IFITM5 (NM_001025295) Human Mass Spec Standard

Specifications

Product Data
Description	IFITM5 MS Standard C13 and N15-labeled recombinant protein (NP_001020466)
Species	Human
Expression Host	HEK293
Expression cDNA Clone or AA Sequence	RC213834
Predicted MW	14.2 kDa
Protein Sequence	Sequence Link (showhide) >RC213834 representing NM_001025295 Red=Cloning site Green=Tags(s) MDTAYPREDTRAPTPSKAGAHTALTLGAPHPPPRDHLIWSVFSTLYLNLCCLGFLALAYSIKARDQKVVG DLEAARRFGSKAKCYNILAAMWTLVPPLLLLGLVVTGALHLARLAKDSAAFFSTKFDDADYD 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_001020466
RefSeq Size	733
RefSeq ORF	396
Synonyms	BRIL; DSPA1; fragilis4; Hrmp1; OI5
Locus ID	387733
Cytogenetics	11p15.5
Summary	This gene encodes a membrane protein thought to play a role in bone mineralization. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195). [provided by RefSeq, Aug 2012]
Protein Families	Transmembrane

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