|Application ||WB, E|
|Other Accession||NP_005848, 10269|
|Calculated MW||54813 Da|
|Other Names||CAAX prenyl protease 1 homolog, 188.8.131.52, Farnesylated proteins-converting enzyme 1, FACE-1, Prenyl protein-specific endoprotease 1, Zinc metalloproteinase Ste24 homolog, ZMPSTE24, FACE1, STE24|
|Format||0.5 mg IgG/ml in Tris saline (20mM Tris pH7.3, 150mM NaCl), 0.02% sodium azide, with 0.5% bovine serum albumin|
|Storage||Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.|
|Precautions||Goat Anti-FACE1 / ZMPSTE24 Antibody is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||Proteolytically removes the C-terminal three residues of farnesylated proteins. Acts on lamin A/C.|
|Cellular Location||Endoplasmic reticulum membrane; Multi-pass membrane protein. Nucleus inner membrane; Multi-pass membrane protein|
|Tissue Location||Widely expressed. High levels in kidney, prostate, testis and ovary|
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Provided below are standard protocols that you may find useful for product applications.
This gene encodes a member of the peptidase M48A family. The encoded protein is a zinc metalloproteinase involved in the two step post-translational proteolytic cleavage of carboxy terminal residues of farnesylated prelamin A to form mature lamin A. Mutations in this gene have been associated with mandibuloacral dysplasia and restrictive dermopathy.
Variation at the NFATC2 Locus Increases the Risk of Thiazolinedinedione-Induced Edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) Study. Bailey SD, et al. Diabetes Care, 2010 Jul 13. PMID 20628086.
Novel frameshifting mutations of the ZMPSTE24 gene in two siblings affected with restrictive dermopathy and review of the mutations described in the literature. Smigiel R, et al. Am J Med Genet A, 2010 Feb. PMID 20101687.
Gene-centric association signals for lipids and apolipoproteins identified via the HumanCVD BeadChip. Talmud PJ, et al. Am J Hum Genet, 2009 Nov. PMID 19913121.
Polymorphisms of the lamina maturation pathway and their association with the metabolic syndrome: the DESIR prospective study. Fontaine-Bisson B, et al. J Mol Med, 2010 Feb. PMID 19841875.
Genetic variation in healthy oldest-old. Halaschek-Wiener J, et al. PLoS One, 2009 Aug 14. PMID 19680556.
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