By Thomas S.K. Wan (eds.)
This quantity presents readers with specific protocols masking the most melanoma cytogenetics innovations wanted for scientific usage and examine reasons. The chapters during this e-book hide subject matters comparable to chromosome training for myeloid malignancies; chromosome bandings; fluorescence in situ hybridization probe education; array-based comparative genomic hybridization; and cytogenetic nomenclature and reporting. The up-to-date studies on chromosomal abnormalities in hematological malignancies are very good publications for cytogenetics information interpretations and particular malignant illnesses correlation. Written within the hugely winning Methods in Molecular Biology series structure, chapters contain introductions to their respective subject matters, lists of the mandatory fabrics and reagents, step by step, with no trouble reproducible laboratory protocols, and tips about troubleshooting and keeping off identified pitfalls.
Cutting-edge and complete, Cancer Cytogenetics: equipment and Protocols is a helpful source for the beginner in cytogenetics since it offers invaluable guiding protocols, yet it’s additionally nice when you are already engaged within the box and are trying to find a few technical hints.
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Additional resources for Cancer Cytogenetics: Methods and Protocols
Add enough per mL) MarrowMax Bone Marrow Medium to C1 and RTU-RPMI to C2 so that the final volume is 5 mL. 5, step 3 15–30 cells Set up two tubes. Remove one half of the volume in C1 and add to another flat-sided culture tube labeled C2. Add enough MarrowMax Bone Marrow Medium to C1 and RTU-RPMI to C2 so that the final volume is 10 mL. 5, step 3 30–50 cells Set up four tubes. 25 × 106 C3, C4. Add enough MarrowMax Bone Marrow Medium to C1 cells per mL) and RTU-RPMI to tubes C2, C3, and C4 so that the final volume is 10 mL.
2 for cell washing. 10. 8). Filter before use. 11. Light microscope with phase-contrast illuminator and equipped with 10× (phase contrast), 40× (phase contrast), and 50× (brightfield–dry) objectives (see Note 3). 12. 100-mL glass Coplin jars. 3 Methods Perform in a class II safety cabinet due to aerosol and cross infection risks issues. 1 Sample Types Clinical samples may be for diagnostics or research. For research purposes, separate informed patient consent must be obtained in advance and ethical approval documented in accordance with local regulations.
Bottlenecking Chromosome Preparation of Cancer Cells 49 selection along with cross-contamination may contribute significantly to reports of “genetic instability”—a charge sometimes laid unjustly at the door of cell lines. 4 2 Cell Culture For the advice on cancer cell culture, including the choice of laminar flow safety cabinets and incubators, readers are urged to consult one of the many available specialist works now available [9, 10]. The most critical component of cell culture systems is probably the fetal bovine serum (FBS), which is normally added at 10–20 % unless otherwise specified.
Cancer Cytogenetics: Methods and Protocols by Thomas S.K. Wan (eds.)