Table 1.

PCR primers for the amplification of ADAMTS13exons and adjacent intron sequences chosen from the published sequence (GenBank accession numbers AL158826 and AC002325)

ExonSenseAntisenseAT °C
ggg tcg acc cgg gtc gga aaa ctc gct ggc aga gag agg tgg cgc tgg cgg ccc agc ggg 68  
10 + 11 ggg act ctc tgt gtg tgt tgg g tga acc aca gat ggt cac ttt ggc tcc 62 
12 gtg cca tgt agt ctc cca gtg aca aca cc cca gag cct gaa cca ctt tgc cca gtg c 65  
15 caa ttt ttc ccg acc agc taa gat cag ctc act tgc ggg tga tgt cag aag tga ggg 64  
16 ctg tgg ctc ctt aga gga ggg ctg ggg cgc tga atg aat aaa tga acg aat cag gg 64 
20 gca gct ggg cta tac ctt ccc ctg gg aat ggg tgc tcc tcg ttc tcc cag cc 68  
21 gga tcg ctg ggt cct cag agg agg ccc gaa cga ggc aag atg caa gtg gac agg 65  
22 gag gtg tcc agt gag cct ggg ctg cag tcc ggc atg gag cca agg ctc agg tct cc 67 
26 cct cct ggt ctc ctt cct cag ctt gg tgc cag gaa tgg ggc atg cag cgt c 67  
27 ctt gaa ctc ggc tca gtc tac cct g ttc cat ctc agt cag ttc cct ccg 62  
28 acg gct ccc tgg ctg tga gtt gtc c ggg tcc cct agc cct gca cgc cc 68  
29 ccg tga gtg cta att att act tgt gg ggg ttt tca agc cag gtc tgg aca gc 61 
ExonSenseAntisenseAT °C
ggg tcg acc cgg gtc gga aaa ctc gct ggc aga gag agg tgg cgc tgg cgg ccc agc ggg 68  
10 + 11 ggg act ctc tgt gtg tgt tgg g tga acc aca gat ggt cac ttt ggc tcc 62 
12 gtg cca tgt agt ctc cca gtg aca aca cc cca gag cct gaa cca ctt tgc cca gtg c 65  
15 caa ttt ttc ccg acc agc taa gat cag ctc act tgc ggg tga tgt cag aag tga ggg 64  
16 ctg tgg ctc ctt aga gga ggg ctg ggg cgc tga atg aat aaa tga acg aat cag gg 64 
20 gca gct ggg cta tac ctt ccc ctg gg aat ggg tgc tcc tcg ttc tcc cag cc 68  
21 gga tcg ctg ggt cct cag agg agg ccc gaa cga ggc aag atg caa gtg gac agg 65  
22 gag gtg tcc agt gag cct ggg ctg cag tcc ggc atg gag cca agg ctc agg tct cc 67 
26 cct cct ggt ctc ctt cct cag ctt gg tgc cag gaa tgg ggc atg cag cgt c 67  
27 ctt gaa ctc ggc tca gtc tac cct g ttc cat ctc agt cag ttc cct ccg 62  
28 acg gct ccc tgg ctg tga gtt gtc c ggg tcc cct agc cct gca cgc cc 68  
29 ccg tga gtg cta att att act tgt gg ggg ttt tca agc cag gtc tgg aca gc 61 

Published primers were used for the remaining exons.18 Sense and antisense primers are both given in 5′-3′ direction. Screening for identified mutations among relatives of patients and 50 normal controls (100 alleles) was done either directly by polyacrylamide gel electrophoresis (PAGE) of PCR products in the case of a dinucleotide deletion, or by PAGE after restriction enzyme digest (Table 2). AT indicates annealing temperature.

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