Image-iT™ LIVE Red and Green Caspase Apoptosis Detection Kits for microscopy
Image-iT™ LIVE Red and Green Caspase Apoptosis Detection Kits for microscopy
Actual product may vary
Invitrogen™

Image-iT™ LIVE Red and Green Caspase Apoptosis Detection Kits for microscopy

Detect apoptosis via microscopy, including fluorescence microscopy and HCS, with Image-iT LIVE Red and Green Caspase Apoptosis Detection Kits that report poly and caspase-3/7 activities.
Have Questions?
보기 방식 변경buttonViewtableView
카탈로그 번호색상효소라벨 또는 염료
I35101Red, Green, BluePoly CaspasesSR-VAD-FMK, SYTOX Green, Hoechst 33342
I35102Red, Green, BlueCaspase 3/7SR-DEVD-FMK, SYTOX Green, Hoechst 33342
I35104Green, Red, BluePoly CaspasesFAM-VAD-FMK, Propidium Iodide, Hoechst 33342
I35106Green, Red, BlueCaspase 3/7FAM-DEVD-FMK, Propidium Iodide, Hoechst 33342
카탈로그 번호 I35101
제품 가격(KRW)
618,000
キャンペーン価格
Ends: 31-Dec-2025
727,000
할인액 109,000 (15%)
Each
카트에 추가하기
색상:
Red, Green, Blue
효소:
Poly Caspases
라벨 또는 염료:
SR-VAD-FMK, SYTOX Green, Hoechst 33342
제품 가격(KRW)
618,000
キャンペーン価格
Ends: 31-Dec-2025
727,000
할인액 109,000 (15%)
Each
카트에 추가하기
Detect and evaluate caspase activation, membrane permeability, and cell cycle using Image-iT LIVE red and green poly and caspase-3 and-7 apoptosis detection kits for microscopy, including fluorescence microscopy and high content screening (HCS). The Image-iT LIVE red and green caspase detection kits use fluorescent inhibitor of caspases (FLICA) methodology to detect and report caspase activity, a measure of cell apoptosis. Specifically, the Image-iT LIVE red and green caspase detection kits contain the substrates SR-VAD-FMK and SR-DEVD-FMK (for red fluorescence), or FAM-VAD-FMK and FAM-DEVD-FMK (green fluorescence), for poly caspases and caspase-3/7 detection, respectively. They also include Hoechst 33342 and propidium iodide stains, enabling simultaneous evaluation of membrane permeability and cell cycle by microscopy and HCS.
The Image-iT LIVE red and green caspase detection kits for microscopy employ a novel approach to detecting active caspases: both assay kits take advantage of a fluorescent inhibitor of caspases (FLICA) methodology, which is an affinity label. This reagent 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), and aspartic acid-glutamic acid-valine-aspartic acid (DEVD) for caspase 3/7. A sulforhodamine (SR) group or 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 red or green 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 Image-iT LIVE Red Poly Caspases, Red Caspase-3/7, Green Poly Caspases, and Green Caspase-3/7 Detection kits are SR-VAD-FMK, SR-DEVD-FMK, FAM-VAD-FMK, and FAM-DEVD-FMK, respectively.
For Research Use Only. Not for use in diagnostic procedures.
사양
색상Red, Green, Blue
설명Image-iT LIVE Red Poly Caspases Detection Kit
효소Poly Caspases
여기/방출SR-VAD-FMK: 550/595
SYTOX Green: 504/523
Hoechst 33342: 350/461
용도(장비)Fluorescence Microscope
라벨 유형Other Label(s) or Dye(s)
라벨 또는 염료SR-VAD-FMK, SYTOX Green, Hoechst 33342
반응 수25 tests (labeling volumes of 300μL)
제품라인Image-iT
제품 유형Caspase Assay Kit
수량1 kit
배송 조건Room Temperature
보관 요구 사항Store in refrigerator (2–8°C) and protect from light.
검출 방법Fluorescence
형식Slide
Unit SizeEach

인용 및 참조 문헌 (6)

인용 및 참조 문헌
Abstract
In vitro studies with renal proximal tubule cells show direct cytotoxicity of Androctonus australis hector scorpion venom triggered by oxidative stress, caspase activation and apoptosis.
Authors:Saidani C, Hammoudi-Triki D, Laraba-Djebari F, Taub M,
Journal:Toxicon
PubMed ID:27470530
'Scorpion envenomation injures a number of organs, including the kidney. Mechanisms proposed to explain the renal tubule injury include direct effects of venom on tubule epithelial cells, as well as indirect effects of the autonomic nervous system, and inflammation. Here, we report direct effects of Androctonus australis hector (Aah) scorpion ... More
A feedback loop between nonsense-mediated decay and the retrogene DUX4 in facioscapulohumeral muscular dystrophy.
Authors:
Journal:Elife
PubMed ID:25564732
Legionella pneumophila Modulates Mitochondrial Dynamics to Trigger Metabolic Repurposing of Infected Macrophages.
Authors:
Journal:Cell Host Microbe
PubMed ID:28867389
Morphokinetic-related response to stress in individually cultured bovine embryos.
Authors:Silva T, Santos EC, Annes K, Soares CA, Leite RF, Lima CB, Milazzotto MP
Journal:Theriogenology
PubMed ID:27298151
The kinetics of in vitro-produced (IVP) bovine embryos is related to embryo viability, metabolism, and epigenetic patterns. Therefore, we believe that embryos with different speeds of development also respond differently to stress. In the present study, we performed global metabolic analysis (matrix-assisted laser desorption ionization time of flight mass spectrometry [MALDI-TOF]) ... More
The role of RhoA in retrograde neuronal death and axon regeneration after spinal cord injury.
Authors:Hu J, Zhang G, Rodemer W, Jin LQ, Shifman M, Selzer ME
Journal:Neurobiol Dis
PubMed ID:27888137
Paralysis following spinal cord injury (SCI) is due to interruption of axons and their failure to regenerate. It has been suggested that the small GTPase RhoA may be an intracellular signaling convergence point for several types of growth-inhibiting extracellular molecules. Even if this is true in vitro, it is not ... More