Cell Meter™ Autophagy Assay Kit *Green Fluorescence*
This Cell Meter™ Autophagy Kit employs Autophagy Green™ as a specific autophagosome marker to analyze the activity of autophagy. The assay is optimized for direct detection of autophagy in both detached and attached cells. The kit provides all the essential components for the assay protocol. Cell Meter™ Autophagy Kit is suitable for fluorescence microscope, fluorescence microplate reader and flow cytometer. Autophagy Green™ has a large Stokes shift. Autophagy is an evolutionarily conserved degradation process that targets long-lived proteins, organelles, and other cytoplasmic components for degradation via the lysosomal pathway. The autophagy pathway is complementary to the action of the ubiquitin-proteasome pathway which typically degrades short-lived proteins. Activation of the autophagy pathway is required for multiple cellular roles, including survival during starvation, the clearance of intracellular components, development, and immunity. In the absence of stress, autophagy serves a house-keeping function, removing damaged organelles and cellular components preventing cytotoxic effects. Decreases and defects in autophagy have been implicated in multiple diseases, for example Huntingtons, Alzheimers, and Parkinsons. In terms of cancer development, autophagy seems to play multiple roles. Decreased or absent expression of certain autophagy proteins, such as Beclin-1 and Bif-1, increases tumor susceptibility in mice while the overexpression of these proteins can repress cancer cell growth. However, autophagy is critical for the survival of cancer cells within the nutrient poor and hypoxic core of solid tumors.
Example protocol
AT A GLANCE
Protocol summary
- Prepare cells with your test compounds
- Add Autophagy Green™ working solution
- Incubate at 37°C for 15 - 60 minutes
- Wash cells with Wash Buffer
- Monitor the fluorescence increase at Ex/Em= 485/530 nm (Cutoff = 515 nm), fluorescence microscope with FITC filter set or flow cytometer with 530/30 nm filter (FITC channel)
Important notes
Thaw all the components at room temperature before starting the experiment.
PREPARATION OF WORKING SOLUTION
Add 20 μL of Autophagy Green™ (Component A) to 10 mL of Stain Buffer (Component B) and mix well to make Autophagy Green™ working solution. Protect from light. Note: 20 μL of 500X Autophagy Green™ (Component A) is enough for one 96-well plate. Note: Aliquot and store unused 500X Autophagy Green™ at < -20ºC. Protect from light and avoid repeated freeze-thaw cycles.
For guidelines on cell sample preparation, please visit
https://www.aatbio.com/resources/guides/cell-sample-preparation.html
SAMPLE EXPERIMENTAL PROTOCOL
- Culture cells to a density optimum for autophagy induction according to your specific induction protocol (about 1-2 × 104 cells/ well/96-well plate). At the same time, culture a non-induced negative control cell population at the same density as the induced population for every labeling condition.
- Remove medium.
- Add 100 µL/well (96-well plate) or 25 µL/well (384-well plate) of Autophagy Green™ working solution into each well.
- Incubate the cells in a 37°C, 5% CO2 incubator for 15 to 60 minutes. Note: The appropriate incubation time depends on the individual cell type and cell concentration used. Optimize the incubation time for each experiment.
- Wash the cells with Wash Buffer (Component C) for 3 - 4 times, then add 100 µL Wash Buffer (Component C) to each well. Note: It is recommended to increase either the labeling concentration or the incubation time to allow the dye to accumulate if the cells do not appear to be sufficiently stained.
- Monitor the fluorescence intensity with a fluorescence microplate reader at Ex/Em = 485/530 nm (Cutoff = 515 nm), a fluorescence microscope with FITC filter set or a flow cytometer with 530/30 nm filter (FITC channel).
Citations
View all 12 citations: Citation Explorer
Neuroprotective activities of sertraline, tiagabine, and bicifadine with autophagy-inducing potentials in a 6-hydroxidopamine-treated Parkinson’s disease cell model
Authors: Lee, Chaemi and Kim, Seong Soon and Bae, Myung Ae and Kim, Seong Hwan
Journal: (2024)
Authors: Lee, Chaemi and Kim, Seong Soon and Bae, Myung Ae and Kim, Seong Hwan
Journal: (2024)
Modification of BCLX pre-mRNA splicing has antitumor efficacy alone or in combination with radiotherapy in human glioblastoma cells
Authors: Dou, Zhihui and Lei, Huiwen and Su, Wei and Zhang, Taotao and Chen, Xiaohua and Yu, Boyi and Zhen, Xiaogang and Si, Jing and Sun, Chao and Zhang, Hong and others,
Journal: Cell Death \& Disease (2024): 160
Authors: Dou, Zhihui and Lei, Huiwen and Su, Wei and Zhang, Taotao and Chen, Xiaohua and Yu, Boyi and Zhen, Xiaogang and Si, Jing and Sun, Chao and Zhang, Hong and others,
Journal: Cell Death \& Disease (2024): 160
YAP promotes the healing of ischemic wounds by reducing ferroptosis in skin fibroblasts through inhibition of ferritinophagy
Authors: Cao, Guoqi and Yin, Siyuan and Ma, Jiaxu and Lu, Yongpan and Song, Ru and Wu, Zhenjie and Liu, Chunyan and Liu, Jian and Wu, Peng and Sun, Rui and others,
Journal: Heliyon (2024)
Authors: Cao, Guoqi and Yin, Siyuan and Ma, Jiaxu and Lu, Yongpan and Song, Ru and Wu, Zhenjie and Liu, Chunyan and Liu, Jian and Wu, Peng and Sun, Rui and others,
Journal: Heliyon (2024)
Mitochondrial-Targeted Antioxidant MitoQ-Mediated Autophagy: A Novel Strategy for Precise Radiation Protection
Authors: Bao, Xingting and Liu, Xiongxiong and Wu, Qingfeng and Ye, Fei and Shi, Zheng and Xu, Dan and Zhang, Jinhua and Dou, Zhihui and Huang, Guomin and Zhang, Hong and others,
Journal: Antioxidants (2023): 453
Authors: Bao, Xingting and Liu, Xiongxiong and Wu, Qingfeng and Ye, Fei and Shi, Zheng and Xu, Dan and Zhang, Jinhua and Dou, Zhihui and Huang, Guomin and Zhang, Hong and others,
Journal: Antioxidants (2023): 453
Sarcopenia-derived exosomal micro-RNA 16-5p disturbs cardio-repair via a pro-apoptotic mechanism in myocardial infarction in mice
Authors: Hayasaka, Taiki and Takehara, Naofumi and Aonuma, Tatsuya and Kano, Kohei and Horiuchi, Kiwamu and Nakagawa, Naoki and Tanaka, Hiroki and Kawabe, Jun-ichi and Hasebe, Naoyuki
Journal: Scientific Reports (2021): 1--14
Authors: Hayasaka, Taiki and Takehara, Naofumi and Aonuma, Tatsuya and Kano, Kohei and Horiuchi, Kiwamu and Nakagawa, Naoki and Tanaka, Hiroki and Kawabe, Jun-ichi and Hasebe, Naoyuki
Journal: Scientific Reports (2021): 1--14
References
View all 28 references: Citation Explorer
beta-Elemene induces apoptosis as well as protective autophagy in human non-small-cell lung cancer A549 cells
Authors: Liu J, Hu XJ, Jin B, Qu XJ, Hou KZ, Liu YP.
Journal: J Pharm Pharmacol (2012): 146
Authors: Liu J, Hu XJ, Jin B, Qu XJ, Hou KZ, Liu YP.
Journal: J Pharm Pharmacol (2012): 146
Tgf-beta1 induces autophagy and promotes apoptosis in renal tubular epithelial cells
Authors: Xu Y, Yang S, Huang J, Ruan S, Zheng Z, Lin J.
Journal: Int J Mol Med. (2012)
Authors: Xu Y, Yang S, Huang J, Ruan S, Zheng Z, Lin J.
Journal: Int J Mol Med. (2012)
High-Throughput Screening for AntiInfluenza A Virus Drugs and Study of the Mechanism of Procyanidin on Influenza A VirusInduced Autophagy
Authors: Dai J, Wang G, Li W, Zhang L, Yang J, Zhao X, Chen X, Xu Y, Li K.
Journal: J Biomol Screen. (2012)
Authors: Dai J, Wang G, Li W, Zhang L, Yang J, Zhao X, Chen X, Xu Y, Li K.
Journal: J Biomol Screen. (2012)
An autophagy inhibitor enhances the inhibition of cell proliferation
Authors: Yao F, Wang G, Wei W, Tu Y, Tong H, Sun S.
Journal: Mol Med Report (2012): 84
Authors: Yao F, Wang G, Wei W, Tu Y, Tong H, Sun S.
Journal: Mol Med Report (2012): 84
Salvianolic acid B inhibits autophagy and protects starving cardiac myocytes
Authors: Han X, Liu JX, Li XZ.
Journal: Acta Pharmacol Sin (2011): 38
Authors: Han X, Liu JX, Li XZ.
Journal: Acta Pharmacol Sin (2011): 38
Page updated on December 11, 2024