Il existe 5+ publications pour ce produit.
L’anticorps anti-Disialoganglioside GD3 Monoclonal Souris est utilisé pour la détection de Disialoganglioside GD3 dans des échantillons de Humain. Il a été validé pour CyTox, IHC (fro), FACS et IF.
Gangliosides are sialic-acid bearing glycolipids expressed on the surface of all mammalian cells, and are likely involved in mediating cell-substratum interactions. They are important target antigens for antibody mediated cytolysis of human melanoma and neuroblastoma cells. Human melanoma cells produce gangliosides GD2 and/or GD3 which are present in substratum-attached material, and may play a significant role in the melanoma metastatic phenotype. Ganglioside GD3 is a major surface marker on most human melanoma cells. MB3.6 has been used to localize GD3 in the plasma membrane and in focal adhesion plaques of human melanoma cells.
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Store undiluted at 4°C.
Mujoo, Cheresh, Yang, Reisfeld: "Disialoganglioside GD2 on human neuroblastoma cells: target antigen for monoclonal antibody-mediated cytolysis and suppression of tumor growth." dans: Cancer research, Vol. 47, Issue 4, pp. 1098-104, (1987) (PubMed).
Cheresh, Pierschbacher, Herzig, Mujoo: "Disialogangliosides GD2 and GD3 are involved in the attachment of human melanoma and neuroblastoma cells to extracellular matrix proteins." dans: The Journal of cell biology, Vol. 102, Issue 3, pp. 688-96, (1986) (PubMed).
Cheresh, Honsik, Staffileno, Jung, Reisfeld: "Disialoganglioside GD3 on human melanoma serves as a relevant target antigen for monoclonal antibody-mediated tumor cytolysis." dans: Proceedings of the National Academy of Sciences of the United States of America, Vol. 82, Issue 15, pp. 5155-9, (1985) (PubMed).
Hakomori: "Tumor-associated carbohydrate antigens." dans: Annual review of immunology, Vol. 2, pp. 103-26, (1985) (PubMed).
Cheresh, Harper, Schulz, Reisfeld: "Localization of the gangliosides GD2 and GD3 in adhesion plaques and on the surface of human melanoma cells." dans: Proceedings of the National Academy of Sciences of the United States of America, Vol. 81, Issue 18, pp. 5767-71, (1984) (PubMed).