Editing Cell biology (section)

== Techniques ==
Cell biology research looks at different ways to culture and manipulate cells outside of a living body to further research in [[human anatomy]] and [[physiology]], and to derive medications. The techniques by which cells are studied have evolved. Due to advancements in microscopy, techniques and technology have allowed scientists to hold a better understanding of the structure and function of cells. Many techniques commonly used to study cell biology are listed below:<ref>{{cite book|title=Cell and Molecular Biology|last1=Lavanya|first1=P.|date=Dec 1, 2005|publisher=Rastogi Publications|isbn=978-8171338177|page=11}}</ref>
* [[Cell culture]]: Utilizes rapidly growing cells on media which allows for a large amount of a specific cell type and an efficient way to study cells.<ref name=":12">{{Cite journal|last=Cooper|first=Geoffrey M.|date=2000|title=Tools of Cell Biology|url=https://www.ncbi.nlm.nih.gov/books/NBK9941/|journal=The Cell: A Molecular Approach. 2nd Edition}}</ref> Cell culture is one of the major tools used in cellular and molecular biology, providing excellent model systems for studying the normal physiology and biochemistry of cells (e.g., metabolic studies, aging), the effects of drugs and toxic compounds on the cells, and mutagenesis and carcinogenesis. It is also used in drug screening and development, and large scale manufacturing of biological compounds (e.g., vaccines, therapeutic proteins).
* [[Fluorescence microscope|Fluorescence microscopy]]: Fluorescent markers such as [[Green fluorescent protein|GFP]], are used to label a specific component of the cell. Afterwards, a certain light wavelength is used to excite the fluorescent marker which can then be visualized.<ref name=":12" />
* [[Phase-contrast microscopy]]: Uses the optical aspect of light to represent the solid, liquid, and gas-phase changes as brightness differences.<ref name=":12" />
* [[Confocal microscopy]]: Combines fluorescence microscopy with imaging by focusing light and snap shooting instances to form a 3-D image.<ref name=":12" />
* [[Transmission electron microscopy]]: Involves metal staining and the passing of electrons through the cells, which will be deflected upon interaction with metal. This ultimately forms an image of the components being studied.<ref name=":12" />
* [[Cytometry]]: The cells are placed in the machine which uses a beam to scatter the cells based on different aspects and can therefore separate them based on size and content. Cells may also be tagged with GFP-fluorescence and can be separated that way as well.<ref>{{Cite journal|last=McKinnon|first=Katherine M.|date=2018-02-21|title=Flow Cytometry: An Overview|journal=Current Protocols in Immunology|volume=120|issue=1 |pages=5.1.1–5.1.11|doi=10.1002/cpim.40|issn=1934-3671|pmc=5939936|pmid=29512141}}</ref>
* [[Cell fractionation]]: This process requires breaking up the cell using high temperature or sonification followed by [[centrifugation]] to separate the parts of the cell allowing for them to be studied separately.<ref name=":12" />