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Exosome Isolation Reagent for Plasma

Cat.No: ATR-SPS-0036 Datasheet

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Product Details Related Products
Product Name Exosome Isolation Reagent for Plasma
Catalog No. ATR-SPS-0036
Description A plasma-specific precipitation system for isolating exosomes without ultracentrifugation. Low-speed collection supports intact vesicle morphology, while the included protease can be used to reduce abundant plasma-protein interference when surface-protein analysis is not required.
Intended Use Isolation of plasma-derived exosomes for protein studies, RNA analysis, high-throughput sequencing and cell co-culture research.
Principle / Technology Optional protease pretreatment followed by selective extracellular-vesicle precipitation and low-speed centrifugation.
Detection Method Downstream nanoparticle, protein, RNA and sequencing analyses.
Sample Type Plasma.
Performance Range / Specifications Minimum recommended plasma input: 0.5 mL. Recovered pellets may be resuspended in 1× PBS or directly processed with downstream lysis reagents.
Reaction Conditions / Protocol When appropriate, pretreat plasma with the supplied protease, add the isolation reagent and collect the precipitated vesicles by low-speed centrifugation.
Components / Formulation Plasma exosome isolation reagent and Proteinase K at 20 mg/mL.
Storage Conditions Store the isolation reagent at 2-8°C and Proteinase K at -30 to -15°C.
Package Specifications 10 mL isolation reagent; 2 × 900 µL Proteinase K.
Product Form Liquid precipitation reagent with protease component.
Key Features No ultracentrifuge required; low starting-volume requirement; optional plasma-protein digestion; rapid low-speed workflow; morphology-preserving isolation.
Compatibility Protein analysis, RNA extraction, miRNA analysis, high-throughput sequencing and cell co-culture workflows.
Application Notes / Precautions Proteinase K may digest exosomal surface proteins. Omit the protease pretreatment when downstream analysis depends on intact surface proteins.

For research use only, not for clinical use.

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