PCYT1A (NM_005017) Human Mass Spec Standard

Specifications

Product Data
Description	PCYT1A MS Standard C13 and N15-labeled recombinant protein (NP_005008)
Species	Human
Expression Host	HEK293
Expression cDNA Clone or AA Sequence	RC208130
Predicted MW	41.6 kDa
Protein Sequence	Sequence Link (showhide) >RC208130 representing NM_005017 Red=Cloning site Green=Tags(s) MDAQCSAKVNARKRRKEAPGPNGATEEDGVPSKVQRCAVGLRQPAPFSDEIEVDFSKPYVRVTMEEASRG TPCERPVRVYADGIFDLFHSGHARALMQAKNLFPNTYLIVGVCSDELTHNFKGFTVMNENERYDAVQHCR YVDEVVRNAPWTLTPEFLAEHRIDFVAHDDIPYSSAGSDDVYKHIKEAGMFAPTQRTEGISTSDIITRIV RDYDVYARRNLQRGYTAKELNVSFINEKKYHLQERVDKVKKKVKDVEEKSKEFVQKVEEKSIDLIQKWEE KSREFIGSFLEMFGPEGALKHMLKEGKGRMLQAISPKQSPSSSPTRERSPSPSFRWPFSGKTSPPCSPAN LSRHKAAAYDISEDEED TRTRPLEQKLISEEDLAANDILDYKDDDDKV
Tag	C-Myc/DDK
Purity	> 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration	>0.05 µg/µL as determined by microplate BCA method
Labeling Method	Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine
Buffer	25 mM Tris-HCl, 100 mM glycine, pH 7.3
Reference Data
RefSeq	NP_005008
RefSeq Size	1677
RefSeq ORF	1101
Synonyms	CCTA; CCTalpha; CT; CTA; CTPCT; PCYT1; SMDCRD
Locus ID	5130
Cytogenetics	3q29
Summary	This gene belongs to the cytidylyltransferase family and is involved in the regulation of phosphatidylcholine biosynthesis. Mutations in this gene are associated with spondylometaphyseal dysplasia with cone-rod dystrophy. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Aug 2015]
Protein Pathways	Glycerophospholipid metabolism, Metabolic pathways

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