Fig. 8.
Fig. 8. hIAN1 mRNA expression pattern. / (A) Expression of hIAN1 mRNA in various human tissues. Clontech poly A+ Multiple Tissues Blot was hybridized with an hIAN1 probe. Each lane contains 2 μg poly A+ RNA. Lane 1, spleen; lane 2, thymus; lane 3, prostate; lane 4, testis; lane 5, ovary; lane 6, small intestine; lane 7, colon; lane 8, peripheral blood lymphocytes. The amounts of RNA loaded and transferred to the membrane were assessed by a GAPDH hybridization. (B) Expression of hIAN1 mRNA in mature hematopoietic cells. RT-PCR analysis of hIAN1 mRNA expression was performed on B lymphocytes (lane 1), T lymphocytes (lane 2), mature erythroid cells (lane 3), mature myeloid cells (lane 4), and mature megakaryocytic (lane 5) cells. Jurkat and Jurkat-ΔCOOH cells (lanes 6 and 7) were used as controls. The amount of cDNA used for PCR was normalized relative to the levels of the S14 gene product.

hIAN1 mRNA expression pattern.

(A) Expression of hIAN1 mRNA in various human tissues. Clontech poly A+ Multiple Tissues Blot was hybridized with an hIAN1 probe. Each lane contains 2 μg poly A+ RNA. Lane 1, spleen; lane 2, thymus; lane 3, prostate; lane 4, testis; lane 5, ovary; lane 6, small intestine; lane 7, colon; lane 8, peripheral blood lymphocytes. The amounts of RNA loaded and transferred to the membrane were assessed by a GAPDH hybridization. (B) Expression of hIAN1 mRNA in mature hematopoietic cells. RT-PCR analysis of hIAN1 mRNA expression was performed on B lymphocytes (lane 1), T lymphocytes (lane 2), mature erythroid cells (lane 3), mature myeloid cells (lane 4), and mature megakaryocytic (lane 5) cells. Jurkat and Jurkat-ΔCOOH cells (lanes 6 and 7) were used as controls. The amount of cDNA used for PCR was normalized relative to the levels of the S14 gene product.

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