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CD300E Antikörper (FITC)

CD300E Reaktivität: Human FACS, IF Wirt: Maus Monoclonal UP-H2 FITC
Produktnummer ABIN1112410
  • Target Alle CD300E Antikörper anzeigen
    CD300E (CD300e Molecule (CD300E))
    Reaktivität
    • 33
    • 8
    Human
    Wirt
    • 22
    • 11
    Maus
    Klonalität
    • 23
    • 10
    Monoklonal
    Konjugat
    • 9
    • 5
    • 4
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser CD300E Antikörper ist konjugiert mit FITC
    Applikation
    • 20
    • 14
    • 10
    • 5
    • 4
    • 2
    • 1
    Flow Cytometry (FACS), Immunofluorescence (IF)
    Produktmerkmale
    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..
    Klon
    UP-H2
    Isotyp
    IgG2a
    Top Product
    Discover our top product CD300E Primärantikörper
  • Applikationshinweise
    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.
    Kommentare

    Fluorescein isothiocyanate (Molecular Probes).

    Probennahme
    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 FITC 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 FITC-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.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • 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.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    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.
    Lagerung
    4 °C
  • Target
    CD300E (CD300e Molecule (CD300E))
    Andere Bezeichnung
    IREM-2 (CD300E Produkte)
    Synonyme
    BC034097 antikoerper, CLM2 antikoerper, Cd300le antikoerper, TREM5 antikoerper, CD300LE antikoerper, CLM-2 antikoerper, CMRF35-A5 antikoerper, IREM-2 antikoerper, IREM2 antikoerper, PIgR-2 antikoerper, PIgR2 antikoerper, CD300E molecule antikoerper, CD300e molecule antikoerper, Cd300e antikoerper, CD300E antikoerper
    Hintergrund
    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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