FOXL2 (NM_023067) Human Mass Spec Standard

Specifications

Product Data
Description	FOXL2 MS Standard C13 and N15-labeled recombinant protein (NP_075555)
Species	Human
Expression Host	HEK293
Expression cDNA Clone or AA Sequence	RC209127
Predicted MW	38.6 kDa
Protein Sequence	Sequence Link (showhide) >RC209127 representing NM_023067 Red=Cloning site Green=Tags(s) MMASYPEPEDAAGALLAPETGRTVKEPEGPPPSPGKGGGGGGGTAPEKPDPAQKPPYSYVALIAMAIRES AEKRLTLSGIYQYIIAKFPFYEKNKKGWQNSIRHNLSLNECFIKVPREGGGERKGNYWTLDPACEDMFEK GNYRRRRRMKRPFRPPPAHFQPGKGLFGAGGAAGGCGVAGAGADGYGYLAPPKYLQSGFLNNSWPLPQPP SPMPYASCQMAAAAAAAAAAAAAAGPGSPGAAAVVKGLAGPAASYGPYTRVQSMALPPGVVNSYNGLGGP PAAPPPPPHPHPHPHAHHLHAAAAPPPAPPHHGAAAPPPGQLSPASPATAAPPAPAPTSAPGLQFACARQ PELAMMHCSYWDHDSKTGALHSRLDL SGPTRTRRLEQKLISEEDLAANDILDYKDDDDKV
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_075555
RefSeq Size	2744
RefSeq ORF	1128
Synonyms	BPES; BPES1; PFRK; PINTO; POF3
Locus ID	668
Cytogenetics	3q22.3
Summary	This gene encodes a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and may play a role in ovarian development and function. Expansion of a polyalanine repeat region and other mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3. [provided by RefSeq, Jul 2016]
Protein Families	Druggable Genome, Transcription Factors

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