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Annexin V Apoptosis Detection Kit CF-Blue

FACS Reactivité: Chemical Fluorometric Blood, Cell Culture Cells
N° du produit ABIN2669908

Aperçu rapide pour Annexin V Apoptosis Detection Kit CF-Blue (ABIN2669908)

Antigène

Voir toutes Annexin V (ANXA5) Kits
Annexin V (ANXA5) (Annexin A5 (ANXA5))

Reactivité

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Chemical

Méthode de détection

Fluorometric

Application

Flow Cytometry (FACS)

Type d'échantillon

Blood, Cell Culture Cells
  • Conjugué

    CF405M

    Fonction

    The kit can identify and quantitate apoptotic cells on a single-cell basis by flow cytometry. CF-Blue is an alternative to Pacific Blue dye®, BD HorizonTM V450

    Attributs du produit

    CF-Blue is an alternative to Pacific Blue dye®, BD HorizonTM V450. Staining cells simultaneously with Annexin V- CFTMBlue and the non-vital dye propidium iodide (red fluorescence) allows (bivariate analysis) the discrimination of intact cells (Annexin V- CFTMBlue negative, PI negative), early apoptotic (Annexin V- CFTMBlue positive, PI negative) and late apoptotic or necrotic cells (Annexin V- CFTMBlue positive, PI positive).

    Ingrédients

    • 100 Tests of AnnexinV CF-Blue
    • 100 Tests of PI
    • 10X Binding Buffer
  • Matériel non inclus

    • pipettes
    • ,
    • tubes
    • ,
    • flow cytometry machine
  • Indications d'application

    Optimal working dilution should be determined by the investigator.

    Commentaires

    Samples were tested on Flow Cytometry Induce apoptosis in cells using the desired method is not included in this time. For instance, Jurkat cells (T-cell leukemia, human) treated with 6 μM camptothecin for four hours.

    Volume d'échantillon

    5 μL

    Durée du test

    < 1 h

    Protocole

    Staining cells protocol with Annexin- CFTMBlue. Flow Cytometry
    1. Prepare Annexin V Binding Buffer: 10 mM Hepes/NaOH ( pH 7,4) 140 mM NaCl, 2,5 mM CaCl2. .
    2. Induce apoptosis in cells using the desired method. A negative control should be prepared by untreated cells, that is used to define the basal level of apoptotic and necrotic or dead cells.
    3. Harvest the cells after the apoptosis induction and wash in temperate phosphate-buffered saline (PBS).
    4. Wash cells twice with temperate PBS and resuspend cells in 1 X Annexin-binding buffer at a concentration 1 x 106 cells/mL.
    5. Add 5 μL of the Annexin V- CFTMBlue and 5 μL of PI, to each 100 μL of cell suspension.
    6. Incubate the cells at room temperature for 15 minutes at room temperature (25 °C) in the dark.
    7. After incubation period, add 400 μL of 1X Annexin-binding buffer. Analyze by flow cytometry within one hour.

    Restrictions

    For Research Use only
  • Agent conservateur

    Sodium azide

    Précaution d'utilisation

    Reagents contain sodium azide. Sodium azide under acid conditions yields hydrazoic acid, an extremely toxic compound. Azide compounds should be diluted with running water before being discarded. These conditions are recommended to avoid deposits in plumbing where explosive conditions may develop.
    Do not pipet by mouth.
    Samples should be handled as if capable of transmitting infection. Appropriate disposal methods should be used.
    The sample preparation procedure employs a fixative (formaldehyde). Contact is to be avoided with skin or mucous membranes

    Conseil sur la manipulation

    Light exposure should be avoided. Use dim light during handling, incubation with cells and prior to analysis.

    Stock

    4 °C
  • Antigène

    Annexin V (ANXA5) (Annexin A5 (ANXA5))

    Autre désignation

    Annexin V

    Poids moléculaire

    35 kDa
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