ViraPower™ HiPerform™ T-REx™ Gateway™ Vector Kit - Citations

ViraPower™ HiPerform™ T-REx™ Gateway™ Vector Kit - Citations

View additional product information for ViraPower™ HiPerform™ T-REx™ Gateway™ Vector Kit - Citations (A11144)

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Citations & References
Abstract
Endothelial cell surface F1-F0 ATP synthase is active in ATP synthesis and is inhibited by angiostatin.
AuthorsMoser TL, Kenan DJ, Ashley TA, Roy JA, Goodman MD, Misra UK, Cheek DJ, Pizzo SV
JournalProc Natl Acad Sci U S A
PubMed ID11381144
'Angiostatin blocks tumor angiogenesis in vivo, almost certainly through its demonstrated ability to block endothelial cell migration and proliferation. Although the mechanism of angiostatin action remains unknown, identification of F(1)-F(O) ATP synthase as the major angiostatin-binding site on the endothelial cell surface suggests that ATP metabolism may play a role ... More
Characterization of peroxisomal Pex5p from rat liver. Pex5p in the Pex5p-Pex14p membrane complex is a transmembrane protein.
AuthorsGouveia AM, Reguenga C, Oliveira ME, Sa-Miranda C, Azevedo JE
JournalJ Biol Chem
PubMed ID10889202
Pex5p is the receptor for the vast majority of peroxisomal matrix proteins. Here, we show that about 15% of rat liver Pex5p is found in the peroxisomal fraction representing 0.06% of total peroxisomal protein. This population of Pex5p displays all the characteristics of an intrinsic membrane protein. Protease protection assays ... More