Date published: 2025-10-14

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U-2 OS Cell Lysate: sc-2295

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Datasheets
  • 500 µg protein in 200 µl SDS-PAGE Western blotting buffer
  • human whole cell lysate; osteogenic sarcoma cells
  • whole cell lysate provided as Western blotting positive control
  • should be stored at -20°C and repeated freezing and thawing should be minimized
  • sample vial should be placed at 95° C for up to 5 minutes, once prior to use

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    U-2 OS is a cell line derived from from a sarcoma of the tibia of a 15-year-old, female osteosarcoma patient. This lysate is extensively used in cancer research to study the molecular mechanisms underlying osteosarcoma, a type of bone cancer. U-2 OS cells exhibit characteristic genetic and epigenetic alterations, including mutations in the TP53 gene and overexpression of oncogenes such as c-Myc, making the lysate valuable for analyzing signaling pathways involved in tumor growth, survival, and metastasis. Researchers utilize U-2 OS Cell Lysate to investigate the expression, phosphorylation, and interaction of key proteins involved in pathways like PI3K/AKT, Wnt/β-catenin, and MAPK/ERK using techniques such as western blotting, immunoprecipitation, and mass spectrometry. This lysate aids in exploring the molecular basis of osteosarcoma cell proliferation, migration, and invasion by examining the roles of cell cycle regulators, matrix metalloproteinases, and adhesion molecules. Additionally, U-2 OS Cell Lysate is employed to study the effects of various chemical compounds on these signaling pathways, providing insights into the cellular processes that drive osteosarcoma progression. By comparing U-2 OS lysates with those from normal osteoblasts, scientists can identify specific molecular alterations associated with osteosarcoma, advancing research in cancer biology and signal transduction.

    U-2 OS Cell Lysate References:

    1. Distinct phosphorylation events regulate p130- and p107-mediated repression of E2F-4.  |  Farkas, T., et al. 2002. J Biol Chem. 277: 26741-52. PMID: 12006580
    2. Detection and identification of transcription factors as interaction partners of alien in vivo.  |  Kob, R., et al. 2007. Cell Cycle. 6: 993-6. PMID: 17438371
    3. Kinobead and Single-Shot LC-MS Profiling Identifies Selective PKD Inhibitors.  |  Golkowski, M., et al. 2017. J Proteome Res. 16: 1216-1227. PMID: 28102076
    4. Affimer proteins are versatile and renewable affinity reagents.  |  Tiede, C., et al. 2017. Elife. 6: PMID: 28654419
    5. Identification of novel PANDAR protein interaction partners involved in splicing regulation.  |  Pospiech, N., et al. 2018. Sci Rep. 8: 2798. PMID: 29434205
    6. Non-Steric Interactions Predict the Trend and Steric Interactions the Offset of Protein Stability in Cells.  |  Davis, CM. and Gruebele, M. 2018. Chemphyschem. 19: 2290-2294. PMID: 29877016
    7. Combined Proteomic and In Silico Target Identification Reveal a Role for 5-Lipoxygenase in Developmental Signaling Pathways.  |  Brand, S., et al. 2018. Cell Chem Biol. 25: 1095-1106.e23. PMID: 30251630
    8. Cellular Sticking Can Strongly Reduce Complex Binding by Speeding Dissociation.  |  Davis, CM. and Gruebele, M. 2021. J Phys Chem B. 125: 3815-3823. PMID: 33826329
    9. Cooperation of Stat2 and p300/CBP in signalling induced by interferon-alpha.  |  Bhattacharya, S., et al. 1996. Nature. 383: 344-7. PMID: 8848048

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    U-2 OS Cell Lysate

    sc-2295
    500 µg/200 µl
    $118.00