Fig. 2.
Fig. 2. Analysis of the chemokine receptor transcripts expressed in freshly isolated thymocytes. / Total RNA extracted from thymi and spleen from CCR9-deficient and wild-type mice were analyzed by multiprobe ribonuclease protection assay using a mCR-5 RiboQuant mouse template set (BD Pharmingen). The autoradiogram shows the mCR-5–probe set not treated with RNases (lane 1), and the RNase-protected bands following hybridization with control yeast tRNA (line 2) with RNA isolated from CCR9-deficient (lane 3), or wild-type thymi (lane 4). Also shown are the RNase-protected bands obtained after hybridization with RNA isolated from CCR9-deficient spleens (lane 5), or wild-type spleens (lane 6). The identity of the various protected bands is indicated on the left.

Analysis of the chemokine receptor transcripts expressed in freshly isolated thymocytes.

Total RNA extracted from thymi and spleen from CCR9-deficient and wild-type mice were analyzed by multiprobe ribonuclease protection assay using a mCR-5 RiboQuant mouse template set (BD Pharmingen). The autoradiogram shows the mCR-5–probe set not treated with RNases (lane 1), and the RNase-protected bands following hybridization with control yeast tRNA (line 2) with RNA isolated from CCR9-deficient (lane 3), or wild-type thymi (lane 4). Also shown are the RNase-protected bands obtained after hybridization with RNA isolated from CCR9-deficient spleens (lane 5), or wild-type spleens (lane 6). The identity of the various protected bands is indicated on the left.

Close Modal

or Create an Account

Close Modal
Close Modal