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OriGene & ISB Alliance to Create a SRM/MRM Standard Database for 5,000 Human Proteins

Rockville, MD/Seattle, WA ?May 11, 2010 ?OriGene and the Institute for Systems Biology (ISB), announce plans to create a proteotypic PeptideAtlas and develop an SRM/MRM mass spectrometry standard database for 5,000 human proteins (Press Release)

Dr. Leroy Hood on Proteome Project at OriGene's ASMS2010 Luncheon Dr. Leroy Hood Presentation on ASMS 2010

Dr. Wei-wu He on Development of Assays for Every Human Protein Dr. Weiwu He Presentation on ASMS 2010

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JUP Mass Spec Standard

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Specifications Related Products FAQs
Cat. No. Ref. ID Description Price Shipping
PH304209 NM_002230 JUP MS Standard C13 and N15-labeled recombinant protein (NP_002221), 10 ug $ 1500 3 weeks

Also for JUP (NM_002230)

OriGene Data
Expression Host:Human HEK293 cells Predicted MW:81.6 kDa
Expression TrueORF clone:RC204209 Protein Sequence: Sequence Link
Tag:C-terminal MYC/DDK * Anti-Myc/DDK antibody Protein family:
Purity:> 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration:> 50 ug/ml as determined by BCA
Labeling Method:Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine
Labeling Efficiency:> 90% incorporation
Buffer and Storage:100 mM glycine, 25 mM Tris-HCl, pH 7.3. Store at -80C. Avoid repeated freeze-thaw cycles. Stable for 3 months from receipt of products under proper storage and handling conditions.
Protein Image
*: DDK-tag is the same as FLAG tag. Flag® is a registered trademark of Sigma-Aldrich

Reference Data
RefSeq: NP_002221 RefSeq Size: 3490 RefSeq ORF: 2238
Synonyms : ARVD12; CTNNG; DP3; DPIII; PDGB; PKGB
LocusID: 3728 Cytogenetic: 17q21  
Summary: This gene encodes a major cytoplasmic protein which is the only known constituent common to submembranous plaques of both desmosomes and intermediate junctions. This protein forms distinct complexes with cadherins and desmosomal cadherins and is a member of the catenin family since it contains a distinct repeating amino acid motif called the armadillo repeat. Mutation in this gene has been associated with Naxos disease. Alternative splicing occurs in this gene; however, not all transcripts have been fully described. [provided by RefSeq, Jul 2008].

 

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