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. Author manuscript; available in PMC: 2011 Jan 1.

Published in final edited form as: Cell Immunol. 2010;266(1):24–31. doi: 10.1016/j.cellimm.2010.08.007

Fig. 1 — (A) Schematic representation of the wild type (WT) and targeted (KO) Fcrlb alleles. A detailed description of the targeting vector can be found in Fig. S1. Primers used for RT-PCR analysis of Fcrlb mRNA expression are illustrated by arrowheads. (B) RT-PCR analysis of Fcrlb gene expression in splenic B cells. Three different forward (FW) primers in conjunction with a common reverse (RV) primer were used in RT-PCR analysis of Fcrlb expression in purified splenic B cells from WT and KO mice. The expected sizes of the PCR products are indicated.

Fig. 1 — (A) Schematic representation of the wild type (WT) and targeted (KO) Fcrlb alleles. A detailed description of the targeting vector can be found in Fig. S1. Primers used for RT-PCR analysis of Fcrlb mRNA expression are illustrated by arrowheads. (B) RT-PCR analysis of Fcrlb gene expression in splenic B cells. Three different forward (FW) primers in conjunction with a common reverse (RV) primer were used in RT-PCR analysis of Fcrlb expression in purified splenic B cells from WT and KO mice. The expected sizes of the PCR products are indicated.