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Exosome Purification and Analysis Kit (Urine)

FACS Reactivity: Human Fluorometric Urine
Catalog No. ABIN5633281
  • Reactivity
    Human
    Detection Method
    Fluorometric
    Conjugate
    PE
    Application
    Flow Cytometry (FACS)
    Purpose
    Exosome purification and FACS analysis kit of exosomes derived from human urine
    Brand
    ExoStep™
    Sample Type
    Urine
    Characteristics
    The kit is a simple immunobead assay for isolation/detection of exosome, using a bead-bound anti-CD63 capture antibody and a fluorochrome conjugated anti-CD9 detection antibody. The kit provides reproducible results and can be run in parallel to exosome immunophenotyping.
    Components
    CD63+ capture beads Anti-CD9 biotin Streptavidin-Phycoerythrin (PE) Assay Buffer 10X
    Material not included
    • Pre-enriched exosomes by ultra-centrifugation. • Magnetic Rack, MagneSphere(R) Mag. Sep. Stand 12-hole, 12x75mm (PROMEGA, Ref Z5343). • 12x75 mm Polystyrene Round Bottom Tubes (cytometer
  • tubes
  • ). • Sterile syringe filter with a 0.22 μm pore. (EMD Millipore, Ref SLGSV255F) • Syringe of adequate volume
  • Application Notes
    Isolate and purify exosomes by FACS with reproducible results. It allows also immunophenotyping of the captured exosomes
    Comment

    5 hours for enrichement the sample+ Overnight Incubation+ 1 hour of protocol

    Sample Volume
    50 μL
    Assay Time
    6 h
    Reagent Preparation

    Reagents ready to use.

    Restrictions
    For Research Use only
  • Buffer
    The reagent is provided in aqueous buffered solution containing protein stabilizer, and ≤0.09% sodium azide (NaN3)
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C
    Storage Comment
    Store in the dark at 2-8 °C
  • Background
    Exosomes are small extracellular vesicles that are released from cells upon fusion of an intermediate endocytic compartment, the multivesicular body (MVB)1, with the plasma membrane. They are thought to provide a means of intercellular communication and of transmission of macromolecules between cells allowing the spread of proteins, lipids, mRNA, miRNA and DNA and as contributing factors in the development of several diseases.
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