User:Joehjoeh/FBS V2
Fetal bovine serum (FBS), or fetal calf serum (FCS), is a widely used serum supplement for animal cell culture. fraction remaining after the natural coagulation of blood, followed by centrifugation to remove any remaining red cells[1]. Fetal bovine serum comes from the blood drawn from a bovine fetus via a closed system of collection at the slaughterhouse. Fetal bovine serum is the most widely used serum-supplement for the in vitro cell culture of eukaryotic cells. This is due to it having a very low level of antibodies and containing more growth factors, allowing for versatility in many different cell culture applications.
The globular protein, bovine serum albumin (BSA), is a major component of fetal bovine serum. The rich variety of proteins in fetal bovine serum maintains cultured cells in a medium in which they can survive, grow, and divide.
Production
[edit]Fetal Bovine serum is a by-product of the meat industry. Fetal bovine serum, as with the vast majority of animal serum used in cell culture, is produced from blood collected at commercial slaughterhouses from cattle bred to supply meat destined for human consumption.
The first stage of the production process for fetal bovine serum is the harvesting of blood from the bovine fetus after the fetus is removed from the slaughtered cow. The blood is collected aseptically into a sterile container or blood bag and then allowed to clot. The normal method of collection is cardiac puncture, where they take a needle and insert in between the ribcage into the heart. This minimizes "the danger of serum contamination with micro-organisms from the fetus itself, and the environment". [1] It is then centrifuged to remove the fibrin clot and the remaining blood cells from the clear yellow (straw) colored serum. The serum is frozen prior to further processing that is necessary to make it suitable for cell culture.
The second stage of processing involves filtration, typically using a filtration chain with the final filtration being triple sterile 0.1 micrometre membrane filters. When processed by a reputable commercial serum supplier, the sterilized fetal bovine serum is subjected to stringent quality control testing and is supplied with a detailed Certificate of Analysis. The certificate gives full test results and information concerning the origin of the serum. Certificates of Analysis vary between commercial suppliers, but each usually includes the following details: filtration statement, country of origin, cell growth performance testing, microbial sterility testing, screening for mycoplasma and virus, endotoxin, haemoglobin, IgG and total protein assays.
Ethics
[edit]Ethical questions have been raised regarding the blood collection process with special emphasis on any potential discomfort caused to the fetus. Respected scientific investigation[1][2] has shown that the loss of blood circulation in the dam (mother animal) results in death within seconds of slaughter and that the fetus will be dead within a few minutes of the slaughter of the dam due to oxygen deprivation. In comparison, fetal bovine blood is collected from the bovine fetus only after the pregnant uterus has been removed from the slaughtered cow which, in a typical commercial slaughterhouse, means a delay of around 20 minutes from the time of slaughter. The time between maternal death and the start of fetal blood harvesting is relatively long and therefore means that there is minimal possibility of brain activity in the fetus at the time of blood harvesting and hence minimal possibility of discomfort. Of course, it is important to balance the ethical concerns surrounding the welfare of the donor animal against the highly significant benefits that the use of fetal bovine serum brings to human and animal health.
Serum use
[edit]Fetal bovine serum is commercially available from many manufacturers, and because cells grown in vitro are highly sensitive, customers usually test specific batches to check for suitability for their specific cell type. When changing from batch to batch it is usual to adapt the cells to the new batch of material, for example, by mixing 50% of the old serum with 50% of the new serum and allowing the cells to acclimatise to the new material.
Serum is stored frozen to preserve the stability of components such as growth factors. When serum is thawed, some precipitation may be seen. This is a normal phenomenon and it does not compromise the quality of serum in any way. The precipitate may be removed by transferring the serum to sterile tubes and centrifuging for 5 minutes at 400 x g.
To limit the amount of precipitation, it is recommended that the serum is thawed in a refrigerator at 2-8˚C. The serum should be regularly mixed during this process. Repeated freeze/thaw cycles should be avoided and it is advisable to dispense the serum into single use aliquots before freezing.
TODO: Freezing medium
Regulation
[edit]Serum produced for use in the biotechnology industry and research sectors is highly regulated. The collection and movement of all animal derived products globally is strictly controlled. Veterinary control of animal derived products largely follows the regulations set by the EU (DG SANCO) and the US (USDA). The current regulation governing the importation of animal by-products into the EU is covered by Regulation (EU) 1069/2009 and and the implementation document Regulation (EU) 142/2011.
FBS is a product collected worldwide with the main collections being centered in the United States, Australia, New Zealand, Canada, Central America, South America and Europe.
Global sales
[edit]Sales of FBS in 2008 were estimated to be 700,000 litres globally.
Major companies that collect and sell FBS globally are members of the ISIA, the International Serum Industry Association. Member companies are listed on the ISIA website. Full contact details are available through this portal and the ISIA is able to answer any questions concerning the collection and use of this important resource.
The International Serum Industry Association was incorporated in June 2006 to self-regulate a previously unstandardized industry. The ISIA Mission Statement states: “ISIA shall establish, promote and assure compliance with uncompromised standards of excellence and ethics in the business practices of the global animal serum and animal derived products supply industry. Our primary focus will be on safety and safe use of serum and animal derived products through proper origin traceability, truth in labeling and appropriate standardization and oversight.”[3]
See also
[edit]Blood Plasma Clotting factors Bovine Viruses
External links
[edit]This is where the blood template was
References
[edit]van der valk 03 http://igitur-archive.library.uu.nl/vet/2006-0816-200033/valk_04_thehumanecollection.pdf might have other good refs http://goodcellculture.com/media/documents/Altex20_275_2003.pdf van der valk 10 intro is pretty good http://igitur-archive.library.uu.nl/vet/2011-0111-154938/TIV2364.pdf
"numerous cell line vendors recommend using fbs in cell culture"
- ^ a b c Jochems, Carlo (April-March 2002). "The Use of Fetal Bovine Serum: Ethical or Scientific Problem?". Fund for the Replacement of Animals in Medical Experiments. 30 (2): 219–227. Retrieved 24 April 2012.
{{cite journal}}: Check date values in:|date=(help); Unknown parameter|coauthors=ignored (|author=suggested) (help)CS1 maint: date and year (link) - ^ Mellor DJ, Gregory NG (2003). "Responsiveness, behavioural arousal and awareness in fetal and newborn lambs: experimental, practical and therapeutic implications". N Z Vet J. 51 (1): 2–13. doi:10.1080/00480169.2003.36323. PMID 16032283.
- ^ "Serum Industry". Retrieved 22 February 2013.