METTL27 (NM_152559) Human Mass Spec Standard

Specifications

Product Data
Description	WBSCR27 MS Standard C13 and N15-labeled recombinant protein (NP_689772)
Species	Human
Expression Host	HEK293
Expression cDNA Clone or AA Sequence	RC207050
Predicted MW	26.7 kDa
Protein Sequence	Sequence Link (showhide) >RC207050 protein sequence Red=Cloning site Green=Tags(s) MAQEEGGSLPEVRARVRAAHGIPDLAQKLHFYDRWAPDYDQDVATLLYRAPRLAVDCLTQALPGPPHSAL ILDVACGTGLVAAELRAPGFLQLHGVDGSPGMLEQARAPGLYQRLSLCTLGQEPLPSPEGTFDAVLIVGA LSDGQVPCNAIPELHVTKPGGLVCLTTRTNWSNLQYKEALEATLDRLEQAGMWEGLVAWPVDRLWTAGSW LPPSWWWYPASLPRMASSPALSTCTESGRRPRLRK 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_689772
RefSeq Size	958
RefSeq ORF	735
Synonyms	WBSCR27
Locus ID	155368
Cytogenetics	7q11.23
Summary	This gene encodes a protein belonging to ubiE/COQ5 methyltransferase family. The gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.22-q11.23. [provided by RefSeq, Jul 2008]

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