Porcine aorta

Bovine aorta smooth muscle cells Bovine aorta endothelial cells Porcine aorta endothelial cells Rat keratinocytes... 

Sandberg, L. B., Weissman, N., and Smith, D. W. The purification and partial characterization of a soluble elastin-like protein from copper-deficient porcine aorta. Biochemistry 8, 2940-2945 (1969). 

Fig. 3.10 Porcine aorta sections bonded with adhesive cured with polymerization (red arrow shows adhesive bond (see Fig. 3.13).

Fig. 3.15 Tensile test of end to end bonded porcine aorta at break...

A Banyu patent, which describes 203 compounds, highlights a very similar compound (example 50) (28) which is reported to show 87% inhibition at 1.1 //M of ET-1 binding in porcine aorta receptors, and activity in vitro in the guinea-pig trachea and on rat heart perfusion pressure. There is no other published information on this series of compounds. 

Friedl P, Chang JJ Tatje D (1989) Different oxygen sensitivities of vascular endothelial cells from porcine aorta and from human veins during fermentation in a stirred bioreactor. In Spier RE, Griffiths JB, Stephenne J Crooy PJ (eds) Advances in Animal Cell Biology and Technology for Bioprocesses, pp. 233-237. Butterworth, London. 

Stegeman, J., M. Hahn, R. Weisbrod, B. Woodin, J. Joy, S. Najibi and R. Cohen. Induction of cytochrome P4501A1 by aryl hydrocarbon receptor agonists in porcine aorta endothelial cells in culture and cytochrome P4501A1 activity in intact cells. Mol. Pharmacol. 47 296-306, 1995. 

Watanabe et al. (1992) sequenced chemically the LC20 of porcine aorta myosin. There was only one amino acid substitution compared with chicken gizzard and two substitutions compared with human umbilical artery smooth muscle LC20. It is noteworthy that the substitutions never take place at positions 18 and 19, the phosphorylation sites for MLCK, or at positions 1, 2, and 9, the phosphorylation sites for PKC. 

Hasegawa et al. (1992) sequenced LClTa and LClTb of porcine aorta myosin (Fig. 9), both containing 150 amino acid residues with acetylated N-terminal cysteines. Only the C-terminal region differs between the... 

The physiological role of LC17 isoforms has been studied by several investigators. The actin-activated MgATPase activity of phosphorylated and non-phosphorylated myosin from porcine gastric corpus (0% LClTb, Table I) was twofold higher that that of myosin from porcine aorta (43% LClTb) (Helper et al.,... 

Recently, the cofactor peptides have also been isolated from semicarbazide-sensitive amine oxidases purified from bovine and porcine aortas [52], sequenced and confirmed to contain the topa quinone. The same topa quinone consensus sequence was also found in the primary structures of amine oxidases from human kidney [53], human retina [54] and rat colon [55], so called amiloride-binding proteins , and amine oxidase from human placenta [56] that shows 81% identity with bovine plasma amine oxidase [57], bovine lung amine oxidase [58], and amine oxidases from pea and lentil seedlings [59,60], chick pea seedlings [61], and Arabidopsis thaliana [62] obtained by the molecular cloning of respective DNAs. 

Porcine aorta (semicarbazide sensitive amine oxidase) NxDYY [52]... 

Application -Cardiovascular application (Hemocompat-ibility] [88] -Cardiovascular application (similarity of mechanical properties to those of porcine aorta and aortic heart valve] [89]... 

Chambers, Forsee and Elbein (1977) and Forsee, Griffin and Schutzback (1977) studied the further addition of mannosyl residues to large mannosyl glycolipids using microsomes from rabbit liver and porcine aorta. 

Figure 12. Photograph of endothelial cells (porcine aorta) grown directly on a porphyrinic sensor (deposited on recticulated vitrous carbon (RVC)).

---