CABP4 (NM_145200) Human Mass Spec Standard

Specifications

Product Data
Description	CABP4 MS Standard C13 and N15-labeled recombinant protein (NP_660201)
Species	Human
Expression Host	HEK293
Expression cDNA Clone or AA Sequence	RC211536
Predicted MW	30.3 kDa
Protein Sequence	Sequence Link (showhide) >RC211536 representing NM_145200 Red=Cloning site Green=Tags(s) MTTEQARGQQGPNLAIGRQKPPAGVVTPKSDAEEPPLTRKRSKKERGLRGSRKRTGSSGEQTGPEAPGSS NNPPSTGEGPAGAPPASPGPASSRQSHRHRPDSLHDAAQRTYGPLLNRVFGKDRELGPEELDELQAAFEE FDTDRDGYISHRELGDCMRTLGYMPTEMELLEVSQHIKMRMGGRVDFEEFVELIGPKLREETAHMLGVRE LRIAFREFDRDRDGRITVAELREAVPALLGEPLAGPELDEMLREVDLNGDGTVDFDEFVMMLSRH 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_660201
RefSeq Size	1466
RefSeq ORF	825
Synonyms	CRSD; CSNB2B
Locus ID	57010
Cytogenetics	11q13.2
Summary	This gene encodes a member of the CABP family of calcium binding protein characterized by four EF-hand motifs. Mutations in this gene are associated with congenital stationary night blindness type 2B. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]

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