Human ACP6 Protein

<strong>Human ACP6 Protein</strong>_x000D_ <strong>Catalog number:</strong> B2011480_x000D_ <strong>Lot number:</strong> Batch Dependent_x000D_ <strong>Expiration Date:</strong> Batch dependent_x000D_ <strong>Amount:</strong> 100 µg_x000D_ <strong>Molecular Weight or Concentration:</strong> 1 mg/mL_x000D_ <strong>Supplied as:</strong> Solution_x000D_ <strong>Applications:</strong> molecular tool for various biochemical applications_x000D_ <strong>Storage:</strong> -20 °C_x000D_ <strong>Keywords:</strong> ACP6 protein (His tag), lysophosphatidic acid phosphatase type 6 protein, ACPL1 protein, LPAP protein, PACPL1 protein_x000D_ <strong>Grade:</strong> Biotechnology grade. All products are highly pure. All solutions are made with Type I ultrapure water (resistivity &gt;18 MΩ-cm) and are filtered through 0.22 um._x000D_ _x000D_ <strong>References:</strong>_x000D_ 1: Chryplewicz A, Tienda SM, Nahotko DA, Peters PN, Lengyel E, Eckert MA. Mutant p53 regulates LPA signaling through lysophosphatidic acid phosphatase type 6 Sci Rep. 2019 Mar 26;9(1):5195._x000D_ 2: Li J, Dong Y, Lü X, Wang L, Peng W, Zhang XC, Rao Z. Crystal structures and biochemical studies of human lysophosphatidic acid phosphatase type 6 Protein Cell. 2013 Jul;4(7):548-61._x000D_ 3: Calvo JH, Martínez-Royo A, Silveri L, Floriot S, Eggen A, Marcos-Carcavilla A, Serrano M. Isolation, mapping and identification of SNPs for four genes (ACP6, CGN, ANXA9, SLC27A3) from a bovine QTL region on BTA3 Cytogenet Genome Res. 2006;114(1):39-43._x000D_ 4: Pettersson M, Viljakainen H, Loid P, Mustila T, Pekkinen M, Armenio M, Andersson-Assarsson JC, Mäkitie O, Lindstrand A. Copy Number Variants Are Enriched in Individuals With Early-Onset Obesity and Highlight Novel Pathogenic Pathways J Clin Endocrinol Metab. 2017 Aug 1;102(8):3029-3039._x000D_ 5: Wolber LE, Steves CJ, Tsai PC, Deloukas P, Spector TD, Bell JT, Williams FM. Epigenome-wide DNA methylation in hearing ability: new mechanisms for an old problem PLoS One. 2014 Sep 3;9(9):e105729._x000D_ 6: Chen CP, Huang JP, Chen YY, Chern SR, Wu PS, Chen SW, Wang W, Lee CC. Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound Taiwan J Obstet Gynecol. 2019 Nov;58(6):859-863._x000D_ 7: Takayama I, Daigo Y, Ward SM, Sanders KM, Walker RL, Horowitz B, Yamanaka T, Fujino MA. Novel human and mouse genes encoding an acid phosphatase family member and its downregulation in W/W(V) mouse jejunum Gut. 2002 Jun;50(6):790-6._x000D_ 8: Christiansen J, Dyck JD, Elyas BG, Lilley M, Bamforth JS, Hicks M, Sprysak KA, Tomaszewski R, Haase SM, Vicen-Wyhony LM, Somerville MJ. Chromosome 1q21.1 contiguous gene deletion is associated with congenital heart disease Circ Res. 2004 Jun 11;94(11):1429-35._x000D_ 9: van der Meer JH, van der Poll T, van 't Veer C. TAM receptors, Gas6, and protein S: roles in inflammation and hemostasis Blood. 2014 Apr 17;123(16):2460-9._x000D_ <a href="https://pubmed.ncbi.nlm.nih.gov/9603986">10: Omura T. Mitochondria-targeting sequence, a multi-role sorting sequence recognized at all steps of protein import into mitochondria J Biochem. 1998 Jun;123(6):1010-6. </a>_x000D_ _x000D_ <strong>Products Related to Human ACP6 Protein can be found at</strong> <a href="https://moleculardepot.com/product-category/Proteins/"> Proteins</a>