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CD300E antibody (PE)

CD300E Reactivity: Human FACS, IF Host: Mouse Monoclonal UP-H2 PE
Catalog No. ABIN1112411
  • Target See all CD300E Antibodies
    CD300E (CD300e Molecule (CD300E))
    Reactivity
    • 35
    • 8
    Human
    Host
    • 22
    • 13
    Mouse
    Clonality
    • 23
    • 12
    Monoclonal
    Conjugate
    • 9
    • 5
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CD300E antibody is conjugated to PE
    Application
    • 20
    • 14
    • 12
    • 5
    • 4
    • 2
    • 1
    Flow Cytometry (FACS), Immunofluorescence (IF)
    Characteristics
    Monoclonal Mouse Anti-Human IREM-2 is recommended for use in flow cytometry for identification of mature hematopoietic cells of the monocytic and myeloid dendritic cell lineages. This marker is specifically present on monocytic cell subset..
    Clone
    UP-H2
    Isotype
    IgG2a
    Top Product
    Discover our top product CD300E Primary Antibody
  • Application Notes
    It is recommended for use in flow cytometry. This reagent is effective for direct immunofluorescence staining of human tissue for flow cytometric analysis using 20 µl/10^6 cells.
    Comment

    R-Phycoerythrin (Europa Bioproducts, Ely, Cambridge).

    Sample Collection
    1. Transfer 100 µl of anticoagulated (EDTA) blood to a 12 x 75 mm polystyrene test tube (10 P6 P cells). 2. Add 20 µl of anti- IREM-2 PE and mix gently with a vortex mixer. The 20 µl is a guideline only, the optimal volume should be determined by the individual laboratory. 3. The recommended negative control is a non-reactive PE-conjugated antibody of the same isotype. 4. Incubate in the dark at room temperature at 4°C for 30 minutes or at room temperature (20-25 °C) for 15 minutes. 5. Add 1,5 ml of Lysing Solution to each sample and mix gently with a vortex mixer. Incubate for 10 minutes at room temperature in the dark. 6. Centrifuge at 1000 x g for 5 minutes. Gently aspirate the supernatant and discard it leaving approximately 50 µl of fluid. 7. Add 2 ml 0.01 mol/l PBS (It betters that it containing 2% bovine serum albumin) and resuspend the cells by using a vortex mixer. 8. Centrifuge at 1000 x g for 5 minutes. Gently aspirate the supernatant and discard it leaving approximately 50 µl of fluid. 9. Resuspend pellet in an appropriate fluid for flow cytometry, e.g. 0.3 ml PBS. The PBS should contain 1% paraformaldehyde (fixative) if samples are not analysed the same day. 10. Analyse on a flow cytometer or store at 2-8 °C in the dark until analysis. Samples can be run up to 24 hours after lysis.
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    The conjugate is provided in liquid form in buffer containing 1% bovine serum albumin (BSA) and 0,09% Sodium azide, pH 7.2.
    Preservative
    Sodium azide
    Precaution of Use
    1. The device is not intended for clinical use including diagnosis, prognosis, and monitoring of a disease state, and it must not be used in conjunction with patient records or treatment. 2. This product contains Sodium azide (NaN3), a chemical highly toxic in pure form. At product concentrations, though not classified as hazardous, Sodium azide may react with lead and copper plumbing to form highly explosive build-ups of metal azides. Upon disposal, flush with large volumes of water to prevent metal azide build-up in plumbing. 3. As with any product derived from biological sources, proper handling procedures should be used.
    Storage
    4 °C
  • Target
    CD300E (CD300e Molecule (CD300E))
    Alternative Name
    IREM-2 (CD300E Products)
    Synonyms
    BC034097 antibody, CLM2 antibody, Cd300le antibody, TREM5 antibody, CD300LE antibody, CLM-2 antibody, CMRF35-A5 antibody, IREM-2 antibody, IREM2 antibody, PIgR-2 antibody, PIgR2 antibody, CD300E molecule antibody, CD300e molecule antibody, Cd300e antibody, CD300E antibody
    Background
    The anti-Irem-2 is specific for monocytes and myeloid dendritic cells lineages. normal peripheral blood should be positive for at least 80% of monocytes. The antibody can be used to classify the different types of myeloid leukaemias, especially those with monocytic component.
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