Animal Selected For Lacking Heparan Sulfate-3-O-Sulfotransferase-1 and Uses Thereof
a technology of heparan sulfate and sulfate, which is applied in the field of animals selected for lacking heparan sulfate-3-o-sulfotransferase-1 and uses thereof, can solve the problems of unclear whether hssup> is hs, the level of at activity is not clear, and the patient is predisposed to venous thrombosis
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Generation of Hs3st1 − / − Mice
[0071] The Hs3st1 coding region was isolated by PCR screening an arrayed P1 library of 129P2 / OlaHsd genomic DNA (Incyte Genomics, St. Louis, Mo.) with two different oligonucleotide sets designed to amplify 5′ and 3′ untranslated region sequences of Hs3st1. Primers 5′-dATTGGCAACTGGAGATACTCATGT (SEQ ID NO:1) and 5′-dTGCCTTCTCCGGTGTCCTCT (SEQ ID NO:2) amplify nucleotides 219-467; whereas, 5′-dTTCTGTACAGTATTAGATTCACAGT (SEQ ID NO:3) with 5′-dGCTATTTTGGATTGGAGGCAGGT (SEQ ID NO: 4) amplify nucleotides 1383-1617 from the mouse Hs3st1 cDNA sequence (Shworak, et al. (1997) supra). Three independent overlapping genomic clones were recovered, exons were mapped by Southern blot analysis and the coding region was verified by DNA sequence analysis to reveal that exon 8 contained the entire coding region.
[0072] A targeting construct was generated from pMCIDT-A which contains an expression cassette for diphtheria toxin A (DTA) for positive selection. The targeting con...
example 2
Characterization of 3-OST-1 Deficient Mice
[0076] All experimental animals were generated from Hs3st1+ / −×Hs3st1+ / − crosses. Experimental groupings employed age and sex matched littermates. Unless otherwise indicated, all data are expressed as the mean±S.E.M. and statistical significance was evaluated by two-tailed Student's t-test.
[0077] For analysis of T·AT complexes, immediately after arterial injury a 0.5 cc syringe containing 30 μl of 3.8% trisodium citrate was used to draw ˜300 μl blood by a single puncture of the left ventricle. Otherwise ˜170 μl of blood was collected, during tail tissue collection, in tubes containing 10 μl of 3.8% trisodium citrate. Plasma was prepared by two sequential centrifugations then frozen on liquid N2 and stored at −80° C. For determination of 3-OST-1 activity, 70 μl of fresh plasma was combined with 0.91 μl of 77 μg / ml pepstatin, 770 μg / ml leupeptin, 150 μg / ml aprotinin (Sigma, St. Louis, Mo.), and 77 mM PEFABLOC® SC (Boehringer Mannheim, Mannhei...
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