American Society of Hematology

Fig. 6.

$Fig. 6. Tissue distribution of ABP-276 and ABP-278 by RT-PCR. PCR products, amplified with primers P3 and P4 using various marathon cDNAs (Clontech) as templates, were fractionated on 1.5% agarose gel. The upper band (349 bp) represents the PCR products of ABP-278, while the lower band (277 bp) represents the PCR products of ABP-276. The difference in size is due to the presence and absence of the 72 bp exon sequence encoding the 24 amino acid Hinge I region. The PCR amplification of ABP-280 (P9 and P10) and G3PDH (P7 and P8) sequences were used as controls.$

Tissue distribution of ABP-276 and ABP-278 by RT-PCR. PCR products, amplified with primers P3 and P4 using various marathon cDNAs (Clontech) as templates, were fractionated on 1.5% agarose gel. The upper band (349 bp) represents the PCR products of ABP-278, while the lower band (277 bp) represents the PCR products of ABP-276. The difference in size is due to the presence and absence of the 72 bp exon sequence encoding the 24 amino acid Hinge I region. The PCR amplification of ABP-280 (P9 and P10) and G3PDH (P7 and P8) sequences were used as controls.

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