Abstract
The DR beta/SstI system identified the 28 fragments as shown in Figure 1 and Table 1. Some close fragments from St. fragment no. 8 to no. 14 were difficult to analyze even in the long migration condition. St. fragment no. 4, no. 22, and no. 25 were found only in a single laboratory. Two fragments (no. 22 and no. 25) are DQ-dominant. Cross-hybridizing bands are shown in Table 2. Of the 28 fragments, 18 are dominantly DR-specific. St. fragment no. 16 and no. 17 are DR-DO codominant. Six fragments are DQ-dominant and four are DP- dominant. Fine bands (St. fragment no. 1, no. 6, no. 7, no. 14, and no. 28) showed no cross-hybridization with other beta probes. The fragments absence/presence data on each cell line with the DRĪ² probe are shown in Table 3. St. fragment no. 12 (11.59 kb) and no. 16 (6.15kb) are highly correlated with DR1 and DRw15, respectively. St. fragment no. 2 (21.12kb), no. 14 (10.95kb), and no. 17 (5.19kb) are shown the common banding pattern in each of the 72 core cell lines. Twenty-two cell lines showed these three bands, including all but one of the DRw53 cells.
Participating Laboratories: JAPTSU,1 JAPSAS,2 BENREE3
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Ā© 1989 Springer-Verlag New York
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Ando, A., Sasazuki, T., Reekers, P., Tsuji, K. (1989). RFLP Standardization Report for DR Beta/SstI. In: Dupont, B. (eds) Immunobiology of HLA. Springer, New York, NY. https://doi.org/10.1007/978-1-4612-3552-1_119
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DOI: https://doi.org/10.1007/978-1-4612-3552-1_119
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