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A new immunochemical method for the quantitative measurement of specific gene products in man-rodent somatic cell hybrids

โœ Scribed by P. G. Groot; M. N. Hamers; A. Westerveld; A. W. Schram; P. Meera Khan; J. M. Tager


Publisher
Springer
Year
1978
Tongue
English
Weight
514 KB
Volume
44
Category
Article
ISSN
0340-6717

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โœฆ Synopsis


An immunochemical method has been developed for the quantitative determination of species-specific gene products, for instance a-galactosidase and N-acetyl-a-galactosaminidase, in man-rodent hybrid cells and in the parental cell lines. Antisera raised against the purified enzymes are covalently coupled to Sepharose 4B. The gene products are specifically removed from a cell lysate by incubating with the appropriate Sepharose-coupled antiserum. After centrifugation followed by washing of the precipitated Sepharose, the enzymic activity can be quantitatively measured on the Sepharose beads. With this technique it has been demonstrated that the ability of human N-acetyl-agalactosaminidase (also known as a-galactosidase B) to hydrolyze a-galactosidfc linkages is lost when the enzyme is expressed in man-Chinese hamster hybrid cells.


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โœ Helen R. Palser; Phyllis J. McAlpine ๐Ÿ“‚ Article ๐Ÿ“… 1976 ๐Ÿ› Springer ๐ŸŒ English โš– 526 KB

Species-specific antibodies, prepared against unpurified human and Chinese hamster fibroblast extracts, were used to identify the parental origins of enzymes in human-hamster somatic cell hybrids. Results of the detection of the expression of the human glucosephosphate isomerase gene locus (GPI) by