<p>(A) 5′ and 3′ rapid amplification of cDNA ends (RACE) was performed using RNA isolated from infected NIH3T12 fibroblasts and stimulated MHV68 infected A20-HE2 cells. The number of RACE clones that were identified for transcript initiation and termination sites are summarized. (B) A diagram of the transcript initiation and termination sites is shown with the genomic coordinates.</p
<p>Total RNA from human HEK293 fibroblasts, mouse 3T3-L1 preadipocytes and rat placenta was used as ...
Rapid amplification of cDNA ends (RACE) is a widely used approach for transcript identification. Ran...
<p>The assays were conducted in U2OS cells that were transiently transfected with the HPV18 genome (...
<p>(A) miR173-mediated cleavage of miR173ts_CHS transcripts. The cleavage position and the number of...
Determination of transcription initiation sites has commonly been performed by primer extension and ...
<p>Arrows indicate the 5’ ends of mRNA fragments, as identified by cloned 5’ RLM-RACE products, with...
Rapid amplification of cDNA ends (RACE) is a powerful PCR-based technique for determination of RNA t...
<p>Arrows indicate the inferred cleavage sites and numbers above represent the fractions of cloned 5...
<p>A) For transcript ncINT1Ms2, a single product of 370 bp was obtained with 3′-RACE. After transcri...
<p>The cleavage sites and the number of sequenced clones corresponding to each site are indicated by...
<p>The arrows indicate the cleavage sites and the numbers show the frequency of clones sequenced.</p
<p>Boxes indicate the cleavage sites; the numbers indicate the fraction of cloned PCR products termi...
Rapid amplification of cDNA ends (RACE) is a widely used approach for transcript identification. Ran...
Rapid Amplification of cDNA Ends (RACE) is a technique used in molecular biology to obtain full leng...
<p>Agarose gel image of 5′ RACE products (A) and the target mRNA cleavage sites (B). The targeted mR...
<p>Total RNA from human HEK293 fibroblasts, mouse 3T3-L1 preadipocytes and rat placenta was used as ...
Rapid amplification of cDNA ends (RACE) is a widely used approach for transcript identification. Ran...
<p>The assays were conducted in U2OS cells that were transiently transfected with the HPV18 genome (...
<p>(A) miR173-mediated cleavage of miR173ts_CHS transcripts. The cleavage position and the number of...
Determination of transcription initiation sites has commonly been performed by primer extension and ...
<p>Arrows indicate the 5’ ends of mRNA fragments, as identified by cloned 5’ RLM-RACE products, with...
Rapid amplification of cDNA ends (RACE) is a powerful PCR-based technique for determination of RNA t...
<p>Arrows indicate the inferred cleavage sites and numbers above represent the fractions of cloned 5...
<p>A) For transcript ncINT1Ms2, a single product of 370 bp was obtained with 3′-RACE. After transcri...
<p>The cleavage sites and the number of sequenced clones corresponding to each site are indicated by...
<p>The arrows indicate the cleavage sites and the numbers show the frequency of clones sequenced.</p
<p>Boxes indicate the cleavage sites; the numbers indicate the fraction of cloned PCR products termi...
Rapid amplification of cDNA ends (RACE) is a widely used approach for transcript identification. Ran...
Rapid Amplification of cDNA Ends (RACE) is a technique used in molecular biology to obtain full leng...
<p>Agarose gel image of 5′ RACE products (A) and the target mRNA cleavage sites (B). The targeted mR...
<p>Total RNA from human HEK293 fibroblasts, mouse 3T3-L1 preadipocytes and rat placenta was used as ...
Rapid amplification of cDNA ends (RACE) is a widely used approach for transcript identification. Ran...
<p>The assays were conducted in U2OS cells that were transiently transfected with the HPV18 genome (...