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CaspGLOWTM Fluorescein Active Caspase-2 Staining Kit

ABIN412025 产品详细信息, 供应商: Log in to see
抗原
  • xCaspase-2
  • Caspase-2
  • ICH-1
  • Nedd2
  • CASP-2
  • ICH1
  • NEDD-2
  • NEDD2
  • PPP1R57
  • ICH-1L/1S
  • ICH1L1S
  • caspase-2-like
  • caspase-2
  • caspase 2
  • caspase 2, apoptosis-related cysteine peptidase
  • LOC100050611
  • xCaspase-2
  • CpipJ_CPIJ008254
  • Casp2
  • LOC100101590
  • CASP2
  • LOC100521118
适用
哺乳动物
7
6
3
1
1
1
1
1
1
1
1
1
1
应用范围
Detection (D), Fluorescence Microscopy (FM), Flow Cytometry (FACS)
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原理 The CaspGLOW™ Fluorescein Active Caspase-2 Staining Kit provides a convenient means for sensitive detection of activated caspase-2 in living cells. The assay utilizes the caspase-2 inhibitor, VDVAD-FMK, conjugated to FITC (FITC-VDVAD-FMK) as a marker. FITC-VDVAD-FMK is cell permeable, nontoxic, and irreversibly binds to activated caspase-2 in apoptotic cells.
品牌 CaspGLOW™
样品类型 Cell Samples
检测方法 Fluorometric
特异性 The CaspGLOW™ Fluorescein Active Caspase-2 Staining Kit provides a convenient means for sensitive detection of activated caspase-2 in living cells. The assay utilizes the caspase-2 inhibitor, VDVAD-FMK, conjugated to FITC (FITC-VDVAD-FMK) as a marker. FITC-VDVAD-FMK is cell permeable, nontoxic, and irreversibly binds to activated caspase-2 in apoptotic cells. The FITC label allows for direct detection of activated caspases in apoptotic cells by fluorescence microscopy, flow cytometry, or fluorescence plate reader.
产品特性 CaspGLOWTM Fluorescein Active Caspase-2 Staining Kit: Convenient & Sensitive Kit to Detect Activated Caspases-2 in Living Cells. Detection Method: Fluorescence Microscopy, Flow Cytometry or Fluorescence Plate Reader.
组件 FITC-VDVAD-FMK
Wash Buffer
Z-VAD-FMK
别名 Caspase-2 (CASP2 ELISA Kit 摘要)
背景 Activation of caspases plays a central role in apoptosis. The CaspGLOW™ Fluorescein Active Caspase-2 Staining Kit provides a convenient means for sensitive detection of activated caspase-2 in living cells. The assay utilizes the caspase-2 inhibitor, VDVAD-FMK, conjugated to FITC (FITC-VDVAD-FMK) as a marker. FITC-VDVAD-FMK is cell permeable, nontoxic, and irreversibly binds to activated caspase-2 in apoptotic cells.
研究领域 Apoptosis/Necrosis, Cancer, Autophagy
应用备注 Sensitive detection of activated caspase-2 in living cells.
说明

Further details regarding sample type: Live cells

实验流程 A. Staining Procedure:
1. Induce apoptosis in cells (1 x 10^6 /mL) by desired method. Concurrently incubate a control culture without induction. An additional negative control can be prepared by adding the caspase inhibitor Z-VAD-FMK at 1 µL/mL to an induced culture to inhibit caspase-2 activation.
2. Aliquot 300 µL each of the induced and control cultures into eppendorf tubes.
3. Add 1 µL of FITC-VDVAD-FMK into each tube and incubate for 0.5-1 hour at 37 °C incubator with 5 % CO 2.
4. Centrifuge cells at 3000 rpm for 5 minutes and remove supernatant.
5. Resuspend cells in 0.5 mL of Wash Buffer, and centrifuge again.
6. Repeat Step
5. Proceed to B, C, or D depending on methods of analysis. B. Quantification by Flow Cytometry: For flow cytometric analysis, resuspend cells in 300 µL of Wash Buffer. Keep samples on ice. Analyzing samples by flow cytometry using the FL-1 channel. C. Detection by Fluorescence Microscopy: For fluorescence microscopic analysis, resuspend cells in 100 µL Wash Buffer. Transfer one drop of the cell suspension onto a microslide and cover with a coverslip. Observe cells under a fluorescence microscope using FITC filter. Caspase positive cells appear to have brighter green signals, whereas caspase negative control cells show much weaker signal. D. Analysis by Fluorescence Plate Reader: For analysis with fluorescence plate reader, resuspend cells in 100 µL Wash Buffer and then transfer the cell suspension into each well in the black microtiter plate. Measure the fluorescence intensity at Ex. = 485 nm and Em. = 535 nm. For control, use wells containing unlabeled cells.
限制 仅限研究用
储存条件 -20 °C
有效期 6-12 months
有引用在: Espín, Roca, Candel, Sepulcre, González-Rosa, Alcaraz-Pérez, Meseguer, Cayuela, Mercader, Mulero: "TNF receptors regulate vascular homeostasis in zebrafish through a caspase-8, caspase-2 and P53 apoptotic program that bypasses caspase-3." in: Disease models & mechanisms, Vol. 6, Issue 2, pp. 383-96, 2013 (PubMed).

Ito, Yip, Katz, Fonseca, Hedley, Chow, Xu, Wood, Bastianutto, Schimmer, Kelley, Liu: "Potential use of cetrimonium bromide as an apoptosis-promoting anticancer agent for head and neck cancer." in: Molecular pharmacology, Vol. 76, Issue 5, pp. 969-83, 2009 (PubMed).

Yip, Ito, Mao, Au, Hedley, Mocanu, Bastianutto, Schimmer, Liu: "Potential use of alexidine dihydrochloride as an apoptosis-promoting anticancer agent." in: Molecular cancer therapeutics, Vol. 5, Issue 9, pp. 2234-40, 2006 (PubMed).

Abdel-Latif, Murray, Renberg, ONeill, Porter, Jensen, Johnson: "Cell death in bovine parvovirus-infected embryonic bovine tracheal cells is mediated by necrosis rather than apoptosis." in: The Journal of general virology, Vol. 87, Issue Pt 9, pp. 2539-48, 2006 (PubMed).