Product Catalog

• Structural and expression studies of RNA molecules
• Generating full-length cDNAs
• Isolation and characterization of 5' or 3' ends from low-copy RNA messages
• Amplification and further cloning of rare mRNAs
• Use in conjunction with exon-trapping methods
• Products of the RACE reaction can be directly sequenced without cloning

• Robust performance:
  Recombinant Transcriptor Reverse Transcriptase allows procession through regions of difficult secondary RNA structure.
• Convenient:
  Function and expression studies of either 5' or 3' end of the RNA can be performed with the same kit.
• Reliable:
  dA tailing of cDNA with Recombinant Terminal Transferase decreases the likelihood of inappropriate truncation.
• Reproducible:
  Oligo dT-anchor primer with non 3'dT ensures correct binding to the inner end of the poly (A) tail.
• Produce long fragments:
  Generate cDNA up to 14 kb in length with Transcriptor Reverse Transcriptase.

Obtaining a full-length cDNA is of critical importance for structural and expression studies. The amplification of DNA sequences from a messenger RNA template between a defined internal site and unknown sequences of either the 3' or the 5' end of the mRNA are often referred to as RACE (rapid amplification of cDNA ends), “anchored” PCR, or “one-sided” PCR. Transcriptor Reverse Transcriptase is supplied with the kit to transcribe full-length cDNA up to 14 kb in length and, due to the thermostability of Transcriptor Reverse Transcriptase (up to 65°C), to work with GC-rich templates with high secondary structure. In addition, with Transcriptor Reverse Transcriptase, high sensitivity can be achieved. This results in highly efficient cDNA synthesis and the generation of long RACE products.
Purification of the first-strand cDNA is performed with the High Pure PCR Product Purification Kit. Recombinant Terminal Transferase is used to add a homopolymeric A-tail to the 3' end of the cDNA. The use of poly(A) tail decreases the likelihood of inappropriate trunction by the oligo dT-anchor primer, and due to the weaker A/T binding compared to the G/C binding, longer stretches of A residues are required before the oligo dT-anchor primer will bind to an internal site and truncate the amplification product.
Tailed cDNA is amplified by PCR using a gene-specific primer and the oligo dT-anchor primer. The obtained cDNA is further amplified by a second PCR using a nested specific primer and the PCR anchor primer. As a result, the RACE products can be cloned into an appropriate vector for subsequent characterization studies.
 

1. cDNA Synthesis Buffer, 5x conc. (100 μl)
2. Transcriptor Reverse Transcriptase (10 μl)
3. Deoxynucleotide Mix, each dNTP present at 10 mM in Tris-HCl, pH 7.5 (50 μl)
4. dATP, 2 mM in Tris-HCl, pH 7.5 (30 μl)
5. Reaction Buffer, 10x conc. (1000 μl)
6. Terminal Transferase, recombinant (10 μl)
7. Control neo-RNA (20 μl)
8. Oligo(dT) Anchor Primer (40 μl)
9. PCR Anchor primer (40 μl)
10. Control Primer, neo1/rev (40 μl)
11. Control Primer, neo2/rev (40 μl)
12. Control Primer, neo3/for (40 μl)

Associated Products

• Rapid DNA Ligation Kit;
• Transcriptor Reverse Transcriptase;
  A recombinant reverse transcriptase for the robust transcription of RNA fragments up to 14 kb
• PCR Nucleotide Mix;
  Premixed solution of highly pure PCR-grade nucleotides (dATP, dGTP, dCTP and dTTP, each at a concentration of 10 mM)
• PCR Nucleotide Mix^PLUS;
  Premixed deoxynucleotide solution for use in PCR and RT-PCR carryover prevention
• FastStart High Fidelity PCR System;
  Blend of FastStart Taq DNA Polymerase and a thermostable proofreading protein for high fidelity hot start PCR of DNA fragments up to 5 kb
• FastStart High Fidelity PCR System, dNTPack;
  FastStart High Fidelity Enzyme Blend with ready-to-use PCR-Grade Nucleotide Mix
• Deoxynucleoside Triphosphate Set;
  PCR Grade, Na-Salt
• Protector RNase Inhibitor;
  from rat lung, recombinant
• mRNA Isolation Kit;
  For isolation of at least 70 μg of poly (A+) RNA
• mRNA Capture Kit;
  Immobilizes poly (A+) RNA within a 0.2 ml PCR tube
• High Pure RNA Isolation Kit;
  For small-scale (mini) preparations of purified and intact total RNA
• High Pure RNA Tissue Kit;
  For the isolation of total RNA from tissue