Date published: 2025-11-22

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K-562 nuclear extract: sc-2130

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Datasheets
  • supplied in four vials, each containing 250 µg nuclear extract in 50 µl buffer
  • provided in 20 mM HEPES (pH 7.9), 20% v/v glycerol, 0.1 M KCI, 0.2 mM EDTA, 0.5 mM PMSF and 0.5 mM DTT
  • human nuclear extract; chronic myelogenous leukemia cells
  • suitable for use in Gel Shift and Western Blotting assays
  • Extracts should be stored at -70°C and repeated freezing and thawing should be avoided.
  • prepared by the method of Dignam et al., (1983) Nucleic Acids Res. 11: 1475

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K-562 nuclear extract is derived from the K-562 cell line, originally established from a patient with chronic myeloid leukemia and extensively used in research to study hematopoietic and leukemic cell processes. This nuclear extract contains a concentrated array of nuclear proteins, including transcription factors, RNA polymerase, and other regulatory molecules crucial for studying gene expression and signal transduction within leukemic cells. Researchers employ K-562 nuclear extract primarily for its utility in investigating mechanisms of gene regulation involved in cell proliferation and survival. The extract is particularly valuable in chromatin immunoprecipitation (ChIP) assays, where it aids in identifying the interaction sites of specific transcription factors on DNA, as well as in electrophoretic mobility shift assays (EMSA) to study the binding dynamics of nuclear proteins to DNA. These applications allow for a deeper understanding of the transcriptional control mechanisms that are active in hematopoietic malignancies. Additionally, the extract is used to examine the effects of various biochemical modulators on the nuclear components of leukemic cells, thus contributing to fundamental insights into cellular regulation and signaling pathways. The origin and consistency of the K-562 cell line are rigorously verified, ensuring that the extract remains a reliable and relevant tool for basic biological research.

K-562 nuclear extract References:

  1. A common functional C-T substitution polymorphism in the promoter region of the human catalase gene influences transcription factor binding, reporter gene transcription and is correlated to blood catalase levels.  |  Forsberg, L., et al. 2001. Free Radic Biol Med. 30: 500-5. PMID: 11182520
  2. Regulation of FeLV-945 by c-Myb binding and CBP recruitment to the LTR.  |  Finstad, SL., et al. 2004. Virol J. 1: 3. PMID: 15507152
  3. Dietary docosahexaenoic acid suppresses T cell protein kinase C theta lipid raft recruitment and IL-2 production.  |  Fan, YY., et al. 2004. J Immunol. 173: 6151-60. PMID: 15528352
  4. MyD88, IRAK1 and TRAF6 knockdown in human chondrocytes inhibits interleukin-1-induced matrix metalloproteinase-13 gene expression and promoter activity by impairing MAP kinase activation.  |  Ahmad, R., et al. 2007. Cell Signal. 19: 2549-57. PMID: 17905570
  5. Protein-DNA interactions in vivo of an erythroid-specific, human beta-globin locus enhancer.  |  Reddy, PM. and Shen, CK. 1991. Proc Natl Acad Sci U S A. 88: 8676-80. PMID: 1924329
  6. Dietary curcumin and limonin suppress CD4+ T-cell proliferation and interleukin-2 production in mice.  |  Kim, W., et al. 2009. J Nutr. 139: 1042-8. PMID: 19321585
  7. Effects of butyltin exposures on MAP kinase-dependent transcription regulators in human natural killer cells.  |  Person, RJ. and Whalen, MM. 2010. Toxicol Mech Methods. 20: 227-33. PMID: 20370538
  8. The effect of nano-silver on the activation of nasal polyp epithelial cells by Alternaria, Der P1 and staphylococcal enterotoxin B.  |  Shin, SH. and Ye, MK. 2011. Int Immunopharmacol. 11: 1691-6. PMID: 21683166
  9. Bee venom at different concentrations modulates the aeroallergen-induced activation of nasal polyp epithelial cells.  |  Shin, SH., et al. 2013. Pharmacology. 91: 39-47. PMID: 23154617
  10. Activation of transcription factors in a mouse lung following exposure to environmental chemical and biological agents.  |  Win-Shwe, TT. and Fujimaki, H. 2015. J Toxicol Sci. 40: 559-68. PMID: 26354372
  11. miR-146a targeted to splenic macrophages prevents sepsis-induced multiple organ injury.  |  Funahashi, Y., et al. 2019. Lab Invest. 99: 1130-1142. PMID: 30700845
  12. Identification of an upstream enhancer containing an AML1 site in the human myeloperoxidase (MPO) gene.  |  Austin, GE., et al. 1998. Leuk Res. 22: 1037-48. PMID: 9783807

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

K-562 nuclear extract

sc-2130
250 µg/0.05 ml
$160.00