Oncogene techniques by Abelson J.N., Simon M.I., Vogt P.K. (eds.)

By Abelson J.N., Simon M.I., Vogt P.K. (eds.)

Normal Description of the Volume:Oncogenes became a principal concentration of melanoma study. All occupied with this self-discipline will locate this quantity a useful reduction in constructing protocols wanted for his or her research.General Description of the Series:The seriously acclaimed laboratory common for greater than 40 years, tools in Enzymology is among the so much hugely revered courses within the box of biochemistry. due to the fact 1955, each one quantity has been eagerly awaited, usually consulted, and praised through researchers and reviewers alike. Now with greater than three hundred volumes (all of them nonetheless in print), the sequence comprises a lot fabric nonetheless appropriate this day - actually an important booklet for researchers in all fields of lifestyles sciences.Key positive aspects• cellphone tradition• Molecular cloning• Gene functionality• Protein-protein interactions• Protein-DNA interactions

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In general, sections from tissues frozen in OCT (Miles, Elkhart, IN) give the best results in immunohistochemistry, although Carnoy's fixative (60% ethanol:30% 9s T. Tennenbaum, S. H. Yuspa, A. Grover, V. Castronovo, M. E. Sobel, Y. Yamada, and L. M. De Luca, Cancer Res. 52, 2966 (1992). '~'~D. R. Roop, C. K. Cheng, L. Titterington, C. A. Meyers, J. R. Stanley, P. M. Steinert, and S. H. Yuspa, J. Biol. Chem. 259, 8037 (1984). m~T. Tennenbaum, A. K. Weiner, A. J. B61anger, A. B. Glick, H. Hennings, and S.

Notario, Cell Growth Differ. 4, 367 (1993). 5aj. I. Lee and L. B. Taichman, J. Invest. Dermatol. 92, 267 (1989). 52R. Neades, N. A. Betz, X. Y. Sheng, and J. C. Pelling, Mol. Carcinog. 4, 369 (1991). 53C. Byrne and E. Fuchs, Mol. Cell. Biol. 13, 3176 (1993). 54C. A. Huff, S. H. Yuspa, and D. Rosenthal, J. Biol. Chem. 268, 377 (1993). 55D. A. Greenhalgh, J. A. Rothnagel, X. J. Wang, M. I. Quintanilla, C. C. Orengo, T. A. Gagne, D. S. Bundman, M. A. Longley, C. Fisher, and D. R. Roop, Oncogene 8, 2145 (1993).

Gage, in "Neural Transplantation" (S. B. Dunnett and A. ), p. 20. Oxford University Press, New York, 1992. 4 ~M aminopterin, and 16 /xM thymidine). The neuroblastoma line is usually grown in DMEM + 10% FBS. 2. Layer hippocampi-PHAP cells on logarithmically growing neuroblastoma cells. After 15 rain, remove the unattached cells by aspiration. Add 50% polyethylene glycol (PEG 1000, KochLight) in DMEM (v/v) to initiate cell fusion. Remove the solution after 40 sec and, after 60 sec, wash cells and incubate the cultures in DMEM + 10% FBS overnight.

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