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Abstract
An efficient method is described for the isolation of mouse hair follicle mRNAs. The
RNA contains two peaks of mRNA activity, 11s and 18s. The larger-sized group of mRNAs
encodes keratins of 46K, 47K, 58K, 59K, and 63K Mr. cDNAs were prepared using the
follicular mRNAs as templates and cloned to produce a library. Initial screening of
this library has identified five acidic and six basic mouse hair keratin clones.
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References
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Article info
Footnotes
☆Supported in part by NIH Grants 1 F32 AMO6577-01, AM21358, 1 R23 AM35644-01, a grant from Estee Lauder, Inc., and a grant from the Rudolf L. Baer Foundation for Skin Diseases, Inc.
Identification
Copyright
© 1988 Published by Elsevier Inc.
