Click-iT™ TUNEL Colorimetric IHC Detection Kit
FWS 제품은 특정 승인이 필요하므로 배송이 약 2-3주 더 소요됩니다.
Click-iT™ TUNEL Colorimetric IHC Detection Kit
Invitrogen™

Click-iT™ TUNEL Colorimetric IHC Detection Kit

The Click-iT™ TUNEL Colorimetric IHC Detection Kit is used to identify apoptotic cells in tissue and cultured cell samples through자세히 알아보기
Have Questions?
카탈로그 번호수량
C106251 Kit
카탈로그 번호 C10625
제품 가격(KRW)
1,174,000
線上優惠
Ends: 31-Dec-2025
1,381,000
할인액 207,000 (15%)
Each
카트에 추가하기
수량:
1 Kit
제품 가격(KRW)
1,174,000
線上優惠
Ends: 31-Dec-2025
1,381,000
할인액 207,000 (15%)
Each
카트에 추가하기
The Click-iT™ TUNEL Colorimetric IHC Detection Kit is used to identify apoptotic cells in tissue and cultured cell samples through the use of a small, highly specific labeling moiety and streptavidin-peroxidase conjugation. After incorporation of the labeling moiety into sites of DNA fragmentation, detection is achieved through a catalyzed 'click' reaction that adds a biotin group at these sites. The subsequent addition of a streptavidin-peroxidase and peroxidase substrate results in a dark brown signal that can be detected with light microscopy and stored for future analysis.

Find more tools for image-based detection of apoptotic cells >

• Optimized for the detection of apoptotic cells in either tissue or cell samples
• Improved colorimetric TUNEL assay—better label incorporation due to small reactive moiety
• Increased sensitivity—specific label incorporation results in lower background and brighter signal
• Content-rich results—cell morphology, cellular environment, and apoptotic signal are clearly visible
• Flexibility—the assay can be configured for 50 independent TUNEL apoptosis tests

The later stages of apoptosis are characterized by changes in nuclear morphology, chromatin condensation, nuclear envelope degradation, and DNA fragmentation. Terminal deoxynucleotidyl transferase-dUTP nick end labeling (TUNEL) assays are based on the incorporation of modified dUTPs by terminal deoxynucleotidyl transferase (TdT) at the 3’-OH ends of fragmented DNA. Colorimetric TUNEL assays utilize dUTPs conjugated with a biotin moiety, followed by the addition of a streptavidin-peroxidase conjugate and peroxidase substrate, resulting in a dark brown apoptotic signal. However, colorimetric TUNEL assays are prone to high background, which reduces the sensitivity and specificity of the signal.

The Click-iT TUNEL Colorimetric IHC Detection Kit was developed to address these issues by utilizing a dUTP modified with an alkyne group (a small bio-orthogonal functional group) that enables the nucleotide to be more readily incorporated by TdT. After incorporation, a highly specific click reaction covalently links biotin azide and the alkyne group. Streptavidin-peroxidase (horseradish peroxidase) followed by peroxidase substrate (DAB) are added, allowing colorimetric detection of apoptotic cells. The high degree of labeling specificity inherent in the click technology results in low background and improved detection of apoptotic cells.

The Click-iT TUNEL Colorimetric IHC Detection Kit has been optimized and contains all of the reagents needed for detection of apoptotic cells from either tissue or cell samples. The reagents supplied in this kit can be used to test 50 samples and configured to test from one to 50 samples at a time.
For Research Use Only. Not for use in diagnostic procedures.
사양
용도(장비)EVOS™ XL Core Imaging System, EVOS™ XL Imaging System
제품라인Click-iT
제품 유형TUNEL Colorimetric IHC Detection Kit
수량1 Kit
배송 조건Dry Ice
검출 방법Colorimetric
형식Slide
Unit SizeEach
구성 및 보관
Mixed storage conditions for kit components: 2–8°C and -5 to -30°C

자주 묻는 질문(FAQ)

Can Metal Enhanced DAB Substrate Kit (Cat No. 34065) be used instead of the DAB provided in the Click-iT TUNEL Colorimetric IHC Detection Kit?

Yes, but we have not optimized its use with this kit.

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

Can the Click-iT TUNEL Colorimetric IHC Detection Kit be used with other colorimetric dyes?

Yes, other colorimetric stains can be used.

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

I ran out of the TdT enzyme used in the Click-iT TUNEL assay. Can I purchase it separately?

Yes, additional Terminal Deoxynucleotidyl Transferase (rTdT) can be purchased as Cat. No. 10533-065 or 10533-075. Additional TdT reaction buffer can be purchased as Cat. No. 16314-015.

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

Can I perform Click-iT EdU TUNEL detection on cells growing in 3D culture?

We have not validated the use of EdU TUNEL for apoptosis detection in 3D culture systems, but as this reagent is compatible for labeling cells in vivo, it is also expected to label cells in 3D culture systems. There are a number of reports in the literature that use this product in 3D culture systems; here are some citations:

Lei Y, Schaffer DV (2013) A fully defined and scalable 3D culture system for human pluripotent stem cell expansion and differentiation. Proc Natl Acad Sci U S A 110:E5039-E5048.
Derda R, Laromaine A, Mammoto A et al. (2009) Paper-supported 3D cell culture for tissue-based bioassays. Proc Natl Acad Sci U S A 106:18457-18462.
Robertson FM, Ogasawara MA, Ye Z et al. (2010) Imaging and Analysis of 3D Tumor Spheroids Enriched for a Cancer Stem Cell Phenotype. J Biomol Screen 15:820-829.

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

For the Click-iT TUNEL for In Situ Apoptosis Detection Assay, how long should I digest my tissue samples in proteinase K?

Most tissue samples will be adequately digested in 15 minutes. The optimal incubation time will vary depending on tissue type and thickness. We have observed that brain tissue needs longer proteinase K treatment than other tissues tested.

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

인용 및 참조 문헌 (13)

인용 및 참조 문헌
Abstract
Usp9X Regulates Cell Death in Malignant Peripheral Nerve Sheath Tumors.
Authors:Bianchetti E, Bates SJ, Carroll SL, Siegelin MD, Roth KA,
Journal:Sci Rep
PubMed ID:30478285
'Malignant peripheral nerve sheath tumors (MPNSTs) are the leading cause of death in neurofibromatosis type 1 (NF1) patients. Current treatment modalities have been largely unsuccessful in improving MPNST patient survival, making the identification of new therapeutic targets urgent. In this study, we found that interference with Usp9X, a deubiquitinating enzyme ... More
Inhibition of Hedgehog signaling reprograms the dysfunctional immune microenvironment in breast cancer.
Authors:Hanna A, Metge BJ, Bailey SK, Chen D, Chandrashekar DS, Varambally S, Samant RS, Shevde LA,
Journal:Oncoimmunology
PubMed ID:30723576
'Host responses to tumor cells include tumor suppressing or promoting mechanisms. We sought to detail the effect of Hedgehog (Hh) pathway inhibition on the composition of the mammary tumor immune portfolio. We hypothesized that Hh signaling mediates a crosstalk between breast cancer cells and macrophages that dictates alternative polarization of ... More
The structural atrophy of the aneurysm wall in secondary expanding aortic aneurysms with endoleak type II.
Authors:Menges AL, Busch A, Reutersberg B, Trenner M, Kath P, Chernogubova E, Maegdefessel L, Eckstein HH, Zimmermann A
Journal:J Vasc Surg
PubMed ID:30792063
'Abdominal aortic aneurysm (AAA) has an age-dependent prevalence of 2% to 11% and is a leading cause of death in men aged >65 years if not treated surgically. Today, endovascular aneurysm repair (EVAR) is performed in up to 80% of elective cases and 60% of ruptured cases. Although EVAR improves perioperative, ... More
Anti-tumor effect of cisplatin in human oral squamous cell carcinoma was enhanced by andrographolide via upregulation of phospho-p53 in vitro and in vivo.
Authors:Chen S, Hu H, Miao S, Zheng J, Xie Z, Zhao H,
Journal:Tumour Biol
PubMed ID:28513299
'Oral squamous cell carcinoma is one of the most common neoplasm in the world. Despite the improvements in diagnosis and treatment, the outcome is still poor now. Thus, the development of novel therapeuticapproaches is needed. The aim of this study is to assess the synergistic anti-tumor effect of andrographolide with ... More
Synergistic anti-tumor efficacy of sorafenib and fluvastatin in hepatocellular carcinoma.
Authors:Cheng Y, Luo R, Zheng H, Wang B, Liu Y, Liu D, Chen J, Xu W, Li A, Zhu Y,
Journal:Oncotarget
PubMed ID:28423574
Drug resistance to sorafenib is common in patients with hepatocellular carcinoma(HCC). We examined the effects of a combination of sorafenib and fluvastatin on HCC using in vitro and in vivo models. The dual treatment induced apoptosis and reduced cellular viability in HCC more effectively than either drug alone. The combination ... More