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GPR99 is a G protein-coupled receptor (GPCR) that was originally identified as a purinergic receptor, P2Y15.1,2 However, it is activated by leukotriene E4 (LTE4; Item No. 20410) in the low nanomolar range and by α-ketoglutarate in the high micromolar range.3,4 It is found in the CNS, kidney, epididymis, and other tissues in the mouse, as well as in human kidney, nasal turbinates, and lung, among other tissues.5,6 GPR99 knockout in mice prevents vascular leakage induced by LTE4 and epithelial cell mucin release in mouse nasal mucosa induced by LTE4 or A. alternata.3 In the kidney, under acid-base stress, it is involved with the regulation of carbonic acid and sodium chloride resorption through activation by α-ketoglutarate.5 GPR99 is also expressed in mouse retina, and axon growth is increased when it is activated by α-ketoglutarate in isolated mouse embryo retinal explants.7 Cayman’s GPR99 (C-Term) Polyclonal Antibody can be used for Western blot and immunohistochemistry (IHC) applications. The antibody recognizes the C-terminus of GPR99 from human samples.
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1. GPR99, a new G protein-
2. GPR80/99, proposed to be the P2Y15 receptor activated by adenosine and AMP, is not a P2Y receptor. Purinergic Signal. 1(1), 67-74 (2004).
3. Identification of GPR99 protein as a potential third cysteinyl leukotriene receptor with a preference for leukotriene E4 ligand. The Journal of Biological Chemisty 288(16), 10967-10972 (2013).
4. Citric acid cycle intermediates as ligands for orphan G-
5. Expression and localization of GPR91 and GPR99 in murine organs. Cell Tissue Res. 364(2), 245-262 (2016).
6. Expression and localization of GPR99 in human nasal mucosa. Auris Nasus Larynx 44(2), 162-167 (2017).
7. Receptors of intermediates of carbohydrate metabolism, GPR91 and GPR99, mediate axon growth. PLoS Biol. 16(5), e2003619 (2018).