<result><Library><Item><Library_ID>51</Library_ID>
<Library_Name>Alpha-CT phage display library (XCCX3CX5C)</Library_Name>
<Library_Length>13</Library_Length>
<Library_Complexity>5.0e8</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>J. K. Scott (Simon Fraser University, Burnaby, Canada)</Library_From>
<Library_Randomness>Semi-random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Circular</Library_Topology>
<Comments>The library is based on vector f88-4 (GenBank Accession AF218363).</Comments>
</Item><Item><Library_ID>52</Library_ID>
<Library_Name>LX8 and X15CX phage display library pool</Library_Name>
<Library_Length>12, 17</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>J. K. Scott (Simon Fraser University, Burnaby, Canada)</Library_From>
<Library_Randomness>Semi-random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology></Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>53</Library_ID>
<Library_Name>X15 and X21 phage display library pool</Library_Name>
<Library_Length>15, 21</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Anthony J. Conley</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>54</Library_ID>
<Library_Name>CX12C phage display library</Library_Name>
<Library_Length>12</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Tel-Aviv University (TAU)</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Circular</Library_Topology>
<Comments>The library is based on the fth-1 expression vector in which random peptides are recombinantly fused to the NH2 terminus of a recombinant protein VIII of the fd filamentous bacteriophage.</Comments>
</Item><Item><Library_ID>55</Library_ID>
<Library_Name>f3-6mer and J404-3 phage display library pool</Library_Name>
<Library_Length>6, 9</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From></Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>Library f3-6mer (GenBank Accession AF246446) is based on vector fUSE5, which displys its guest peptides on all five copies of the minor coat protein pIII at one tip of the virion. The library is also known as fUSE/6mer. </Comments>
</Item><Item><Library_ID>56</Library_ID>
<Library_Name>CX6C phage display library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Igor Fisch</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Circular</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>57</Library_ID>
<Library_Name>X6 phage display library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Igor Fisch</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>58</Library_ID>
<Library_Name>X4[RK]X3 phage display library</Library_Name>
<Library_Length>7</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Richard L. Stevens</Library_From>
<Library_Randomness>Semi-random</Library_Randomness>
<Library_Scheme>NNN</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>Phage display peptide library is tryptase specific. The genome of the Ff bacteriophage consists of the 11 genes designated gI to gXI. Although the protein (pIII) encoded by gIII is chymotrypsin-, thermolysin-, and subtilisin-susceptible, it is trypsin-resistant. Thus, phage display peptide libraries can give insight into the substrate specificities of certain proteases.</Comments>
</Item><Item><Library_ID>59</Library_ID>
<Library_Name>L100 phage display library (X10)</Library_Name>
<Library_Length>10</Library_Length>
<Library_Complexity>6.0e8</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Matthew D. Scharff (Einstein College, New York)</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>L100 is based on fUSE5.</Comments>
</Item><Item><Library_ID>60</Library_ID>
<Library_Name>CX9C phage display library</Library_Name>
<Library_Length>9</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>C. Richter King</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Circular</Library_Topology>
<Comments>The library was constructed to contain a variable 9-amino acid peptide flanked by cysteine residues inserted into the GeneIII protein of the phage fUSE5.</Comments>
</Item><Item><Library_ID>61</Library_ID>
<Library_Name>S-(X)5-FRW-(X)4 phage display library</Library_Name>
<Library_Length>9</Library_Length>
<Library_Complexity>1.0e5</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Jarl E. S. Wikberg</Library_From>
<Library_Randomness>Semi-random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>A small library was constructed to test this phage display system using a partially randomized oligonucleotide (MS-5pcr) that kept the MSH-core sequence Phe7-Arg8-Trp9, which is believed to be most essential for receptor binding, to direct phage binding toward the receptors. The Ser at the junction with the pelB leader sequence was also maintained to reduce the amount of sequences that may not be processed by the leader peptidase.</Comments>
</Item><Item><Library_ID>62</Library_ID>
<Library_Name>Cys6 phage display library (CX6C)</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>2.2e7</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>T. E. Michaelsen</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Circular</Library_Topology>
<Comments>The library present peptides of six random amino acids constrained by flanking cysteines were created by insertion of double-stranded oligonucleotides between the Sfi1 site of the vector fUSE5, providing the gene 3 protein (g3p) final amino acid sequences NH2-ADGACX6CGAA-g3p for the hexamer library (cys6), where X stands for any amino acid.</Comments>
</Item><Item><Library_ID>63</Library_ID>
<Library_Name>Cys9 phage display library (CX9C)</Library_Name>
<Library_Length>9</Library_Length>
<Library_Complexity>5.5e7</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>T. E. Michaelsen</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Circular</Library_Topology>
<Comments>The library present peptides of nine random amino acids constrained by flanking cysteines were created by insertion of double-stranded oligonucleotides between the Sfi1 site of the vector fUSE5, providing the gene 3 protein (g3p) final amino acid sequences ADGACX9CGAA-g3p for the nanomer library (cys9), where X stands for any amino acid.</Comments>
</Item><Item><Library_ID>64</Library_ID>
<Library_Name>X9 phage display library</Library_Name>
<Library_Length>9</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Heimo Breiteneder</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>Random peptides are displayed on filamentous phage as fusion to the NH2 terminus of the major coat protein pVIII.</Comments>
</Item><Item><Library_ID>65</Library_ID>
<Library_Name>X15 phage display library</Library_Name>
<Library_Length>15</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Michael Jaye</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>A fusion phage display library was constructed in the filamentous bacteriophage fuse 5B, a vector derived from fd filamentous phage. The fuse5B vector was constructed from the vector fuse5 by removal of an existing BstXI site in fuse5 followed by replacement of the SfiI cloning sites with BstXI cloning sites.</Comments>
</Item><Item><Library_ID>66</Library_ID>
<Library_Name>GX6G phage display library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>2.5e9</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Zoller and Smith</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>67</Library_ID>
<Library_Name>X6PPIP phage display library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>2.0e9</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Zoller and Smith</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>68</Library_ID>
<Library_Name>RSLRPLX6 phage display library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>5.8e8</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Zoller and Smith</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>69</Library_ID>
<Library_Name>PPPYPPX6 phage display library </Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>3.1e8</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Zoller and Smith</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>70</Library_ID>
<Library_Name>RKRSHRXXPPPXXXVQ phage display library</Library_Name>
<Library_Length>5</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Christian Freund</Library_From>
<Library_Randomness>Semi-random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>Sequences of the focused library RKRSHRXXPPPXXXVQ were cloned into PC89. PC89 was a gift from Gianni Cesareni(Dipartimento di Biologia, Universita di Roma).</Comments>
</Item><Item><Library_ID>71</Library_ID>
<Library_Name>X9 phage display library</Library_Name>
<Library_Length>9</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Gianni Cesareni(Dipartimento di Biologia, Universita di Roma)</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>72</Library_ID>
<Library_Name>X10 phage display library</Library_Name>
<Library_Length>10</Library_Length>
<Library_Complexity>1.0e8</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Daniel Baty</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>73</Library_ID>
<Library_Name>X12 phage display library</Library_Name>
<Library_Length>12</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Peptide Door, Japan</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>74</Library_ID>
<Library_Name>X6 phage display library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>1.0e7</Library_Complexity>
<Library_Titer>5.4e8</Library_Titer>
<Library_From>Michael N. Margolies</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>A bacteriophage-displayed library contains randomized mutations at H chain residues 30-35 of the anti-digoxin antibody 26-10 Fab.</Comments>
</Item><Item><Library_ID>75</Library_ID>
<Library_Name>AA-xxxxx-AA phage display library</Library_Name>
<Library_Length>5</Library_Length>
<Library_Complexity>2.0e6</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>James A. Wells</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item></Library></result>