DGCR6L (NM_033257) Human Mass Spec Standard

Specifications

Product Data
Description	DGCR6L MS Standard C13 and N15-labeled recombinant protein (NP_150282)
Species	Human
Expression Host	HEK293
Expression cDNA Clone or AA Sequence	RC200317
Predicted MW	24.9 kDa
Protein Sequence	Sequence Link (showhide) >RC200317 protein sequence Red=Cloning site Green=Tags(s) MERYAAALEEVADGARQQERHYQLLSALQSLVKELPSSFQQRLSYTTLSDLALALLDGTVFEIVQGLLEI QHLTEKSLYNQRLRLQNEHRVLRQALRQKHQEAQQACRPHNLPVVQAAQQRELEAVEHRIREEQRAMDQK IILELDRKVADQQSTLEKAGVAGFYVTTNPQELMLQMNLLELIRKLQQRGCRAGNAALGLGGPWQSPAAQ CDQKGSPVPP 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_150282
RefSeq Size	1217
RefSeq ORF	660
Synonyms	DGCR6
Locus ID	85359
Cytogenetics	22q11.21
Summary	This gene, the result of a duplication at this locus, is one of two functional genes encoding nearly identical proteins that have similar expression patterns. The product of this gene is a protein that shares homology with the Drosophila gonadal protein, expressed in gonadal tissues and germ cells, and with the human laminin gamma-1 chain that functions in cell attachment and migration. This gene is located in a region of chromosome 22 implicated in the DiGeorge syndrome, one facet of a broader collection of anomalies referred to as the CATCH 22 syndrome. [provided by RefSeq, Jul 2008]
Protein Families	Druggable Genome, Transcription Factors

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