WB, ELISA, ICC/IF, IHC, IHC-PHost:
Hu, Mu, RtApplications:
WB, Simple Western, CyTOF-ready, ICC, ICFlowHost:
Hu, Mu, Rt, MkApplications:
WB, ICC/IF, IHC, IHC-Fr, IHC-PHost:
Applications: WB, IP
Applications: WB, DB, ELISA, IHC, IHC-P
Albumin is a soluble, monomeric protein which comprises about one half of the blood serum protein. Albumin functions primarily as a carrier protein for steroids, fatty acids, and thyroid hormones and plays a role in stabilizing extracellular fluid volume. Mutations in this gene on chromosome 4 result in various anomalous proteins. Albumin is a globular unglycosylated serum protein of molecular weight 65,000. The human albumin gene is 16,961 nucleotides long from the putative 'cap' site to the first poly(A) addition site. It is split into 15 exons which are symmetrically placed within the 3 domains that are thought to have arisen by triplication of a single primordial domain. Albumin is synthesized in the liver as preproalbumin which has an N terminal peptide that is removed before the nascent protein is released from the rough endoplasmic reticulum. The product, proalbumin, is in turn cleaved in the Golgi vesicles to produce the secreted albumin.
Bioinformatics Tool for Albumin
Discover related pathways, diseases and genes to Albumin. Need help? Read the Bioinformatics Tool Guide
for instructions on using this tool.
Related Albumin Blog Posts
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|Albumin - a family of globular protein
Albumin is a soluble and globular monomeric protein encoded by chromosome 4 that comprises about half of the protein found in blood serum. It functions as a carrier protein for steroids, fatty acids, and thyroid hormones as well as stabilizing extrace... Read more.