Table 1.

Oligonucleotide Probes Used in EMSAs

Name Sequence 5′3′
Irrelevant probe 
Irr.  GGAAGCAGACCACGTGGTCTGCTTCC  
Probes for Sp1 region-150 
MS6  TCCCCTCCCCTCCCCTCC  
MS7 CCGTTGCGTCCCACCCACCGCGT  
mMS7 CCGTTGCGTCCCAttCACCGCGT  
Probes for megakaryocytic cell-specific activity region 
 −126−115−108 −90 
  ‖‖‖‖  
MSPw   CGGAGGGGAGGAAGCGCGAGTCCGCG  
Pw  CTAGAGAAGCCGGAGGGGAGGAAGCGC  
mPw1  CTAGAGAAGCCGGcGttGAGGAAGCGC  
mPw2  CTAGAGAAGaCtGAGGGGAGGAAGCGC  
Pws  AAGCCGGAGGGGAGG  
MS4  AGGGGAGGAAGCGCGAGTCC  
mMS4  AGGGGcGtcAGCGCGAGTCC 
Name Sequence 5′3′
Irrelevant probe 
Irr.  GGAAGCAGACCACGTGGTCTGCTTCC  
Probes for Sp1 region-150 
MS6  TCCCCTCCCCTCCCCTCC  
MS7 CCGTTGCGTCCCACCCACCGCGT  
mMS7 CCGTTGCGTCCCAttCACCGCGT  
Probes for megakaryocytic cell-specific activity region 
 −126−115−108 −90 
  ‖‖‖‖  
MSPw   CGGAGGGGAGGAAGCGCGAGTCCGCG  
Pw  CTAGAGAAGCCGGAGGGGAGGAAGCGC  
mPw1  CTAGAGAAGCCGGcGttGAGGAAGCGC  
mPw2  CTAGAGAAGaCtGAGGGGAGGAAGCGC  
Pws  AAGCCGGAGGGGAGG  
MS4  AGGGGAGGAAGCGCGAGTCC  
mMS4  AGGGGcGtcAGCGCGAGTCC 

The indicated sequences represent the double-stranded probe resulting after annealing of sense and antisense oligonucleotides, followed by a fill-in reaction. Probes are aligned when appropriate. Mutant sequences are indicated by bold lowercase letters. The position of the sequences relative to the transcription start site is shown for the last group of probes.

F0-150

The Sp1 consensus binding site in MS7 is underlined.

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