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Complementary DNA for CD1b-TD was generated by polymerase chain reaction with the use of full-length CD1 b cDNA (1) as a template DNA. The primers used were 5′-AGCGGATCCAGTGAACATGCCTTCCAGGGG-3′ (plus strand, 5′ end of CD1b cDNA) and 5′-TCGGGATCCTAGCGCCTCATATACCATAA-3′ (minus strand, 3′ end). The amplified fragment was sequenced and subcloned into pSRα-neo for transfection into HeLa cells. The cytoplasmic amino acid sequences of CD1b-FL and CD1b-TD are Met-Arg-Arg-Arg-Ser-Tyr-Gln-Asn-Ile-Pro and Met-Arg-Arg, respectively.
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We thank H. Ploegh, J. Trowsdale, M. Fukuda, P. Cresswell, D. Olive, C. Mawas, V. Hsu, and W. Brown for their gifts of reagents; L. Glimcher of Harvard Medical School for the gift of expression vector p3-9; Genetics Institute (Cambridge, MA) for GMCSF; Schering-Plough Corp. (Kenilworth, NJ) for IL-4; and V. Hsu for critically reading the manuscript. Supported by grants from NIH.
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