FOXI1 (NM_144769) Human Mass Spec Standard

Specifications

Product Data
Description	FOXI1 MS Standard C13 and N15-labeled recombinant protein (NP_658982)
Species	Human
Expression Host	HEK293
Expression cDNA Clone or AA Sequence	RC206430
Predicted MW	30.8 kDa
Protein Sequence	Sequence Link (showhide) >RC206430 protein sequence Red=Cloning site Green=Tags(s) MSSFDLPAPSPPRCSPQFPSIGQEPPEMNLYYENFFHPQGVPSPQRPSFEGGGEYGATPNPYLWFNGPTM TPPPYLPGPNASPFLPQAYGVQRPLLPSVSGLGGSDLGWLPIPSQEELMKLVRPPYSYSALIAMAIHGAP DKRLTLSQIYQYVADNFPFYNKSKAGWQNSIRHNLSLNDCFKKVPRDEDDPAYVSGGSPTSHPLVTPGLS PEPSDKTGQNSLTFNSFSPLTNLSNHSGGGDWANPMPTNMLSYGGSVLSQFSPHFYNSVNTSGVLYPREG TEV 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_658982
RefSeq Size	2011
RefSeq ORF	849
Synonyms	FKH10; FKHL10; FREAC-6; FREAC6; HFH-3; HFH3
Locus ID	2299
Cytogenetics	5q35.1
Summary	This gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. This gene may play an important role in the development of the cochlea and vestibulum, as well as in embryogenesis. The encoded protein has been found to be required for the transcription of four subunits of a proton pump found in the inner ear, the kidney, and the epididymis. Mutations in this gene have been associated with deafness, autosomal recessive 4. [provided by RefSeq, Jan 2017]
Protein Families	Transcription Factors

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