TM4SF20 (NM_024795) Human Mass Spec Standard

Specifications

Product Data
Description	TM4SF20 MS Standard C13 and N15-labeled recombinant protein (NP_079071)
Species	Human
Expression Host	HEK293
Expression cDNA Clone or AA Sequence	RC207725
Predicted MW	25.1 kDa
Protein Sequence	Sequence Link (showhide) >RC207725 protein sequence Red=Cloning site Green=Tags(s) MTCCEGWTSCNGFSLLVLLLLGVVLNVIPLIVSLVEEDQFSQNPISCFEWWFPGIIGAGLMAIPATTMSL TARKRACCNNRTGMFLSSFFSVITVIGALYCMLISIQALLKGPLMCNSPSNSNANCEFSLKNISDIHPES FNLQWFFNDSCAPPTGFNKPTSNDTMASGWRASSFHFDSEENKHRLIHFSVFLGLLLVGILEVLFGLSQI VIGFLGCLCGVSKRRSQIV 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_079071
RefSeq Size	2310
RefSeq ORF	687
Synonyms	PRO994; SLI5; TCCE518
Locus ID	79853
Cytogenetics	2q36.3
Summary	The protein encoded by this gene is a member of the four-transmembrane L6 superfamily. Members of this family function in various cellular processes including cell proliferation, motility, and adhesion via their interactions with integrins. In human brain tissue, this gene is expressed at high levels in the parietal lobe, occipital lobe, hippocampus, pons, white matter, corpus callosum, and cerebellum. Knockout of the homologous gene in mouse results in a neurobehavioral phenotype with suggested enhanced motor coordination. A deletion mutation in the human gene is associated with specific language impairment-5. [provided by RefSeq, Jul 2016]
Protein Families	Transmembrane

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