![How would one work out the Tm value for a single primer? What is the Tm value for this primer sequence? 5'-GCCAGTCAAACAGTCAGTAA-3' B. ~47oC C. ~50oC D. ~53oC E. ~56oC : r/a:t5_318cy How would one work out the Tm value for a single primer? What is the Tm value for this primer sequence? 5'-GCCAGTCAAACAGTCAGTAA-3' B. ~47oC C. ~50oC D. ~53oC E. ~56oC : r/a:t5_318cy](https://external-preview.redd.it/wF4MLnRL12_90I71Zx1wWdRIoI2s-vIYa8MQSETa85k.jpg?width=640&crop=smart&auto=webp&s=08fab9e34c1ad97a31d610b2709f6f30540100e0)
How would one work out the Tm value for a single primer? What is the Tm value for this primer sequence? 5'-GCCAGTCAAACAGTCAGTAA-3' B. ~47oC C. ~50oC D. ~53oC E. ~56oC : r/a:t5_318cy
![Primer design strategy for denaturation bubble-mediated strand exchange amplification - ScienceDirect Primer design strategy for denaturation bubble-mediated strand exchange amplification - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S0003269719312813-fx1.jpg)
Primer design strategy for denaturation bubble-mediated strand exchange amplification - ScienceDirect
![SOLVED: QNo.3. Calculate Tm of the following primers Gene: Sequence Melting temperature Forward primer TCGAGTCGCGTCCACC Reverse primer GGGAGCATCGTCGCCC Amplified product length = b. Screen shot of in-silico PCR= Cytogenetic location= d. Targeted SOLVED: QNo.3. Calculate Tm of the following primers Gene: Sequence Melting temperature Forward primer TCGAGTCGCGTCCACC Reverse primer GGGAGCATCGTCGCCC Amplified product length = b. Screen shot of in-silico PCR= Cytogenetic location= d. Targeted](https://cdn.numerade.com/ask_images/479db41e130a4d759330f82f59f9f3f4.jpg)