Fig. 1.
![Fig. 1. Differential mRNA display of Mm subline cells. Total RNA isolated from Mm-A, Mm-P, Mm-S1, and Mm-S2 cells was reverse transcribed and amplified by PCR in the presence of [35S]dATP. AP-15 (5′-AGGGCCTGTT-3′ ) was used as an arbitrary primer and T12MT (A) or T12MC (B) was used as an anchored oligo(dT) primer. The PCR fragments were displayed on a 6% DNA sequencing gel and autoradiogrammed as detailed in the Materials and Methods. Fragments 15T01 (A) and 15C01 (B) are indicated by arrows.](https://ash.silverchair-cdn.com/ash/content_public/journal/blood/89/8/10.1182_blood.v89.8.2975/4/bl_0008f1.jpeg?Expires=1743078700&Signature=Jr21ugMqlDhjTyyARzcAdRPJm6vVlLcTAwuQKoQA~ts4g2EYiCr2BdJyF0CFGm5y-7ShoCvhwI9SHcOw8I237HboZJYV3tEm1UQdV2W1aTIWBhVjbYjYySNoXGs3q4Uv5VSB3KzsMtbF5buPCD~O4jiWd2KWfFzW-ZO~2HNHzqHHq9FgN0~a5ugIGdFfJ2pmwzxoTCm98J-pyVwv9kHT6cDhcOhmfovIkFCwmPBzl65XeIZcbQjc3eP0urg0dQICoDrLyIXxW22RLXqF9j9rBXdisbukli9fb7GnvIp0V7kIkwTuTcz-nK~ijgEsnSFbVmdnAalVTw7e4zImOpHbCw__&Key-Pair-Id=APKAIE5G5CRDK6RD3PGA)
Differential mRNA display of Mm subline cells. Total RNA isolated from Mm-A, Mm-P, Mm-S1, and Mm-S2 cells was reverse transcribed and amplified by PCR in the presence of [35S]dATP. AP-15 (5′-AGGGCCTGTT-3′ ) was used as an arbitrary primer and T12MT (A) or T12MC (B) was used as an anchored oligo(dT) primer. The PCR fragments were displayed on a 6% DNA sequencing gel and autoradiogrammed as detailed in the Materials and Methods. Fragments 15T01 (A) and 15C01 (B) are indicated by arrows.
