Vybrant™ FLICA Caspase Apoptosis Assay Kits for flow cytometry
Vybrant™ FLICA Caspase Apoptosis Assay Kits for flow cytometry
Invitrogen™

Vybrant™ FLICA Caspase Apoptosis Assay Kits for flow cytometry

Detect apoptosis via flow cytometry with Vybrant FLICA Caspase Assays that detect poly and caspase-3/7/8 activities.
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카탈로그 번호라벨 또는 염료설명
V35118FAM, Hoechst 33342, Propidium IodideVybrant FAM Caspase-3 and -7 Assay Kit
V35117FMK, Hoechst 33342, Propidium IodideVybrant FAM Poly Caspases Assay Kit
V35119FAM, Hoechst 33344, Propidium IodideVybrant FAM Caspase-8 Assay Kit
카탈로그 번호 V35118
제품 가격(KRW)
415,000
Online offer
Ends: 31-Dec-2025
488,000
할인액 73,000 (15%)
25 assays
카트에 추가하기
라벨 또는 염료:
FAM, Hoechst 33342, Propidium Iodide
설명:
Vybrant FAM Caspase-3 and -7 Assay Kit
제품 가격(KRW)
415,000
Online offer
Ends: 31-Dec-2025
488,000
할인액 73,000 (15%)
25 assays
카트에 추가하기
Quickly detect caspase-mediated apoptosis by flow cytometry with Vybrant FAM caspase assay kits for poly-caspases and caspases 3 and 7. The Vybrant FAM caspase assay kits use fluorescent inhibitor of caspases (FLICA) methodology to detect and report caspase activity. Specifically, these caspase assay kits contain engineered FLICA substrates FAM-VAD-FMK (for poly-caspases), FAM-DEVD-FMK (for caspase-3/7), and FAM-LETD-FMK (for caspase-8). They also include Hoechst 33342 and propidium iodide stains, enabling simultaneous evaluation of membrane permeability and cell cycle by flow cytometry.
The Vybrant FAM caspase assay kits for flow cytometry employ a novel approach to detecting active caspases: the kits take advantage of FLICA methodology, which is an affinity label. This affinity label associates a fluoromethyl ketone (FMK) moiety, which can react covalently with a cysteine, with a caspase-specific amino acid sequence. Different amino acid recognition sequences are used to detect different caspases: valine-alanine-aspartic acid (VAD) for poly caspases (including caspase-1, -3, -4, -5, -6, -7, -8, and -9), aspartic acid-glutamic acid-valine-aspartic acid (DEVD) for caspase-3/7, and leucine-glutamic acid-threonine-aspartic acid (LETD) for caspase-8. A carboxyfluorescein (FAM) group is attached as a reporter.

The FLICA reagent is thought to interact with the enzymatic reactive center of an activated caspase via the recognition sequence, and then to attach covalently through the FMK moiety. The FLICA inhibitor is cell permeant and noncytotoxic. Unbound FLICA molecules diffuse out of the cell and are washed away; the remaining fluorescent signal is a direct measure of the amount of active caspase present at the time the inhibitor was added. The approximate excitation and emission peaks of the FLICA, propidium iodide, and Hoechst 33342 reagents are 488 nm/⁄530 nm, 535⁄ nm/6617 nm, and 350 nm/⁄461 nm, respectively. The detection reagents included within the individual Vybrant FAM Poly Caspases Assay, Caspase-3 and -7 Assay, and Caspase-8 Assay apoptosis kits are 488⁄⁄530 FAM-VAD-FMK reagent, 488/⁄530 FAM-DEVD-FMK, and 488/⁄530 FAM-LETD-FMK, respectively.
For Research Use Only. Not for use in diagnostic procedures.
사양
설명Vybrant FAM Caspase-3 and -7 Assay Kit
여기/방출FAM-DEVD-FMD: 388/530
PI: 535/617
Hoechst 33342: 350/461
유세포분석기 레이저 라인UV, 488
용도(장비)Flow Cytometer
키트 구성품1 vial FAM-DEVD-FMK caspase-3 and -7 reagent (FLICA reagent, lyophilized solid), 1 vial of Hoechst 33342 (400 μL, 1 mM in water), 1 vial of PI (1 mL, 250 μg/mL in water), 1 vial of DMSO (0.5 mL), 1 bottle of apoptosis fixative solution (10% formaldehyde with methanol in PBS, 6 mL), and 1 bottle of 10x apoptosis wash buffer.
라벨 유형Other Label(s) or Dye(s)
라벨 또는 염료FAM, Hoechst 33342, Propidium Iodide
제품라인Vybrant
제품 유형Caspase Assay Kit
수량25 assays
배송 조건Room Temperature
보관 요구 사항Store in refrigerator (2–8°C) and protect from light.
검출 방법Fluorescence
형식Tube
Unit Size25 assays

자주 묻는 질문(FAQ)

What are the fluorescence excitation/emission maxima for the FAM-DEVD-FMK FLICA reagent, Hoechst 33342, and propidium iodide supplied in the Vybrant FAM Caspase-3 and -7 Assay Kit, for flow cytometry?

FAM-DEVD-FMK FLICA reagent: 488/530 nm
Hoechst 33342: 350/461 nm
Propidium iodide: 535/617 nm

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

인용 및 참조 문헌 (20)

인용 및 참조 문헌
Abstract
Monocyte Chemoattractant Protein-Induced Protein 1 (MCPIP1) Enhances Angiogenic and Cardiomyogenic Potential of Murine Bone Marrow-Derived Mesenchymal Stem Cells.
Authors:Labedz-Maslowska A, Lipert B, Berdecka D, Kedracka-Krok S, Jankowska U, Kamycka E, Sekula M, Madeja Z, Dawn B, Jura J, Zuba-Surma EK,
Journal:
PubMed ID:26214508
'The current evidence suggests that beneficial effects of mesenchymal stem cells (MSCs) toward myocardial repair are largely due to paracrine actions of several factors. Although Monocyte chemoattractant protein-induced protein 1 (MCPIP1) is involved in the regulation of inflammatory response, apoptosis and angiogenesis, whether MCPIP1 plays any role in stem cell-induced ... More
Multiparametric evaluation of apoptosis: effects of standard cytotoxic agents and the cyanoguanidine CHS 828.
Authors:Lövborg H, Nygren P, Larsson R
Journal:Mol Cancer Ther
PubMed ID:15141009
'A multiparametric high-content screening assay for measurement of apoptosis was developed. HeLa cells and lymphoma U-937 cells were exposed to cytotoxic drugs in flat-bottomed optical microtiter plates. After incubation, the DNA-binding dye Hoechst 33342, fluorescein-tagged probes that covalently bind active caspases and chloromethyl-X-rosamine to detect mitochondrial membrane potential (MMP) were ... More
Flow cytometry-based apoptosis detection.
Authors:Wlodkowic D, Skommer J, Darzynkiewicz Z,
Journal:Methods Mol Biol
PubMed ID:19609746
'An apoptosing cell demonstrates multitude of characteristic morphological and biochemical features, which vary depending on the stimuli and the cell type. The gross majority of classical apoptotic hallmarks can be rapidly examined by flow and image cytometry. Cytometry thus became a technology of choice in diverse studies of cellular demise. ... More
BH3-only protein Noxa regulates apoptosis in activated B cells and controls high-affinity antibody formation.
Authors:Wensveen FM, Derks IA, van Gisbergen KP, de Bruin AM, Meijers JC, Yigittop H, Nolte MA, Eldering E, van Lier RA,
Journal:Blood
PubMed ID:22144184
The efficiency of humoral immune responses depends on the selective outgrowth of B cells and plasma cells that produce high affinity antibodies. The factors responsible for affinity maturation of B cell clones in the germinal center (GC) have been well established but selection mechanisms that allow clones to enter the ... More
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PubMed ID:21791709
In order to minimise the number of positive in vitro cytogenetic results which are not confirmed in rodent carcinogenicity tests, biological systems that are p53 and DNA repair proficient should be recommended. Moreover, an appropriate cytotoxicity parameter for top dose selection should be considered. Recent International Conference on Harmonisation draft ... More