<result><Library><Item><Library_ID>126</Library_ID>
<Library_Name>ANL 22 phage display library</Library_Name>
<Library_Length>20</Library_Length>
<Library_Complexity>1e10</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Brian K. Kay</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>The ANL 22 library displayed X20 peptides as N-terminal fusions to the protein product of gene III of bacteriophage M13 using SAM vector.</Comments>
</Item><Item><Library_ID>127</Library_ID>
<Library_Name>Cys6 phage display library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>2.2e7</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Inger Sandlie</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Circular</Library_Topology>
<Comments>The Cys6 library was based on the vector fUSE5, which supports phage fd protein III (pIII) peptide expression.</Comments>
</Item><Item><Library_ID>128</Library_ID>
<Library_Name>Cys9 phage display library</Library_Name>
<Library_Length>9</Library_Length>
<Library_Complexity>5e7</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Inger Sandlie</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Circular</Library_Topology>
<Comments>The Cys9 library was based on the vector fUSE5, which supports phage fd protein III (pIII) peptide expression.</Comments>
</Item><Item><Library_ID>129</Library_ID>
<Library_Name>NNK11 phage display library</Library_Name>
<Library_Length>11</Library_Length>
<Library_Complexity>9e8</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Inger Sandlie</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>The NNK11 library was based on the vector fUSE5, which supports phage fd protein III (pIII) peptide expression.</Comments>
</Item><Item><Library_ID>130</Library_ID>
<Library_Name>Evo1 phage display library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>3e7</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Inger Sandlie</Library_From>
<Library_Randomness>Semi-random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Circular</Library_Topology>
<Comments>The Evo1 library was based on the vector fUSE5, which supports phage fd protein III (pIII) peptide expression. The insert sequence is XXXCPWFQWPCXXX, where X denotes any residue.</Comments>
</Item><Item><Library_ID>131</Library_ID>
<Library_Name>Evo2 phage display library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>3e7</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Inger Sandlie</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>The Evo2 library was based on the vector fUSE5, which supports phage fd protein III (pIII) peptide expression. The insert sequence is XXXXXXWFQWPC, where X denotes any residue.</Comments>
</Item><Item><Library_ID>132</Library_ID>
<Library_Name>Evo3 phage display library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>3e7</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Inger Sandlie</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>The Evo3 library was based on the vector fUSE5, which supports phage fd protein III (pIII) peptide expression. The insert sequence is CPWFQWPCXXXXXX, where X denotes any residue.</Comments>
</Item><Item><Library_ID>133</Library_ID>
<Library_Name>CPEP-8 phage display library (X3CX8CX3)</Library_Name>
<Library_Length>14</Library_Length>
<Library_Complexity>2e9</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>John Lund</Library_From>
<Library_Randomness>Semi-random</Library_Randomness>
<Library_Scheme>NNS</Library_Scheme>
<Library_Topology>Circular</Library_Topology>
<Comments>In the CPEP-8 library, peptides are displayed at the N-terminal of the pIII mature protein on the M13 bacteriophage surface.</Comments>
</Item><Item><Library_ID>134</Library_ID>
<Library_Name>fdMED1-based X6 phage display library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>2e8</Library_Complexity>
<Library_Titer>2e9</Library_Titer>
<Library_From></Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>135</Library_ID>
<Library_Name>Y-X10-M phage display library</Library_Name>
<Library_Length>10</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Ichio Shimada</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>This library displayed foreign peptides on the N terminus of the major coat protein (gVIII protein) of bacteriophage M13. Each foreign peptide has a 10-mer random sequence flanked by a Y residue (detectable residue at 280 nm by high-performance liquid chromatography) and a M residue (cyanogen bromide cleavage residue).</Comments>
</Item><Item><Library_ID>136</Library_ID>
<Library_Name>G-α phage display library (XXLXXXAX)</Library_Name>
<Library_Length>8</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer>8.4e3</Library_Titer>
<Library_From>V.A. Petrenko</Library_From>
<Library_Randomness>Semi-random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>G-α-library is a library of phages carrying b-galactosidase-binding peptide ADTFAKSMQ at the N-terminus of the pVIII protein surrounded by random amino acids.</Comments>
</Item><Item><Library_ID>137</Library_ID>
<Library_Name>fdMED1-based CX6C M13 phage display library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>5e8</Library_Complexity>
<Library_Titer>1e12</Library_Titer>
<Library_From>Mehdi Houimel</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Circular</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>138</Library_ID>
<Library_Name>X9 T7 phage display library</Library_Name>
<Library_Length>9</Library_Length>
<Library_Complexity>1e8</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Roberto Diaz</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>Random nonamer peptides are displayed on T7 phages as fusion proteins with the amino terminus of 10A capsid protein.</Comments>
</Item><Item><Library_ID>139</Library_ID>
<Library_Name>CX7-10C T7 phage display library</Library_Name>
<Library_Length>7-10</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Novagen</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Circular</Library_Topology>
<Comments>A mixture of 4 cyclic libraries CXnC was used which displayed 415 copies of the peptide on the capsid. Combined average diversity of the libraries was 1e8. The libraries were based on the T7Select 415-1b vector from Novagen.</Comments>
</Item><Item><Library_ID>140</Library_ID>
<Library_Name>X7 T7 phage display library</Library_Name>
<Library_Length>7</Library_Length>
<Library_Complexity>1e7</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Mark R. Spaller</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>The library was based on the T7 select 415-1 vector from Novagen. Eahg phage particle can displays 415 X7 peptides.</Comments>
</Item><Item><Library_ID>141</Library_ID>
<Library_Name>M13LP67-based X12 phage display library</Library_Name>
<Library_Length>12</Library_Length>
<Library_Complexity>2.1e8</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Yuzhang Wu</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>142</Library_ID>
<Library_Name>Ph.D.-12 and Ph.D.-C7C phage display library pool</Library_Name>
<Library_Length>7, 12</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>New England BioLabs, Beverly, MA, USA</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology></Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>143</Library_ID>
<Library_Name>f8-9mer phage display library (X9)</Library_Name>
<Library_Length>9</Library_Length>
<Library_Complexity>2.0e9</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>V. A. Petrenko</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item><Item><Library_ID>144</Library_ID>
<Library_Name>CX10C P99 β-lactamase-fusion library</Library_Name>
<Library_Length>10</Library_Length>
<Library_Complexity>6.1e7</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Girja S. Shukla</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Circular</Library_Topology>
<Comments>The library was constructed at the amino-terminus of the Enterobacter cloacae P99 cephalosporinase molecule (P99 β-lactamase) with NNK-scheme of randomization. The β-lactamase enzyme acted as a reporter, saving time and resources otherwise required by the phage-ELISA of a typical phage display screening.</Comments>
</Item><Item><Library_ID>145</Library_ID>
<Library_Name>X12 P99 β-lactamase-fusion library</Library_Name>
<Library_Length>12</Library_Length>
<Library_Complexity>4.9e7</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Girja S. Shukla</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>The library was constructed at the amino-terminus of the Enterobacter cloacae P99 cephalosporinase molecule (P99 β-lactamase) with NNK-scheme of randomization. The β-lactamase enzyme acted as a reporter, saving time and resources otherwise required by the phage-ELISA of a typical phage display screening.</Comments>
</Item><Item><Library_ID>146</Library_ID>
<Library_Name>Three pools of fUSE5 phage display library</Library_Name>
<Library_Length>7-12</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Chun-Mei Li</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology></Library_Topology>
<Comments>Random peptides were inserted to the minor capsid protein PIII of a filamentous bacteriophage fUSE5. Three pools of such libraries with peptides displayed on the surface of the phage particles were screened. Pool I was composed of four libraries of linear 7- to 11-aa peptides and pool II of three libraries of 9- to 12-aa peptides crosslinked via terminal cysteines, and pool III contained a mix of five libraries with both linear and crosslinked peptides, 8 to 10 aa long.</Comments>
</Item><Item><Library_ID>147</Library_ID>
<Library_Name>Min-23-R10 phage display library</Library_Name>
<Library_Length>10</Library_Length>
<Library_Complexity>2.8e8</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Christelle Souriau</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>The library was constructed by PCR using a set of degenerate primers to amplify Min-23 and replace residues 17-20 by 10 random residues ( LMRCKQDSDCLAGSVC(X)10FCG ).</Comments>
</Item><Item><Library_ID>148</Library_ID>
<Library_Name>YLK-(NNK)6 phage display library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>4.6e7</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Fujie Tanaka</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>The library was appended to the N-terminus of the peptide (YKLLKELLAKLKWLLRKLXXXXXX, X = any of the natural 20 amino acids).</Comments>
</Item><Item><Library_ID>149</Library_ID>
<Library_Name>(NNK)6-YLK Library</Library_Name>
<Library_Length>6</Library_Length>
<Library_Complexity>4.7e7</Library_Complexity>
<Library_Titer></Library_Titer>
<Library_From>Fujie Tanaka</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme>NNK</Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments>The library was appended to the C-terminus of the peptide (XXXXXXYKLLKELLAKLKWLLRKL, X = any of the natural 20 amino acids).</Comments>
</Item><Item><Library_ID>150</Library_ID>
<Library_Name>X12 T7 phage display library</Library_Name>
<Library_Length>12</Library_Length>
<Library_Complexity></Library_Complexity>
<Library_Titer>9e10</Library_Titer>
<Library_From>Novagen</Library_From>
<Library_Randomness>Completely random</Library_Randomness>
<Library_Scheme></Library_Scheme>
<Library_Topology>Linear</Library_Topology>
<Comments></Comments>
</Item></Library></result>