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Invitrogen™ TA Cloning™ Kit, with pCR™2.1 Vector, without competent cells
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No. of Reactions:
20 Reactions
40 Reactions
Unit Size:
Each
Description
The TA Cloning Kit uses the pCR2.1 cloning vector and ExpressLink T4 DNA Ligase to generate a ligation product in a fifteen-minute, room-temperature ligation step. Reactions typically yield >80% recombinants containing inserts.
- Fast and convenient: 15-minute, room-temperature ligation
- Efficient: blue/white screening and >80% clones with correct insert
- Flexible: choice of kanamycin or ampicillin resistance for flexible antibiotic selection
- Hassle-free: eliminates any enzymatic modifications of the PCR product
- Streamlined: does not require the use of PCR primers that contain restriction sites
- Provides 3'-T overhangs for direct ligation of Taq-amplified PCR products
- T7 promoter for in vitro RNA transcription and sequencing
- Versatile polylinker with flanking EcoR I sites for easy excision of insert
- M13 forward and reverse primer sites for sequencing
- How TA Cloning Works
- Taq polymerase has non-template-dependent activity that adds single deoxyadenosine (A) to 3' ends of PCR products
- Linearized vector supplied in this kit has single 3' deoxythymidine (T) residues
- Allows PCR inserts to ligate efficiently with vector
Cloning, PCR Cloning

Specifications
Specifications
Bacterial or Yeast Strain | Not Included |
Cloning Method | TA Cloning |
Content And Storage | TA Cloning™ kits contain linearized pCR™2.1 vector, ExpressLink™ T4 DNA ligase, 5X ExpressLink™ T4 DNA ligation buffer, dNTPs, 10X PCR buffer, sterile water, and controls. Store all components at -20°C. All reagents are guaranteed stable for 6 months when properly stored. |
Format | Kit |
For Use With (Application) | PCR Cloning |
No. of Reactions | 20 Reactions |
Product Line | TA Cloning™ |
Product Type | Cloning Kit |
Promoter | T7 |
Quantity | 20 reactions |
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For Research Use Only. Not for use in diagnostic procedures.
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Invitrogen™ TA Cloning™ Kit, with pCR™2.1 Vector, without competent cells >
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