Click-iT™ Plus TUNEL Assay Kits for In Situ Apoptosis Detection
Click-iT™ Plus TUNEL Assay Kits for In Situ Apoptosis Detection
Invitrogen™

Click-iT™ Plus TUNEL Assay Kits for In Situ Apoptosis Detection

Green features
Detect apoptosis in cells and tissues samples with Click-iT Plus TUNEL Assay kits, which offer easy dye incorporation and can be multiplexed with GFP and RFP.
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Catalog NumberColorLabel or Dye
C10617GreenAlexa Fluor™ 488
C10618RedAlexa Fluor™ 594
C10619Far-RedAlexa Fluor™ 647
Catalog number C10617
Price (MXN)
-
Color:
Green
Label or Dye:
Alexa Fluor™ 488
Detect more apoptotic cells in tissues and cultured cell samples with the Click-iT Plus TUNEL Assay for In Situ Apoptosis Detection, which offers Alexa Fluor 488, 594, and 647 fluorescent dye options. This in situ apoptosis detection kit is optimized for tissue or cell samples and the dyes can be multiplexed with other dyes or proteins, such as GFP and RFP, and incorporated more readily into complex molecules due to their smaller size (compared with antibodies). This TUNEL assay kit is also very flexible and can be used to test 1–50 samples in a single experiment.
The Click-iT Plus TUNEL Alexa Fluor 488, 594, and 647 assays for in situ apoptosis detection can detect apoptotic cells in tissue and cultured cell samples through the incorporation of a small, highly specific labeling moiety and a bright fluorescent dye. After incorporation of the labeling moiety into DNA fragments, detection is achieved through a catalyzed “click” reaction using conditions mild enough to preserve the emitted fluorescent signal from GFP or RFP.

Other advantages of the Click-iT Plus TUNEL Assay for In Situ Apoptosis Detection include:
• Optimized for the detection of apoptotic cells in either tissue or cell samples
• Multiplex enabled—optimized to work with fluorescent dyes or proteins such as GFP and RFP
• Improved TUNEL assay—better label incorporation due to small reactive moiety
• Bright apoptotic signal—uses Alexa Fluor dyes, resulting in a stable, non-photobleaching fluorescent signal
• Flexibility—the assay can be configured to test 1–50 samples at a time

Fragmentation of cellular DNA is a hallmark of apoptosis. The TUNEL assay is the most widely used method to detect fragmented DNA in apoptotic cells or tissue samples. The TUNEL assay begins with incorporation of modified dUTP at the 3’-OH end of the fragmented DNA. The dUTP modification is often the addition of a fluorophore. Due to the size of the fluorophore, the modified dUTP can display lower than expected incorporation rates, which can affect the sensitivity of the TUNEL assay. Additionally, many fluorophores used in currently available TUNEL assay kits suffer from photobleaching and fluorescent spectral overlap issues, both of which reduce the sensitivity of and ability to multiplex the assay.

The Click-iT Plus TUNEL assay was developed to address these issues. The assay uses dUTP modified with an alkyne group (a small bio-orthogonal functional group), allowing the nucleotide to be more readily incorporated. After incorporation, a highly specific click reaction between the alkyne group and an Alexa Fluor picolyl azide fluorescent dye, and subsequent detection of that dye, results in a sensitive and specific assay for the detection of apoptotic cells or tissue samples. Because of its gentle reaction conditions, the Click-iT Plus TUNEL assay enables multiplexing with fluorescent proteins or dyes.

The Click-iT Plus TUNEL assay has been validated with several different formalin-fixed paraffin-embedded tissue types. In all cases, its ability to multiplex with fluorescent proteins and dyes was preserved. Additionally, the ability to stain actin using fluorescent-labeled phalloidin was also preserved.

The Click-iT Plus TUNEL assay contains all the reagents needed to detect apoptotic cells from either tissue or cell samples. The reagents supplied in this kit can be used to test 50 samples and can be configured to test 1–50 samples at a time.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
ColorGreen
DescriptionClick-iT Plus TUNEL Assay for In Situ Apoptosis Detection, Alexa Fluor™ 488 dye
Excitation/Emission490/525
For Use With (Equipment)Fluorescence Microscope
Green FeaturesLess hazardous
Label TypeAlexa Fluor™ Dyes
Label or DyeAlexa Fluor™ 488
No. of Reactions50 coverslips
Product LineClick-iT
Product TypeTUNEL Assay
Quantity1 kit
Shipping ConditionDry Ice
Storage RequirementsStore at ≤20°C and protect from light.
Detection MethodFluorescence
FormatCoverslip
Unit SizeEach

Frequently asked questions (FAQs)

What is the excitation/emission maxima of the Alexa Fluor 488 dye?

Alexa Fluor 488 has fluorescence excitation and emission maxima of 495/519 nm.

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

I will be performing a cell proliferation assay using Click-iT EdU kit. At what point can I stop overnight, or do I have to perform all the steps continuously?

One may store the sample after fixation overnight in PBS at 4oC. For longer storage (<1 week) , store in buffer with 1-2% formaldehyde or in formalin to limit microbial growth. If you use sodium azide as a microbial inhibitor, it must be completely removed prior to the Click-iT reaction.

Find additional tips, troubleshooting help, and resources within our Cell Viability, Proliferation, Cryopreservation, and Apoptosis Support Center.

I need to test cells for apoptosis after they have been formaldehyde-fixed and permeabilized. What dye or conjugate do you recommend? Will Annexin V conjugates work?

We do not recommend Annexin V for post-fix labeling, since fixation inactivates the function of the translocase; fixed samples would show mostly uniform labeling with Annexin V. The only options you have for apoptosis assays after fixation are to use an anti-caspase antibody or perform a TUNEL assay, such as with the Click-iT TUNEL Imaging kits.

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

Can I use Click-iT TUNEL Alexa Fluor Imaging Assays for Microscopy & HCS (Cat. No. C10246) for flow cytometry?

We have not validated the use of Click‐iT TUNEL assay for flow cytometry. Theoretically, any Click‐iT TUNEL assay for imaging can be adapted to be used with flow cytometry. In general, follow the protocol as provided but spin down the suspension cells after every step. Start with about 10∧6 cells at about 10∧7 cell/mL. Please note that flow cytometry is more sensitive than fluorescence imaging, so you should use between 1/5th to 1/10th of the azide dye detection reagent in the click reaction. All other concentrations of the click reaction reagents should stay the same. We recommend using the Click‐iT Plus TUNEL assays (C10617, C10618, C10619), as the detection reagent is provided in a separate vial, enabling you to modify the concentration used. The Click‐iT Plus TUNEL assay protocol can be found on the following link.

Find additional tips, troubleshooting help, and resources within our Cell Viability, Proliferation, Cryopreservation, and Apoptosis Support Center.

Can I use Click-iT Plus TUNEL Assay Kits for In Situ Apoptosis Detection (Cat. Nos. C10617, C10618, C10619) for whole mount immunofluorescence staining of zebrafish larvae?

Yes. The Click-iT Plus TUNEL Assay Kits for In Situ Apoptosis Detection (Cat. Nos. C10617, C10618, C10619) is optimized for use with tissues and should work on zebrafish larvae, although it has not been internally validated with zebrafish larvae.

Find additional tips, troubleshooting help, and resources within our Cell Viability, Proliferation, Cryopreservation, and Apoptosis Support Center.

Citations & References (9)

Citations & References
Abstract
Signaling and physiological activity of the NO-donating agent TNICthio in human blood lymphocytes, Jurkat and MCF7 cell lines.
Authors:Vasilieva SV, Petrishcheva MS, Yashkina EI, Osipov AN
Journal:Mol Biol Rep
PubMed ID:30637625
'Signaling and physiological activities of the crystalline tetranitrosyl iron complex with thiosulfate-a NO-donor (TNICthio) were first studied on human cells in conditions of mono and combined application of H' ... More
Characterization of NvLWamide-like neurons reveals stereotypy in Nematostella nerve net development.
Authors:Havrilak JA, Faltine-Gonzalez D, Wen Y, Fodera D, Simpson AC, Magie CR, Layden MJ
Journal:Dev Biol
PubMed ID:28888696
The organization of cnidarian nerve nets is traditionally described as diffuse with randomly arranged neurites that show minimal reproducibility between animals. However, most observations of nerve nets are conducted using cross-reactive antibodies that broadly label neurons, which potentially masks stereotyped patterns produced by individual neuronal subtypes. Additionally, many cnidarians species ... More
The Antidiabetic Drug Lobeglitazone Protects Mice From Lipogenesis-Induced Liver Injury via Mechanistic Target of Rapamycin Complex 1 Inhibition.
Authors:Lee YS, Park JS, Lee DH, Lee DK, Kwon SW, Lee BW, Bae SH
Journal:Front Endocrinol (Lausanne)
PubMed ID:30298052
Non-alcoholic fatty liver disease (NAFLD) is a metabolic disorder closely linked with type II diabetes (T2D). The progression of NAFLD is associated with the induction of lipogenesis through hyperactivation of the mechanistic target of rapamycin complex 1 (mTORC1) pathway. An increase in lipogenesis induces endoplasmic reticulum (ER) stress and accelerates ... More
Inhibition of WNT7A-ß-catenin signaling pathway sensitizes oral squamous cell carcinoma to cisplatin.
Authors:Tian J, Cui X, Feng Y, Gu L
Journal:Int J Clin Exp Pathol
PubMed ID:31949568
Oral squamous cell carcinoma (OSCC) is the most common type and most threatening head and neck cancer worldwide. Here, we aim to study the relationship between the WNT7A-ß-Catenin signaling pathway and the chemotherapy resistance of OSCC patients. We analyzed 42 OSCC patients and 19 adjacent non-tumor tissues, evaluated the expression ... More
Small Molecule GSK-J1 Affects Differentiation of Specific Neuronal Subtypes in Developing Rat Retina.
Authors:Raeisossadati R, Móvio MI, Walter LT, Takada SH, Del Debbio CB, Kihara AH
Journal:Mol Neurobiol
PubMed ID:29981055
Histone post-translational modification has been shown to play a pivotal role in regulating gene expression and fate determination during the development of the central nervous system. Application of pharmacological blockers that control histone methylation status has been considered a promising avenue to control abnormal developmental processes and diseases as well. ... More