ATOMIC MASS UNIT AND MOLECULAR WEIGHT

O-deacylate LPS [11]. The molecular mass of the majorsialylated glycoforms in the lgtC lic3A double mutant(3381.6 and 3546.0 Da) indicated the presence of anadditional 527 atomic mass units, corresponding to anN-acetyl-hexosamine residue and two hexose resid[r]

than heated MAPs, suggesting the loss during purification ofa cofactor required for maximal enzyme activity. No otherdescriptions of CoA esters and their hydrolysis products are,to our knowledge, available for Artemia.Secondary structure predictions for p49, 4-hydroxybuty-rate CoA-transferase[r]

they all assemble into a common complex or whetherthey are associated in different subcomplexes. To testthese possibilities, we subjected the TEV protease elu-ate obtained with Pex1p to 2D electrophoresis. Immu-noblot analysis identified Pex15p along with Pex1pand Pex6p in a complex of  880 kDa (Fig[r]

properties extremely slowly taking 3 days to achieve a which the average molecular weight is increasing withcompressive strength of 8 MPa, bulk density of 1.314, time. In the early stage, below the break point, the growingapparent porosity of 33.886 and Mohs hardness of 3–4. uni[r]

model 310 CE instrument (ATI Unicam, Boston, MA,USA) via a coaxial sheath–flow interface for sample injec-tion. A sheath solution (70 : 30, isopropanol–methanol)was delivered at a flow rate of 1.5 lLÆmin)1to a low deadvolume tee. Injections were performed on 90 cm length barefused silica at an applied[r]

and methods. Data represent mean values ± SD of three determinations from a representative experiment of 10.Ó FEBS 2003 Insulin signalling in rat hepatocytes (Eur. J. Biochem. 270) 4641In contrast, in liver preparations these novel insulinsignalling pathways have been poorly studied and