and multiplexing of CRISPR diagnostics.
Authors:Siddiqui SM,Welch NL,Nguyen TG,Razmi A,Chang T,Senft R,Arizti-Sanz J,Mirhashemi ME,Stirling DR,Ackerman CM,Cimini BA,Blainey PC,Sabeti PC,Myhrvold C
Journal:Nature biomedical engineering
PubMed ID:40983646
CRISPR-based diagnostics have emerged as a promising tool for fast, accurate and portable pathogen detection. There has been rapid progress in pre-amplification processes and CRISPR-related enzymes used in these approaches, but the development of reporter systems and reaction platforms has lagged behind. In this paper, we develop bead-based techniques to ... More