Senescence β-Galactosidase Staining Kit #9860
Product Information
Protocol
Product Description
The Senescence β-Galactosidase Staining Kit is designed to conveniently provide reagents needed to detect β-galactosidase activity at pH 6, a known characteristic of senescent cells. Papers have published using this kit in both cells and frozen tissue. The kit includes all reagents necessary for this assay.
Background
Limited capacity to replicate is a defining characteristic of most normal cells and culminates in senescence, an arrested state in which the cell remains viable (1). Senescent cells are not stimulated to divide by serum or passage in culture, and senescence invokes a specific cell cycle profile that differs from most damage-induced arrest processes or contact inhibition (2). An enlarged cell size, expression of pH-dependent β-galactosidase activity (3), and an altered pattern of gene expression (4,5) further characterize senescent cells.
- Goldstein, S. (1990) Science 249, 1129-33.
- Sherwood, S. W. et al. (1988) Proc. Natl. Acad. Sci., USA 85, 9086-90.
- Dimri, G. et al. (1995) Proc. Natl. Acad. Sci., USA 92, 9363-7.
- Cristofalo, V. J. et al. (1998) Crit. Rev. Eukaryot Gene Expr. 8, 43-80.
- Linskens, M. H. et al. (1995) Nucleic Acid Res. 23, 3244-51.
Product Citations: 63
- Baker, D. J. et al. (2004) Nat. Genetics 36, 744-749.
- Su, D. et al. (2009) J Biol Chem 284, 12153-64.
- Swarbrick, A. et al. (2008) Proc Natl Acad Sci U S A 105, 5402-7.
- Efeyan, A. et al. (2007) Cancer Res 67, 7350-7.
- Boucher, M.J. et al. (2004) Am J Physiol Gastrointest Liver Physiol 286, G736-46.
- Efeyan, A. et al. (2009) PLoS One 4, e5475.
- Chang, C.J. et al. (2011) Nat Cell Biol 13, 317-23.
- Delmore, J.E. et al. (2011) Cell 146, 904-17.
- Blasco, R.B. et al. (2011) Cancer Cell 19, 652-63.
- Cronin, J.C. et al. (2013) Cancer Res 73, 5709-18.
- Pérez de Castro, I. et al. (2013) Cancer Res 73, 6804-15.
- Wang, M. et al. (2014) Cancer Res 74, 2825-34.
- Park, E. et al. (2013) Mol Cell 50, 908-18.
- Rader, J. et al. (2013) Clin Cancer Res 19, 6173-82.
- Guo, J.Y. et al. (2013) Genes Dev 27, 1447-61.
- Evangelou, K. et al. (2013) Cell Death Differ 20, 1485-97.
- Khongkow, P. et al. (2014) Oncogene 33, 4144-55.
- Flach, J. et al. (2014) Nature 512, 198-202.
- Tang, Y. et al. (2013) Oncogene 32, 2792-8.
- Agrelo, R. et al. (2013) Oncogene 32, 5492-500.
- Li, Z. et al. (2013) Oncotarget 4, 2532-49.
- Gagou, M.E. et al. (2014) Oncotarget 5, 11381-98.
- Zhou, Z.W. et al. (2013) PLoS Genet 9, e1003702.
- Sanchez, N. et al. (2013) PLoS One 8, e65671.
- Li, L.H. et al. (2014) PLoS One 9, e104203.
- Arason, A.J. et al. (2014) PLoS One 9, e88683.
- Krencik, R. et al. (2015) Sci Transl Med 7, 286ra66.
- Kovatcheva, M. et al. (2015) Oncotarget 6, 8226-43.
- Chen, R. et al. (2015) Oncotarget 6, 32841-55.
- Kannan, A. et al. (2016) Oncotarget 7, 6576-92.
- Havel, J.J. et al. (2015) Oncogene 34, 1487-98.
- Defamie, V. et al. (2015) Oncogene 34, 4098-108.
- Khongkow, P. et al. (2016) Oncogene 35, 990-1002.
- Castillo-Lluva, S. et al. (2015) Oncogene 34, 4777-90.
- Wan, Y. et al. (2015) J Cell Biol 209, 235-46.
- Yuan, Y. et al. (2016) J Biol Chem 291, 1307-19.
- Gabitova, L. et al. (2015) Cell Rep 12, 1927-38.
- Solovjeva, L. et al. (2015) BMC Mol Biol 16, 18.
- Chung, S.I. et al. (2016) Oncotarget 7, 7354-66.
- Lowe, D. et al. (2016) Oncotarget 7, 8524-31.
- Lee, H. et al. (2016) Oncotarget 7, 19134-46.
- Chang, J. et al. (2016) Nat Med 22, 78-83.
- Baker, D.J. et al. (2016) Nature 530, 184-9.
- Takai, H. et al. (2016) Genes Dev 30, 812-26.
- Borghesan, M. et al. (2016) Cancer Res 76, 594-606.
- De Amicis, F. et al. (2016) Oncotarget , 57955-57969.
- Oh, A.Y. et al. (2016) Cancer Res 76, 4791-804.
- Lawson, C.D. et al. (2016) Cancer Res 76, 3826-37.
- Liceras-Boillos, P. et al. (2016) Oncogene , .
- Sriraman, A. et al. (2016) Oncotarget 7, 31623-38.
- Lee, H. et al. (2016) Oncotarget 7, 19134-46.
- Lowe, D. et al. (2016) Oncotarget 7, 8524-31.
- Borghesan, M. et al. (2016) Cancer Res 76, 594-606.
- Yuan, Y. et al. (2016) J Biol Chem 291, 1307-19.
- Kannan, A. et al. (2016) Oncotarget 7, 6576-92.
- Shao, Z. et al. (2016) Nat Commun 7, 10869.
- Xiong, Z.M. et al. (2016) Aging Cell 15, 279-90.
- Soriano-Arroquia, A. et al. (2016) Aging Cell 15, 361-9.
- Llanos, S. et al. (2016) Nat Commun 7, 10438.
- Walter, D. et al. (2016) Nat Commun 7, 10530.
- Felsenstein, K.M. et al. (2016) ACS Chem Biol 11, 139-48.
- Frame, F.M. et al. (2016) Cancer Med 5, 61-73.
- Zhu, N. et al. (2016) Stem Cells Int 2016, 5687589.
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