1. Scheme 1 Chemical structures of DMT- BM (LEV) BCE and DMT- CM2 (Bz ₂ ) BCE.
From: Chemical synthesis and characterization of branched oligodeoxyribonucleotides (bDNA) for use as signal amplifiers in nucleic acid quantification assays
Nucleic Acids Res. 1997;25(23): doi: /nar/
Nucleic Acids Res | © 1997 Oxford University Press

2. Figure 5 Characterization of 15×3 bAM by HPCE (with co-injection of a purified bAM containing five 60mer sequences).
From: Chemical synthesis and characterization of branched oligodeoxyribonucleotides (bDNA) for use as signal amplifiers in nucleic acid quantification assays
Nucleic Acids Res. 1997;25(23): doi: /nar/
Nucleic Acids Res | © 1997 Oxford University Press

3. Figure 1 ( A ) Standard 15× bDNA comb oligomer
Figure 1 ( A ) Standard 15× bDNA comb oligomer. ( B ) 15× bDNA comb oligomer containing CM2 .
From: Chemical synthesis and characterization of branched oligodeoxyribonucleotides (bDNA) for use as signal amplifiers in nucleic acid quantification assays
Nucleic Acids Res. 1997;25(23): doi: /nar/
Nucleic Acids Res | © 1997 Oxford University Press

4. Figure 4 Branched amplification multimer (bAM) assembled by enzymatic ligation. The ligation sites are indicated by ^.
From: Chemical synthesis and characterization of branched oligodeoxyribonucleotides (bDNA) for use as signal amplifiers in nucleic acid quantification assays
Nucleic Acids Res. 1997;25(23): doi: /nar/
Nucleic Acids Res | © 1997 Oxford University Press

5. Figure 6 Characterization of 15×3 bAM by BODIPY FL hybridization-dependent quenching. ( A ) Fluorescence of free oligomer-3′-BODIPY FL. ( B ) Fluorescence of oligomer-3′-BODIPY FL hybridized to 15×3 bAM.
From: Chemical synthesis and characterization of branched oligodeoxyribonucleotides (bDNA) for use as signal amplifiers in nucleic acid quantification assays
Nucleic Acids Res. 1997;25(23): doi: /nar/
Nucleic Acids Res | © 1997 Oxford University Press

6. Figure 7 Melting curves of AP probe versus complements: ( 1 ) AP probe/1 site complement; ( 2 ) AP probe/3 site complement; ( 3 ) AP probe/15×3 bAM.
From: Chemical synthesis and characterization of branched oligodeoxyribonucleotides (bDNA) for use as signal amplifiers in nucleic acid quantification assays
Nucleic Acids Res. 1997;25(23): doi: /nar/
Nucleic Acids Res | © 1997 Oxford University Press

7. Figure 2 Characterization of 15× bDNA comb oligomer
Figure 2 Characterization of 15× bDNA comb oligomer. ( A ) HPCE after linear synthesis. ( B ) HPCE after branched synthesis.
From: Chemical synthesis and characterization of branched oligodeoxyribonucleotides (bDNA) for use as signal amplifiers in nucleic acid quantification assays
Nucleic Acids Res. 1997;25(23): doi: /nar/
Nucleic Acids Res | © 1997 Oxford University Press

8. Figure 3 Characterization of 15× bDNA comb oligomer containing CM2
Figure 3 Characterization of 15× bDNA comb oligomer containing CM2 . HPCE after periodate cleavage.
From: Chemical synthesis and characterization of branched oligodeoxyribonucleotides (bDNA) for use as signal amplifiers in nucleic acid quantification assays
Nucleic Acids Res. 1997;25(23): doi: /nar/
Nucleic Acids Res | © 1997 Oxford University Press