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Flow Cytometric Analysis of Notch4 expression on a human lymphoblastic leukemia cell line. Human MOLT-3 lymphoblastic leukemia cells (ATCC, CRL-1552™) were harvested and stained with either PE Mouse IgG1, κ Isotype Control (Cat. No. 554680; dashed line histogram) or PE Mouse Anti-Human Notch4 antibody (solid line histogram) at matched concentrations. The fluorescence histograms were derived from gated events based on the forward and side light scattering characteristics of viable MOLT-3 cells. Flow cytometric analysis was performed using a BD FACSCanto™ II Flow Cytometry System.
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BD Pharmingen™ PE Mouse Anti-Human Notch4
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- This reagent has been pre-diluted for use at the recommended Volume per Test. We typically use 1 × 10^6 cells in a 100-µl experimental sample (a test).
- An isotype control should be used at the same concentration as the antibody of interest.
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The MHN4-2 monoclonal antibody specifically binds to an extracellular domain of Neurogenic locus notch homolog protein 4, also known as, Notch4 (or Notch 4 and Notch-4). Notch4 is a type 1 transmembrane glycoprotein that belongs to the Notch Receptor Family comprised of Notch1 through Notch4. Notch4 serves as a receptor for several ligands including Delta1, Jagged1, and Jagged2 that can be expressed on the same or different cells. Notch4 plays important roles in embryonic and postnatal development and cell fate determination by regulating cellular differentiation, proliferation and apoptosis. After ligand binding, the Notch4 receptor is cleaved in its extracellular and transmembrane domains. The cleaved notch intracellular domain (NICD) dissociates from the membrane and translocates to the nucleus where it can act as a transcriptional activator of downstream target genes involved with cellular differentiation and other responses. Notch4 is expressed at high levels in the heart and by endothelial cells and by certain CD34-positive and CD34-negative human bone marrow cell subsets. It is over-expressed by cells in certain breast, colon, and lung cancers.

Development References (8)
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Harrison H, Farnie G, Howell SJ, et al. Regulation of breast cancer stem cell activity by signaling through the Notch4 receptor. Cancer Res. 2010; 70(2):709-718. (Biology). View Reference
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Karanu FN, Yuefei L, Gallacher L, Sakano S, Bhatia M. Differential response of primitive human CD34- and CD34+ hematopoietic cells to the Notch ligand Jagged-1. Leukemia. 2003; 17(7):1366-1374. (Biology). View Reference
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Li L, Huang GM, Banta AB, et al. Cloning, characterization, and the complete 56.8-kilobase DNA sequence of the human NOTCH4 gene. Genomics. 1998; 51:45-58. (Biology). View Reference
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Sekine C, Koyanagi A, Koyama N, Hozumi K, Chiba S, Yagita H. Differential regulation of osteoclastogenesis by Notch2/Delta-like 1 and Notch1/Jagged1 axes. Arthritis Res Ther. 2012; 14(2):R45-R58. (Immunogen: Flow cytometry, Functional assay). View Reference
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Sugaya K, Sasanuma S, Nohata J, et al. Gene organization of human NOTCH4 and (CTG)n polymorphism in this human counterpart gene of mouse proto-oncogene Int3. Gene. 1997; 189(2):235-244. (Biology). View Reference
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Sun Y, Lowther W, Kato K, et al. Notch4 intracellular domain binding to Smad3 and inhibition of the TGF-beta signaling. Oncogene. 2005; 24(34):5365-5374. (Biology). View Reference
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Vercauteren SM, Sutherland HJ. Constitutively active Notch4 promotes early human hematopoietic progenitor cell maintenance while inhibiting differentiation and causes lymphoid abnormalities in vivo. Blood. 2004; 104(8):2315-2322. (Biology). View Reference
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Wu J, Iwata F, Grass JA, et al. Molecular determinants of NOTCH4 transcription in vascular endothelium. Mol Cell Biol. 2005; 25(4):1458-1474. (Biology). View Reference
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For Research Use Only. Not for use in diagnostic or therapeutic procedures.