RD3 (NM_183059) Human Mass Spec Standard

Specifications

Product Data
Description	RD3 MS Standard C13 and N15-labeled recombinant protein (NP_898882)
Species	Human
Expression Host	HEK293
Expression cDNA Clone or AA Sequence	RC209596
Predicted MW	22.7 kDa
Protein Sequence	Sequence Link (showhide) >RC209596 protein sequence Red=Cloning site Green=Tags(s) MSLISWLRWNEAPSRLSTRSPAEMVLETLMMELTGQMREAERQQRERSNAVRKVCTGVDYSWLASTPRST YDLSPIERLQLEDVCVKIHPSYCGPAILRFRQLLAEQEPEVQEVSQLFRSVLQEVLERMKQEEEAHKLTR QWSLRPRGSLATFKTRARISPFASDIRTISEDVERDTPPPLRSWSMPEFRAPKAD 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_898882
RefSeq Size	4290
RefSeq ORF	585
Synonyms	C1orf36; LCA12
Locus ID	343035
Cytogenetics	1q32.3
Summary	This gene encodes a retinal protein that is associated with promyelocytic leukemia-gene product (PML) bodies in the nucleus. Mutations in this gene cause Leber congenital amaurosis type 12, a disease that results in retinal degeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2009]

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