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Quantitative fUm detection of ~ and 14C in polyacrylamide gels by fluorography. Eur I Biochem, 56, 335-341,1975 Orwin OF. Acid phosphatase distribution in the wool follicle. I U1trastruct Res, 55, 312-342,1976 Jones LN, Fowler KJ, Marshall RC, Ackland ML. Studies of developing human hair shaft cells in vitro. I Invest Dennatol, 90, 58-64, 1988 Heid HW, Werner E, Franke WW. The complement of native a-keratin polypeptides of hair forming cells: a subset of eight polypeptides that differ from epithelial cytokeratins.
The first one is that LSP are synthesized in the bulb, and did not seem to be modified in the keratogenous zone and in the fiber. 13 who found that cultured 'presumptive hair shaft' showed a continuing synthesis of LSP. The modification of the electrophoretic mobility due to the SCM, which provided different MW, the analysis of bulb SCM proteins in SDS-PAGE and the results given by Heid et al. 14 were similar. The second point is that aggregates, corresponding to unresolved proteins with very high MW, were not detectable in the bulb but appeared in the keratogenous zone and in hair fiber (Figure 3).
Anal Biochem, 72, 248-254,1976 Laemmli UK. Cleavage of structural proteins during the assembly of the head ofbacteriophage T4. Nature, 227, 680-685, 1970 Davis BJ. Disc electrophoresis. II: Method and application to human serum proteins. Ann NYAcad Sci, 121, 404-427, 1964 Laskey RA, Mills AD. Quantitative fUm detection of ~ and 14C in polyacrylamide gels by fluorography. Eur I Biochem, 56, 335-341,1975 Orwin OF. Acid phosphatase distribution in the wool follicle. I U1trastruct Res, 55, 312-342,1976 Jones LN, Fowler KJ, Marshall RC, Ackland ML.
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