Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : RTSZ-01
| Cat. No. | RTSZ-01 |
| Description | Unlike mRNAs, small RNAs lack poly-A tails. Therefore, cloning small RNA molecules begins with ligation of adaptors to the 5′ and 3′ ends of small RNAs followed by reverse transcription and PCR amplification. This kit contains all of the reagents necessary for the isolation, cDNA synthesis, and amplification steps that allow cloning of small (18-26 bases) RNA molecules (including microRNAs). |
| Sample Type | RNA |
| Report Gene | Small RNAs to cDNA |
| Features | Efficient cDNA synthesis from small RNAs (18-26 bases) |
| Applications |
•Small RNA cloning for preparing small RNA libraries •Real-Time PCR •cDNA can be used for TA cloning and small RNA library generation |
| Selection Marker | RNA |
| Storage | Package with enzyme should be stored at -20°C, others can be stored at 4°C. |
| Shipping | Dry ice |
A: This kit contains all of the reagents necessary for the isolation, cDNA synthesis, and amplification steps that allow cloning of small (18-26 bases) RNA molecules (including microRNAs).
A: Cloning and analyzing small RNA molecules is one method used to assess their expression patterns. Unlike mRNAs, small RNAs lack poly-A tails. Therefore, cloning small RNA molecules involves ligation of RNA or RNA/DNA chimeric adaptors to the 5’ and 3’ ends of extracted small RNAs followed by reverse transcription and then PCR.
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By using magnetic beads, this kit provides a simplified workflow that does not require gel extraction of nucleic acids after adaptor ligation. Therefore, small RNA-derived cDNAs can be amplified by a simple procedure. The amplified cDNA can then be used directly for TA cloning.
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