BD Pharmingen™ FITC Annexin V Apoptosis Detection Kit II
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BD Pharmingen™ FITC Annexin V Apoptosis Detection Kit II

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品牌: BD Pharmingen
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    实验应用:
    Flow cytometry (Routinely Tested)
    Flow cytometry (Routinely Tested)
    产品介绍
    产品信息
    抗原名称
    ANNEXIN V
    简单描述
    Apoptosis is a normal physiologic process which occurs during embryonic development as well as in maintenence of tissue homeostasis. The apoptotic program is characterized by certain morphologic features, including loss of plasma membrane asymmetry and attachment, condensation of the cytoplasm and nucleus, and internucleosomal cleavage of DNA. Loss of plasma membrane is one of the earliest features. In apoptotic cells, the membrane phospholipid phosphatidylserine (PS) is translocated from the inner to the outer leaflet of the plasma membrane, thereby exposing PS to the external cellular environment. Annexin V is a 35-36 kDa Ca2+ dependent phospholipid-binding protein that has a high affinity for PS, and binds to cells with exposed PS. Annexin V may be conjugated to fluorochromes including FITC. This format retains its high affinity for PS and thus serves as a sensitive probe for flow cytometric analysis of cells that are undergoing apoptosis. Since externalization of PS occurs in the earlier stages of apoptosis, FITC Annexin V staining can identify apoptosis at an earlier stage than assays based on nuclear changes such as DNA fragmentation. FITC Annexin V staining precedes the loss of membrane integrity which accompanies the latest stages of cell death resulting from either apoptotic or necrotic processes. Therefore, staining with FITC Annexin V is typically used in conjunction with a vital dye such as propidium iodide (PI) or 7-Amino-Actinomycin (7-AAD) to allow the investigator to identify early apoptotic cells (PI negative, FITC Annexin V positive). Viable cells with intact membranes exclude PI, wheras the membranes of dead and damaged cells are permeable to PI. For example, cells that are considered viable are FITC Annexin V and PI negative; cells that are in early apoptosis are FITC Annexin V positive and PI negative; and cells that are in late apoptosis or already dead are are both FITC Annexin V and PI positive. This assay does not distinguish between cells that have undergone apoptotic death versus those that have died as a result of a necrotic pathway because in either case, the dead cells will stain with both Annexin-FITC and PI. However, when apoptosis is measured over time, cells can be often tracked from FITC Annexin V and PI negative (viable, or no measurable apoptosis), to FITC Annexin V positive and PI negative (early apoptosis, membrane integrity is present) and finally to FITC Annexin V and PI positive (end stage apoptosis and death). The movement of cells through these three stages suggests apoptosis. In contrast, a single observation indicating that cells are both FITC Annexin V and PI positive, in of itself, reveals less information about the process by which the cells underwent their demise.
    克隆号
    (RUO)
    组合货号
    51-6710AK/(2 to 8C)+51-6710BK/(max.-70C)
    BD化合物表
    • 描述
      数量/尺寸
      零件号
      EntrezGene ID
    • Purified Recombinant Annexin V
      100 µg (1 ea)
      51-65871A
      N/A
    • FITC Annexin V
      0.5 mL (1 ea)
      51-65874X
      N/A
    • Propidium Iodide Staining Solution
      2 mL (1 ea)
      51-66211E
      N/A
    • 10X Annexin V Binding Buffer
      50 mL (1 ea)
      51-66121E
      N/A
    应用
    实验应用
    Flow cytometry (Routinely Tested)
    目标/特异性
    Annexin V
    文献
    文献
    研发参考(10) 1. Andree HA, Reutelingsperger CP, Hauptmann R, Hemker HC, Hermens WT, Willems GM. Binding of vascular anticoagulant alpha (VAC alpha) to planar phospholipid bilayers. J Biol Chem. 1990; 265(9):4923-4928. (Biology). 2. Casciola-Rosen L, Rosen A, Petri M, Schlissel M. Surface blebs on apoptotic cells are sites of enhanced procoagulant activity: implications for coagulation events and antigenic spread in systemic lupus erythematosus. Proc Natl Acad Sci U S A. 1996; 93(4):1624-1629. (Biology). 3. Homburg CH, de Haas M, von dem Borne AE, Verhoeven AJ, Reutelingsperger CP, Roos D. Human neutrophils lose their surface Fc gamma RIII and acquire Annexin V binding sites during apoptosis in vitro. Blood. 1995; 85(2):532-540. (Biology). 4. Koopman G, Reutelingsperger CP, Kuijten GA, Keehnen RM, Pals ST, van Oers MH. Annexin V for flow cytometric detection of phosphatidylserine expression on B cells undergoing apoptosis. Blood. 1994; 84(5):1415-1420. (Biology). 5. Martin SJ, Reutelingsperger CP, McGahon AJ, et al. Early redistribution of plasma membrane phosphatidylserine is a general feature of apoptosis regardless of the initiating stimulus: inhibition by overexpression of Bcl-2 and Abl. J Exp Med. 1995; 182(5):1545-1556. (Biology). 6. O'Brien MC, Bolton WE. Comparison of cell viability probes compatible with fixation and permeabilization for combined surface and intracellular staining in flow cytometry. Cytometry. 1995; 19(3):243-255. (Biology). 7. Raynal P, Pollard HB. Annexins: the problem of assessing the biological role for a gene family of multifunctional calcium- and phospholipid-binding proteins. Biochim Biophys Acta. 1994; 1197(1):63-93. (Biology). 8. Schmid I, Krall WJ, Uittenbogaart CH, Braun J, Giorgi JV. Dead cell discrimination with 7-amino-actinomycin D in combination with dual color immunofluorescence in single laser flow cytometry. Cytometry. 1992; 13(2):204-208. (Biology). 9. Vermes I, Haanen C, Steffens-Nakken H, Reutelingsperger C. A novel assay for apoptosis. Flow cytometric detection of phosphatidylserine expression on early apoptotic cells using fluorescein labelled Annexin V. J Immunol Methods. 1995; 184(1):39-51. (Biology). 10. van Engeland M, Ramaekers FC, Schutte B, Reutelingsperger CP. A novel assay to measure loss of plasma membrane asymmetry during apoptosis of adherent cells in culture. Cytometry. 1996; 24(2):131-139. (Biology).

    参考图片

    Flow Cytometric Analysis of FITC Annexin V staining and blocking. Jurkat cells (Human T-cell leukemia; ATCC TIB-152) were either untreated (top/bottom far left and middle-right panels) or were induced to undergo apoptosis by treatment with camptothecin (12 µM, 4 hours) (top/bottom middle-left and far right panels). Cells were then incubated with FITC Annexin V in a buffer containing propidium iodide (top/bottom far left and middle left panels) or with purified recombinant Annexin V (top/bottom far right and middle-right panels) in order to block FITC Annexin V binding sites prior to adding FITC Annexin-V. After camptothecin treatment (4 hours), a population of cells was FITC Annexin V positive (bottom middle-left panel, M2). FITC Annexin V staining was blocked when cells were first incubated with purified recombinant Annexin V (bottom far right panel, M2). As expected, the cell population that was not treated was primarily Annexin V negative (bottom far left panel, M1). The small number of Annexin V positive cells in the untreated population likely represents a basal level of apoptosis (bottom far left panel, M2).

    Flow Cytometric Analysis of FITC Annexin V staining and blocking. Jurkat cells (Human T-cell leukemia; ATCC TIB-152) were either untreated (top/bottom far left and middle-right panels) or were induced to undergo apoptosis by treatment with camptothecin (12 µM, 4 hours) (top/bottom middle-left and far right panels). Cells were then incubated with FITC Annexin V in a buffer containing propidium iodide (top/bottom far left and middle left panels) or with purified recombinant Annexin V (top/bottom far right and middle-right panels) in order to block FITC Annexin V binding sites prior to adding FITC Annexin-V. After camptothecin treatment (4 hours), a population of cells was FITC Annexin V positive (bottom middle-left panel, M2). FITC Annexin V staining was blocked when cells were first incubated with purified recombinant Annexin V (bottom far right panel, M2). As expected, the cell population that was not treated was primarily Annexin V negative (bottom far left panel, M1). The small number of Annexin V positive cells in the untreated population likely represents a basal level of apoptosis (bottom far left panel, M2).

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    货号:
    556570
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