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Invitrogen™ Anchored Oligo(dT)20 Primer
Description
Anchored Oligo(dT)20 Primer is a primer mixture consisting of a string of 20 deoxythymidylic acid residues followed by dV (dG, dA, or dC) and then by dN (dA, dT, dG, or dC). Due to the variable end-sequence, the primer is anchored to the 5´-end of the poly(A) tail of mRNA and prevents priming within the poly(A) tail.
Anchored Oligo(dT)20 Primer is recommended for use in cDNA labeling protocols and in RT-PCR. It is commonly used for first-strand cDNA systhesis.
Quality control: This product is qualified in a first-strand cDNA synthesis reaction
Order Info
Shipping Conditions: Dry Ice
Specifications
Specifications
| Product Type | Primer |
| Content And Storage | • Anchored Oligo(dT)20 Primer in DEPC-treated water (20 μL at 2.5 μg/μL) Store at –20°C. Guaranteed stable for 6 months when properly stored. |
| 5'Primer Modification | Phosphate |
| Primer Length | 22-mer |
| Primer Sequence | 5'd PO4 [(T)20VN]3' |
| Purification Method | Gel-purified, Desalted |
| Shipping Condition | Dry Ice |
| Concentration | 2.5 μg/μL |
| Primer | Anchored Oligo dT Primer |
| Quantity | 20 μL |
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Frequently Asked Questions (FAQs)
Anchored Oligo(dT) primers have 2 random bases at the 3' end of the stretch of Ts. The first random base is either an A, G, or C, while the second can be any of the 4 standard nucleotides, i.e., A, T, G or C. The use of anchored oligo(dT) primers results in increased cDNA synthesis yields.
The choice of primer depends on your experimental goals. Oligo(dT) is recommended when using total RNA for cDNA synthesis. It is the key to full-length cDNA synthesis. Random hexamers give a series of short first-strand products spanning the entire mRNA. Use of random hexamers may be helpful if the PCR fragment is at the 5´ end of a large mRNA. To ensure full-length cDNA synthesis of large transcripts, oligo(dT) can be added along with random hexamers during first-strand synthesis. Gene-specific primers (GSP) for cDNA synthesis may also be used and are required in a few applications such as 5´ RACE and qRT-PCR. For GC-rich templates or templates rich in secondary structure, a GSP may not work as well as priming with oligo dT for first-strand synthesis. If an RT-PCR is problematic, trying different options of oligo dT, random primers and/or GSP for priming first-strand synthesis may resolve the issue. Oligo(dT)20 primer (Cat. No. 18418-020) is recommended for use with SuperScript III Reverse Transcriptase (Cat. no. 18080-044), ThermoScript Reverse Transcriptase (Cat. No. 12236-014), Thermo-X Reverse Trascriptase (Cat. No. 11150-025), and Cloned AMV Reverse Transcriptase (Cat. No. 12328-019).
Reference:
Frohman,M.A., Dush,M.K., Martin, G.R. (1988) Proc. Nat. Acad. Sci USA 85, 8998
For Research Use Only. Not for use in diagnostic procedures.