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. 1999 Aug 1;104(3):309–316. doi: 10.1172/JCI7016

Figure 1.

Figure 1

Construction of hBLTR transgene and screening of hBLTR TG mice. (a) Illustration of the pGL-CD11b-hBLTR construct. Restriction sites used for cloning, and sense (right-facing arrows) and antisense (left-facing arrows) primers used for PCR, are indicated. Nucleotide sequences of the primers corresponding to the hBLTR are underlined. (b) pGL-CD11b-hBLTR and mock (pGL) plasmids were transiently transfected into HEK293 cells, and intracellular calcium was mobilized by addition of LTB4 (100 nM). Genomic DNA isolated from potential founder mice (c) and F1 generations (d) were analyzed by PCR using primers specific for the CD11b-hBLTR transgene construct. Molecular sizes of expected PCR products are indicated by arrows.