Product Description:

Name	TTR Full-Length MS Protein Standard
Cat#	CPFL304976
Protein Name	transthyretin
Symbol	TTR
Synonyms	CTS; CTS1; HEL111; HsT2651; PALB; TBPA
Accession	NM_000371
Cytogenetic	18q12.1
Amino Acid Labeled	[U- 13C6, 15N4]-L-Arg and [U- 13C6, 15N2]-L-Lys
Chemical Purity	> 80% as determined by SDS-PAGE and Coomassie blue staining
Expression Host	Human HEK293 cells
Predicted MW	13.7 kDa
Expression TrueORF Clone	RC204976
Description	TTR Full-Length MS Protein Standard (NP_000362), Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine, was produced in human 293 cells (HEK293) with fully chemically defined cell culture medium to obtain incorporation efficiency at Creative-Proteomics. This gene encodes transthyretin, one of the three prealbumins including alpha-1-antitrypsin, transthyretin and orosomucoid. Transthyretin is a carrier protein; it transports thyroid hormones in the plasma and cerebrospinal fluid, and also transports retinol (vitamin A) in the plasma. The protein consists of a tetramer of identical subunits. More than 80 different mutations in this gene have been reported; most mutations are related to amyloid deposition, affecting predominantly peripheral nerve and/or the heart, and a small portion of the gene mutations is non-amyloidogenic. The diseases caused by mutations include amyloidotic polyneuropathy, euthyroid hyperthyroxinaemia, amyloidotic vitreous opacities, cardiomyopathy, oculoleptomeningeal amyloidosis, meningocerebrovascular amyloidosis, carpal tunnel syndrome, etc.

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