IP R α Cyclin E. K-Ras V12. c-Myc. WT p27-/- CK- WT p27-/- CK- WT p27-/- CK-. M α P-HH1. IP R α CDK2. K-Ras V12. c-Myc. WT p27-/- CK- WT p27-/- CK- WT p27-/- CK-. 32 P-HH1. IP R α CDK1. K-Ras V12. c-Myc.
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Phospho Staining. The experiment mainly focuses on the staining of proteins which are phosphorylated during the post translational modification. Related LOs: Staining techniques.
siRNA-D5. ns-siRNA. untreated. p38MAPK. β-Actin. phospho-p38MAPK. β-Actin. b). 72 h. a).
Anti-Acetyl- and Phospho-Histone H3 polyclonal antibody
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Introduction. Calcium et phosphore =principaux constituants os (65% poids)Les os renferment ? totalit calcium et phosphore de l\'organismeRle crucial des quantits mineures de calcium et phosphore dans le sang dans de nombreux processus biologiquesImportance rgulation homostasie calcium phoph
LE METABOLISME PHOSPHO-CALCIQUE. Généralités Physiologie : Régulation du métabolisme phospho-calcique La Parathormone 1- Biosynthèse et métabolisme 2- Régulation 3- Actions physiologiques La Calcitonine La Vitamine D Exploration Dosages hormonaux, tests dynamiques Echographie
ECOLE NATIONALE VETERINAIRE T O U L O U S E. Le métabolisme Phospho-calcique. V. Gayrard Physiologie Ecole Nationale Vétérinaire De Toulouse 23, Chemin Des Capelles 31076 Toulouse. Introduction. Calcium (Ca 2+) et phosphate (Pi) =principaux constituants os (65% poids)
Raw blot for phospho-PI3K. Sample codes 13A=N1 27A=N2 OA 332=OA 1 OA 333=OA 2 OA 303=OA 3. OA 333. Ladder. 27A. OA 332. OA 303. OA 210. OA 247. 13A. OA 276. Raw blot for PI3K total. Using a film scanner (scanning using a light source). Using a regular document scanner. Ladder.