Gateway™ pENTR™ 11 Dual Selection Vector

Catalog number:  A10467

 Related applications:

Gateway Cloning

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Gateway® entry vectors are designed to clone DNA sequences using restriction endonucleases and ligase to create a Gateway® entry clone. The resulting entry clone is ready for recombination with a destination vector to create an expression clone. New: pENTR™ Dual Selection vectors!

The Gateway® entry vectors (Table 1) offer the following:
• attL1 and attL2 sites for site-specific recombination of the entry clone with a Gateway® destination vector to ensure cloning of the gene of interest in the correct orientation for expression
• Kozak consensus sequence for efficient translation initiation in eukaryotic systems
• Ribosome binding site for efficient translation initiation in prokaryotic systems (pENTR™ 1A Dual Selection, pENTR™3C Dual Selection, and pENTR™11 Dual Selection vectors only)
• rrnB transcription termination sequences to prevent basal expression of the PCR product of interest in E. coli
• pUC origin for high-copy replication and maintenance of the plasmid in E. coli
• Kanamycin resistance gene for selection in E. coli
• The ccdB⁄chloramphenicol fusion gene located between the two attL sites for
o negative selection and
o Chloramphenicol selection in E. coli
• Kanamycin resistance gene for selection in E. coli


Vector Type: pENTR
Cloning Method: Gateway®
Antibiotic Resistance (Bacterial): Chloramphenicol (CmR), Kanamycin (KanR)
Cleavage: No Cleavage Site
Product Line: pENTR™
Product Size: 10 µg
Protein Tag or Fusion: Untagged
Regulatory Statement: For Research Use Only. Not for use in diagnostic procedures.

Contents & storage

10 µg pENTR™ Dual Selection vector, in 20 ul in TE buffer, pH 8.0.
Store at -20°C


Manuals & protocols