The f3TR1 15-mer peptide phage display library is built from the
f3TR1 filamentous phage vector (HM355479.1) by replacing a synthetic 14 bp stuffer sequence with frame-restoring 45 bp random oligo nucleotides. The 15-mer foreign peptide insert is expressed on pIII as a fusion to the N-terminus of pIII through a trypsin-recognition sequence. The f3TR1 phage display library maintains
E. coli infectivity and does not require a helper phage for assembly and release of virions.
Product | Peptide phage display library |
---|---|
Cat. Number | COPD0002 |
Type | pIII |
Format | 15-mer linear |
Diversity | 1.91x10^10 |
Clone copies | >100 |
Excluded codons | Stop and cysteine |
Elution | Trypsin digestion, disruption of non-covalent interactions |
Bacterial resistance | Tetracycline (20 μg/mL) |
Growth strains | K91BluKan |
Reference | Scott JK et al. Science. 1990 Jul 27;249(4967):386-90. doi: 10.1126/science. |
Price | $4950.00 |
Certificate of Analysis | COA-COPD0002 |
The f3TR1 vector was created by Dr. George Smith at the University of Missouri and the f3TR1 linear 15-mer library was created by Cell Origins (#COPD0002).
Thomas WD, Golomb M, Smith GP. Corruption of phage display libraries by target-unrelated clones: diagnosis and countermeasures. Anal Biochem. 2010 Dec 15;407(2):237-40. doi: 10.1016/j.ab.2010.07.037.
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