AKT1 Validated Stealth™ DuoPack -"DISCONTINUED" - Citations

AKT1 Validated Stealth™ DuoPack -"DISCONTINUED" - Citations

View additional product information for AKT1 Validated Stealth™ DuoPack -"DISCONTINUED" - Citations (12935001)

Showing 4 product Citations

Citations & References
Abstract
Surface Calreticulin Mediates Muramyl Dipeptide-induced Apoptosis in RK13 Cells.
AuthorsChen D, Texada DE, Duggan C, Liang C, Reden TB, Kooragayala LM, Langford MP,
JournalJ Biol Chem
PubMed ID15817475
'Calreticulin (CRT) is a binding protein for apoptotic N-acetylmuramyl-l-alanyl-d-isoglutamine (l,d-MDP) or peptidoglycan in RK(13) cells. CRT on RK(13) cell surface (srCRT) forms complex(es) with tumor necrosis factor receptor 1 (TNFR1) and TNFR-associated death domain (TRADD) protein of the cell membrane. CRT polyclonal or monoclonal antibody binding to RK(13) srCRT dose-dependently ... More
Adenosine 2b receptor (A2bR) signals through adenylate cyclase (AC) 6 isoform in the intestinal epithelial cells.
AuthorsKolachala VL, Obertone TS, Wang L, Merlin D, Sitaraman SV,
JournalBiochim Biophys Acta
PubMed ID16631311
Adenosine 2b receptor (A2bR), a G-protein coupled receptor positively coupled to adenylate cyclase, mediates key events such as chloride, IL-6 and fibronectin secretion in intestinal epithelial cells and is upregulated during intestinal inflammation. In order to gain insight into the overall mechanism of A2bR activation, in this study, we sought ... More
Protein kinase C delta regulates Ser46 phosphorylation of p53 tumor suppressor in the apoptotic response to DNA damage.
AuthorsYoshida K, Liu H, Miki Y,
JournalJ Biol Chem
PubMed ID16377624
The p53 tumor suppressor is activated in the cellular response to genotoxic stress. Transactivation of p53 target genes dictates cell cycle arrest and DNA repair or induction of apoptosis; however, a molecular mechanism responsible for these distinct functions remains unclear. Recent studies revealed that phosphorylation of p53 on Ser(46) was ... More
Molecular cloning and characterization of a novel 3'-phosphoadenosine 5'-phosphosulfate transporter, PAPST2.
AuthorsKamiyama S, Sasaki N, Goda E, Ui-Tei K, Saigo K, Narimatsu H, Jigami Y, Kannagi R, Irimura T, Nishihara S,
JournalJ Biol Chem
PubMed ID16492677
Sulfation is an important posttranslational modification associated with a variety of molecules. It requires the involvement of the high energy form of the universal sulfate donor, 3'-phosphoadenosine 5'-phosphosulfate (PAPS). Recently, we identified a PAPS transporter gene in both humans and Drosophila. Although human colonic epithelial tissues express many sulfated glycoconjugates, ... More