From this fact its crosslinked and high molecular weight nature has been deduced.
This is because higher molecular weight molecules are less soluble in water.
With post-anthesis shade, there was an increase in the proportion of lower molecular weight proteins (12 % origin) when compared with no shade conditions.
Pre-anthesis shading decreased yield and produced an increase in the protein fractions of higher molecular weight.
Polymeric proteins of higher molecular weight (4 and 6 % origins) increased when shading was provided prior to anthesis.
Due to their low molecular weight, they pass into the placenta and the fetus easily.
This suggests that the molecular sieve for the low molecular weight dextrans is distributed throughout the surface matrix layer.
Awareness about the importance of prophylaxis is relatively widespread, particularly in reference to low molecular weight heparin.
