This webpage contains legacy information. The product is either no longer available from the supplier or has been delisted at Labome.
product summary
company name :
MilliporeSigma
other brands :
FLUKA, Sigma-Aldrich, Roche Applied Science
product type :
protein
product name :
Prealbumin from human plasma
catalog :
P1742
citations: 33
Reference
Tsuchiya Y, Byrne D, Burgess S, Bormann J, Bakovic J, Huang Y, et al. Covalent Aurora A regulation by the metabolic integrator coenzyme A. Redox Biol. 2020;28:101318 pubmed publisher
Niemietz C, Fleischhauer L, Sandfort V, Guttmann S, Zibert A, Schmidt H. Hepatocyte-like cells reveal novel role of SERPINA1 in transthyretin amyloidosis. J Cell Sci. 2018;131: pubmed publisher
Miller M, Pal A, Albusairi W, Joo H, Pappas B, Haque Tuhin M, et al. Enthalpy-Driven Stabilization of Transthyretin by AG10 Mimics a Naturally Occurring Genetic Variant That Protects from Transthyretin Amyloidosis. J Med Chem. 2018;61:7862-7876 pubmed publisher
Lourenço P, Silva S, Friões F, Alvelos M, Amorim M, Couto M, et al. Low prealbumin is strongly associated with adverse outcome in heart failure. Heart. 2014;100:1780-5 pubmed publisher
Lozeron P, Lacroix C, Théaudin M, Richer A, Gugenheim M, Adams D, et al. An amyotrophic lateral sclerosis-like syndrome revealing an amyloid polyneuropathy associated with a novel transthyretin mutation. Amyloid. 2013;20:188-92 pubmed publisher
Petrakis I, Mavroeidi V, Stylianou K, Andronikidi E, Lioudaki E, Perakis K, et al. Hsf-1 affects podocyte markers NPHS1, NPHS2 and WT1 in a transgenic mouse model of TTRVal30Met-related amyloidosis. Amyloid. 2013;20:164-72 pubmed publisher
Beirão J, Matos M, Beirão I, Costa P, Torres P. Topical cyclosporine for severe dry eye disease in liver-transplanted Portuguese patients with familial amyloidotic polyneuropathy (ATTRV30M). Eur J Ophthalmol. 2013;23:156-63 pubmed publisher
Adams D, Samuel D, Slama M. [Treatment of familial amyloid polyneuropathy]. Presse Med. 2012;41:793-806 pubmed publisher
Kodaira M, Morita H, Shimojima Y, Ikeda S. Electrophysiological features of familial amyloid polyneuropathy in endemic area. Amyloid. 2011;18:10-8 pubmed publisher
Trivella D, Bleicher L, Palmieri L, Wiggers H, Montanari C, Kelly J, et al. Conformational differences between the wild type and V30M mutant transthyretin modulate its binding to genistein: implications to tetramer stability and ligand-binding. J Struct Biol. 2010;170:522-31 pubmed publisher
Dardiotis E, Koutsou P, Zamba Papanicolaou E, Vonta I, Hadjivassiliou M, Hadjigeorgiou G, et al. Complement C1Q polymorphisms modulate onset in familial amyloidotic polyneuropathy TTR Val30Met. J Neurol Sci. 2009;284:158-62 pubmed publisher
Said G, Plante Bordeneuve V. Familial amyloid polyneuropathy: a clinico-pathologic study. J Neurol Sci. 2009;284:149-54 pubmed publisher
Munar Ques M, Martinez Nadal J, Torres Rovira J, Sole M, Zabay Becerril J, Mulet Ferrer J. Finding of vascular amyloid TTR in inferior nasal concha in a patient with FAP TTRVal30Met. Amyloid. 2008;15:272-4 pubmed publisher
Koike H, Kawagashira Y, Iijima M, Yamamoto M, Hattori N, Tanaka F, et al. Electrophysiological features of late-onset transthyretin Met30 familial amyloid polyneuropathy unrelated to endemic foci. J Neurol. 2008;255:1526-33 pubmed publisher
Rudolph T, Kurz M, Farbu E. Late-onset familial amyloid polyneuropathy (FAP) Val30Met without family history. Clin Med Res. 2008;6:80-2 pubmed publisher
Liu L, Liu J, Dai S, Wang X, Wu S, Wang J, et al. Reduced transthyretin expression in sera of lung cancer. Cancer Sci. 2007;98:1617-24 pubmed
Ito T, Sakakibara R, Ito S, Uchiyama T, Liu Z, Yamamoto T, et al. Mechanism of constipation in familial amyloid polyneuropathy: a case report. Intern Med. 2006;45:1173-5 pubmed
Sobue G. [Clinical phenotype of Charcot-Marie-Tooth disease (CMT) and familial amyloid polyneuropathy (FAP)]. Rinsho Shinkeigaku. 2003;43:769-74 pubmed
Ohmori H, Ando Y, Makita Y, Onouchi Y, Nakajima T, Saraiva M, et al. Common origin of the Val30Met mutation responsible for the amyloidogenic transthyretin type of familial amyloidotic polyneuropathy. J Med Genet. 2004;41:e51 pubmed
Koga T, Ando E, Hirata A, Fukushima M, Kimura A, Ando Y, et al. Vitreous opacities and outcome of vitreous surgery in patients with familial amyloidotic polyneuropathy. Am J Ophthalmol. 2003;135:188-93 pubmed
Harada T, Ishizaki F, Togo M, Yamashita H, Nitta K, Date Y, et al. [A sporadic case of late-onset familial amyloid polyneuropathy type I (transthyretin Met 30-associated familial amyloid polyneuropathy) inborn habitant of Ehime prefecture]. No To Shinkei. 2002;54:615-9 pubmed
Figueras J, Munar Ques M, Pares D, Torras J, Fabregat J, Rafecas A, et al. [Sequential liver transplantation: description of the first three patients in Spain]. Med Clin (Barc). 2001;116:377-9 pubmed
Herlenius G, Larsson M, Ericzon B. FAP World Transplant Register and domino/sequential register update. Transplant Proc. 2001;33:1367 pubmed
Tashima K, Ando Y, Terazaki H, Yoshimatsu S, Suhr O, Obayashi K, et al. Outcome of liver transplantation for transthyretin amyloidosis: follow-up of Japanese familial amyloidotic polyneuropathy patients. J Neurol Sci. 1999;171:19-23 pubmed
Misu K, Hattori N, Nagamatsu M, Ikeda S, Ando Y, Nakazato M, et al. Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan. Clinicopathological and genetic features. Brain. 1999;122 ( Pt 10):1951-62 pubmed
Monteiro E, Perdigoto R, Furtado A. Liver transplantation for familial amyloid polyneuropathy. Hepatogastroenterology. 1998;45:1375-80 pubmed
Inouye H, Domingues F, Damas A, Saraiva M, Lundgren E, Sandgren O, et al. Analysis of x-ray diffraction patterns from amyloid of biopsied vitreous humor and kidney of transthyretin (TTR) Met30 familial amyloidotic polyneuropathy (FAP) patients: axially arrayed TTR monomers constitute the protofilament. Amyloid. 1998;5:163-74 pubmed
Suess K, Moch H, Epper R, Koller A, Dürmüller U, Mihatsch M. [Heterogeneity of seminal vesicle amyloid. Immunohistochemical detection of lactoferrin and amyloid of the prealbumin-transthyretin type]. Pathologe. 1998;19:115-9 pubmed
Saraiva M, Almeida M, Alves I, Bonifacio M, Damas A, Palha J, et al. Modulating conformational factors in transthyretin amyloid. Ciba Found Symp. 1996;199:47-52; discussion 52-7 pubmed
Shimizu H, Ishikawa K, Kobayashi H, Murakami T, Nakazato M, Miura K, et al. [Familial amyloidotic polyneuropathy with a transthyretin variant (Val30-->Leu)]. No To Shinkei. 1996;48:175-8 pubmed
Hanes D, Zech L, Murrell J, Benson M. Metabolism of normal and Met30 transthyretin. Adv Food Nutr Res. 1996;40:149-55 pubmed
Ciulla T, Tolentino F, Morrow J, Dryja T. Vitreous amyloidosis in familial amyloidotic polyneuropathy. Report of a case with the Val30Met transthyretin mutation. Surv Ophthalmol. 1995;40:197-206 pubmed
Nelson K, Pollack S, Hellstrom K. Specific anti-tumor responses by cultured immune spleen cells. I. In vitro culture method and initial characterization of factors which block immune cell-mediated cytotoxicity in vitro. Int J Cancer. 1975;15:806-14 pubmed
product information
Catalog Number :
P1742
Product Name :
Prealbumin from human plasma
Product Type :
PROTEINS & ENZYMES
Product Group :
Protein & Pathway Technologies
Product Description :
lyophilized powder
company information
MilliporeSigma
PO Box 14508
St. Louis, MO 63178
https://www.sigmaaldrich.com
1-800-325-3010
headquarters: USA