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Titlebook: Metastasis Research Protocols; Susan A. Brooks,Udo Schumacher Book 20011st edition Humana Press 2001 Grading.angiogenesis.cells.migration.

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Surrogate Markers of Angiogenesis and Metastasishe most widely used method to assess angiogenesis is quantification of intratumoral microvessel density (IMD) of the primary tumor by using specific markers for endothelial cells such as factor VIII-related antigen (FVIII-RA), anti-CD31 (platelet endothelial cell adhesion molecule, PECAM), or anti-C
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Assessment of Cellular Proliferation by Calculation of Mitotic Index and by Immunohistochemistrya) or even a variation in non-neoplastic elements such as fibrotic tissue. For many years microscopists used the number of mitotic figures present in a tissue section to estimate how rapidly the cells are proliferating and thereby gauge how aggressive the tumor was likely to be. With a few refinemen
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SDS -PAGE and Western Blotting Techniquesnt for obtaining accurate separation of the proteins on the basis of molecular weight. Depending on whether an antigen is primarily extracellular, cytoplasmic, or membrane-associated different procedures might be required to prepare the sample initially. Although there are exceptions, many soluble n
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Hybridization to Localize mRNAsducible and easily interpretable results without the need to adjust the method to individual cell types within sections. For alternative methodology for fluorescent in situ hybridization (FISH) techniques, please refer to . by Goker and Shipley. The protocol described here gives good results for the
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Fluorescence itIn Situ Hybridizationed (3-7). The ease and effectiveness of fluorescence methods (fluorescence in situ hybridization [FISH]) in particular have now almost rendered the radioisotopic techniques obsolete. FISH has been developed to incorporate chromosome painting and the analysis of the whole genome for aberrations using
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Book 20011st editionized approaches and specific examples of their application, because—although the methodology is readily available in the published literature and established in many laboratories—we wished these volumes to “stand alone” and to make accessible here the standard techniques that underpin much metastasi
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