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CD300E anticorps (FITC)

CD300E Reactivité: Humain FACS, IF Hôte: Souris Monoclonal UP-H2 FITC
N° du produit ABIN1112410
  • Antigène Voir toutes CD300E Anticorps
    CD300E (CD300e Molecule (CD300E))
    Reactivité
    • 35
    • 8
    Humain
    Hôte
    • 22
    • 13
    Souris
    Clonalité
    • 23
    • 12
    Monoclonal
    Conjugué
    • 9
    • 5
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp CD300E est conjugé à/à la FITC
    Application
    • 20
    • 14
    • 12
    • 5
    • 4
    • 2
    • 1
    Flow Cytometry (FACS), Immunofluorescence (IF)
    Attributs du produit
    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 Anticorps primaire
  • Indications d'application
    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.
    Commentaires

    Fluorescein isothiocyanate (Molecular Probes).

    Prélèvement de l'échantillon
    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.
    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.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    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.
    Stock
    4 °C
  • Antigène
    CD300E (CD300e Molecule (CD300E))
    Autre désignation
    IREM-2 (CD300E Produits)
    Synonymes
    anticorps BC034097, anticorps CLM2, anticorps Cd300le, anticorps TREM5, anticorps CD300LE, anticorps CLM-2, anticorps CMRF35-A5, anticorps IREM-2, anticorps IREM2, anticorps PIgR-2, anticorps PIgR2, anticorps CD300E molecule, anticorps CD300e molecule, anticorps Cd300e, anticorps CD300E
    Sujet
    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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