<result><BiopanningDataSet><Item><BiopanningDataSetID>2026</BiopanningDataSetID>
<Peptides>CGRRAGGSC
CTRRAGGGC
CSRAGGLGC
CSYAGGLGC
CDVAGGLGC
CGAGGLGAC
CGAGGWGVC
CAGGTFKPC
CLGEVAGGC
CGSNDAGGC
CYRGIAGGC
CAGGVAGGC
CGGLAGGFC
CLLAGGVLC
CLVVSAGGC
CRTQAGGVC
CAGGFGEQC
CAGGLIDVC
CAGGSTWTC
CAGGDWWWC
CAGGGLLMC
CVAAGGGLC
CLYGAGGSC
CCALAGGCC
CIGAGGVHC</Peptides>
<Motif>A-G-G</Motif>
<Unique_Sequence_Number>25</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:11821895</Reference>
<Target_Name>Human prostate</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>A patient received an intravenous infusion of the unselected random phage library, and 15 min after infusion tissue biopsies were obtained to provide histopathological diagnosis and to recover phage from various organs. </Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2027</BiopanningDataSetID>
<Peptides>CGRRGSAGC(2)
CRPGRRGSC(1)
CSGRRGPRC(1)
CGLGRRNGC(1)
CGGRRSQTC(1)
CLWDGRRHC(1)
CGRRSVLTC(1)
CFGRRNLFC(1)
CGAGRRYWC(1)
CGRRLWATC(1)
CGVGRRFGC(1)
CLEMVGRRC(1)
CLSSIGRRC(1)
CGRRWIDVC(1)
CGRREEGLC(1)
CGRRVLGRC(1)
CRGLMGRRC(1)
CRFLLGRRC(1)
CPGVGRRLC(1)
CGVIDGRRC(1)
CADGRRLGC(1)
CAGRRAQIC(1)
CYGRRAREC(1)
CPGRRLRMC(1)
CGGRRVTLC(1)
CEQGGRRLC(1)
CSGRRLHPC(1)
CFDHSGRRC(1)
CGRRDVAIC(1)</Peptides>
<Motif>G-R-R</Motif>
<Unique_Sequence_Number>29</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:11821895</Reference>
<Target_Name>Human skin</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>A patient received an intravenous infusion of the unselected random phage library, and 15 min after infusion tissue biopsies were obtained to provide histopathological diagnosis and to recover phage from various organs. </Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2028</BiopanningDataSetID>
<Peptides>CGGHPRLAC
CGGHWRVNC
CGGHILEVC
CGGHRAQSC
CGDGGHRPC
CSCVGGHSC
CGSGVGGHC
CVRGWGGHC
CWRGWGGHC</Peptides>
<Motif>G-G-H</Motif>
<Unique_Sequence_Number>9</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:11821895</Reference>
<Target_Name>Human skin</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>A patient received an intravenous infusion of the unselected random phage library, and 15 min after infusion tissue biopsies were obtained to provide histopathological diagnosis and to recover phage from various organs.                                     </Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2029</BiopanningDataSetID>
<Peptides>CWGSKGTVC
CTGSLGTVC
CWGTVSDAC
CATGTVGPC
CVVGTVAWC
CWVVGTVTC
CRVVHGTVC
CGTVRFFSC</Peptides>
<Motif>G-T-V</Motif>
<Unique_Sequence_Number>8</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:11821895</Reference>
<Target_Name>Human skin</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>A patient received an intravenous infusion of the unselected random phage library, and 15 min after infusion tissue biopsies were obtained to provide histopathological diagnosis and to recover phage from various organs.                                     </Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2030</BiopanningDataSetID>
<Peptides>CPKHGVLWC
CSGVLWYHC
CGVLWAFGC
CQARGVLWC
CGVLVSRMC
CGTVGVLVC
CVGVLLPAC
CGGVLLLSC
CSGVLIHDC
CPYFGVLAC
CFFVSGVLC
CLLAGGVLC
CGEMGGVLC
CGRAYGVLC
CSGVLDG
CWWGGVLGC
CVWSRGVLC
CGVLRGVSC
CSFGVLRGC
CKGSVGVLC
CGGHFGVLC
CWMDVGVLC
CAFRVGVLC
CGVGVLRKC</Peptides>
<Motif>G-V-L</Motif>
<Unique_Sequence_Number>35</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:11821895</Reference>
<Target_Name>Human multiple organs</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>A patient received an intravenous infusion of the unselected random phage library, and 15 min after infusion tissue biopsies were obtained to provide histopathological diagnosis and to recover phage from various organs.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2031</BiopanningDataSetID>
<Peptides>CMEGRGAGC
CSEGRGFMC
CVEGRNSKC
CVEGRYTPC
CFNEGRQMC
CFEGRSRSC
CDHVVEGRC
CWDGTEGRC
CLDWREGRC
CRGCEGRVC
CMTPEGRVC
CRLFEGRVC
CREGRRMCC
CTQFEGRRC
CSMEGRMFC
CPGSAEGRC
CGEGRILAC
CEGRFSAWC
CEGRSDIWC
CEGRARWLC
CEGRERWRC</Peptides>
<Motif>E-G-R</Motif>
<Unique_Sequence_Number>21</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:11821895</Reference>
<Target_Name>Human multiple organs</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>A patient received an intravenous infusion of the unselected random phage library, and 15 min after infusion tissue biopsies were obtained to provide histopathological diagnosis and to recover phage from various organs. </Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2032</BiopanningDataSetID>
<Peptides>CCQCGFGVC(1)
CRGGFGVRC(1)
CAVGFGVIC(2)
CIVGFGVAC(1)
CGNFGVVWC(1)
CDEPFGVAC(1)
CVWFGVGSC(1)
CWFGVSLSC(1)
CFGVGQWAC(1)
CSMRFGVSC(1)
CRFGVWTGC(1)
CRFGVGRVC(1)
CSGLFGVYC(1)
CMKGVFGVC(1)
CAFGVVSDC(1)
CLYAFGVVC(1)
CKVFGVVEC(1)
CFGVRTDLC(1)
CTIFGVRRC(1)</Peptides>
<Motif>F-G-V</Motif>
<Unique_Sequence_Number>19</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:11821895</Reference>
<Target_Name>Human multiple organs</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>A patient received an intravenous infusion of the unselected random phage library, and 15 min after infusion tissue biopsies were obtained to provide histopathological diagnosis and to recover phage from various organs.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2033</BiopanningDataSetID>
<Peptides>CVWPRFGGC(1)
CSRFGGRVC(1)
CMKFGGRLC(1)
CRFGGALRC(1)
CERFGGDEC(1)
CFGGSVAPC(1)
CWFGGSVQC(1)
CFGGSWSLC(1)
CLLFGGSAC(1)
CMRLFGGTC(1)
CFGGFFMYC(2)
CEFGGQMNC(1)
CTFGGLILC(1)
CGNSFGGWC(1)
CRTFGGAGC(1)
CWVFGGKSC(1)
CRGFGGLSC(1)
CLWPSFGGC(1)</Peptides>
<Motif>F-G-G</Motif>
<Unique_Sequence_Number>18</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:11821895</Reference>
<Target_Name>Human multiple organs</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>A patient received an intravenous infusion of the unselected random phage library, and 15 min after infusion tissue biopsies were obtained to provide histopathological diagnosis and to recover phage from various organs.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2034</BiopanningDataSetID>
<Peptides>CGERISGPC
CGERLSSRC
CTEGERAGC
CWWLGERVC
CWAWAGERC
CGVISGERC
CGPGGERGC
CLGGGERDC
CDIAGERVC
CSRSKGERC
CKRKGERVC
CSRPGERQC
CCMRRGERC
CTLRGERNC
CFGERNRIC
CRGERWDLC
CGERTALLC</Peptides>
<Motif>G-E-R</Motif>
<Unique_Sequence_Number>17</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:11821895</Reference>
<Target_Name>Human multiple organs</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>A patient received an intravenous infusion of the unselected random phage library, and 15 min after infusion tissue biopsies were obtained to provide histopathological diagnosis and to recover phage from various organs.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2035</BiopanningDataSetID>
<Peptides>CPSGTSSWC
CSMSGTGMC
CLFDVSGTC
CVTGLSGTC
CNMVISGTC
CGVSGTLGC
CRSGTPGKC
CGRSGTSGC
CIYSGTLWC
CCSGTLFCC
CRSGTLQTC
CLGSGTWSC
CESGTATGC
CFTERSGTC
CRYLRSGTC
CPLGSSGTC</Peptides>
<Motif>S-G-T</Motif>
<Unique_Sequence_Number>16</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:11821895</Reference>
<Target_Name>Human multiple organs</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>A patient received an intravenous infusion of the unselected random phage library, and 15 min after infusion tissue biopsies were obtained to provide histopathological diagnosis and to recover phage from various organs.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2036</BiopanningDataSetID>
<Peptides>CTARSPWIC(12)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>1</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:22797828</Reference>
<Target_Name>Nd2O3 nanocrystals</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-C7C phage display library (CX7C)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>This phage displayed sequence TARSPWI flanked by two cysteines exhibited about 24,000 times greater affinity towards Nd2O3 nanocrystals than a random phage in the same-tube competitive binding assay. </BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2037</BiopanningDataSetID>
<Peptides>AYQRFDDVASRF(10)
VNLRMDDHDWSR(6)
KWNMNEDQIFFR(3)
AYKQTYHETTWF(3)
INLQTSTLMSHT(1)  
IHLDHGTVAPIW(1)  </Peptides>
<Motif>[ED]-D</Motif>
<Unique_Sequence_Number>6</Unique_Sequence_Number>
<Experimental_Method>Phage display (competitive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:22868630</Reference>
<Target_Name>Human mammary carcinoma cell line SK-BR-3</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>Ph.D.-12 phage display library (X12)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>After the first selection, the acid eluted buffer was changed with Herceptin?.
</Brief_Description>
<BiopanningDataSet_Comments>The shown sequences of peptides revealed that 40% peptides shared a consensus sequence (AYQRFDDVASRF).Consensus amino acid motifs (DD/ED) appeared at high frequencies.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2038</BiopanningDataSetID>
<Peptides>AEHYTFPKHSVWDIPYI
AEQTPKHSLWTPYTYPA
AEAHYKHSCRQDFCPTL</Peptides>
<Motif>K-H-S</Motif>
<Unique_Sequence_Number>3</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>DOI:10.1002/ddr.430330203</Reference>
<Target_Name>Human Platele</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>X15 M13 phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2039</BiopanningDataSetID>
<Peptides>AEKNIVTYIPRGDMPTM
AEYKHPRGDSPTHHQFG
AEARIMRGDMPSSNHFT</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>3</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>DOI:10.1002/ddr.430330203</Reference>
<Target_Name>Human Platele</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>X15 M13 phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2040</BiopanningDataSetID>
<Peptides>AEPGLAISCKRDVCITS</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>1</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>DOI:10.1002/ddr.430330203</Reference>
<Target_Name>Human Platele</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>X15 M13 phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2041</BiopanningDataSetID>
<Peptides>AETQYPHPVCRGDCNMW
AEPRGDWSTFRTHDTLF</Peptides>
<Motif>R-G-D</Motif>
<Unique_Sequence_Number>2</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>DOI:10.1002/ddr.430330203</Reference>
<Target_Name>Human Platele</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>X15 M13 phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>Peptides contained KGD sequences suggesting that these fusion peptides bound to the glycoprotein IIb-IIIa(GPIIb-llla).</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2042</BiopanningDataSetID>
<Peptides>AETLLDQGGHAVQLGDV</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>1</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>DOI:10.1002/ddr.430330203</Reference>
<Target_Name>Human Platele</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>X15 M13 phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>
</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2043</BiopanningDataSetID>
<Peptides>AEFSKKTSEAFPVWRLM
AEASVRSYLHKRLEHPL
AEFYRPSLLTAWYSNMP
AESASFSCRSDYCITST
AELFSTHYLAFKEDYSQ
AEEKHWLYVPDWTTAP
AEEKHWLYSPCLVHCP</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>7</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>DOI:10.1002/ddr.430330203</Reference>
<Target_Name>Human Platele</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>X15 M13 phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2044</BiopanningDataSetID>
<Peptides>YRHSVI
LRHSVI
WRHSVV
LRHSVV</Peptides>
<Motif>R-H-S-V </Motif>
<Unique_Sequence_Number>4</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:1376364</Reference>
<Target_Name>Anti-P53 monoclonal antibody PAb240</Target_Name>
<Template_Name>p53 protein </Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>f3-6mer phage display library (X6)</Library_Name>
<Affinity_Measurement_Method>ELISA</Affinity_Measurement_Method>
<Affinity_Measurement_Description>A wild-type phage control gave a background signal of 0.080. Phage clones giving a signal above 0.230 (~65%) were considered positive (data not shown). The average signal obtained from the positive clones was 0.452; the maximal signal 0.757.</Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>All four sharing a common RHSV tetrapeptide core sequence.The C-terminal residue of the encoded hexapeptide  as either valinr or isoleucine.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2045</BiopanningDataSetID>
<Peptides>ADGGAQGTA(21)
PGPSRAHFL(19)
LSSREPQAR(11)
RLTRELYAQ(9)
YTQKHKHQA(4)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>5</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:7504991</Reference>
<Target_Name>Sera from RA patients</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>pVIII-9aa phage display library (X9)</Library_Name>
<Affinity_Measurement_Method>ELISA,Competition experiment</Affinity_Measurement_Method>
<Affinity_Measurement_Description>The binding of the sera from RA patients and normal individual (both not included in the pool) to the phage displaying pepl (ADGGAQGTA) was investigated by ELISA. The percentage of the sera positive for pepl was significantly raised in RA (44%) compared to the controls (13%). Similar results were obtained with the other selected phages. Then the reactivity of the phage displaying pepl was investigated in detail. In competitive ELISA, the binding of the sera to phage-coated plates was significantly inhibited by the phage itself, whereas no inhibition was obtained with an unrelevant phage displaying a different peptide. In competitive inhibition a synthetic peptide corresponding to the peptide displayed by the phage (ADGGAQGTA), inhibited the binding of the sera to the phage by 56%.</Affinity_Measurement_Description>
<Brief_Description>Phages isolated during the second round of panning on RA sera were incubated with 100 pg of ammonium-precipitated immunoglobulins obtained from a pool of  40 normal individuals. After panning for 10 min on a plate coated with streptavidin, the non adherent phages (depletion step) were collected. RA sera was used in the positive selection. Ammonium-precipitated immunoglobulins from a pool of 40 normal individuals were used in the negtive selection. </Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2046</BiopanningDataSetID>
<Peptides>APWLYGPA</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>1</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:7685300</Reference>
<Target_Name>Anti-LeY antigen monoclonal antibody B3</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>X8 and CX8C phage display library pool</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Phage that bind to the biotinylated mAb B3 were enriched by several cycles of biopanning on streptavidin-coated petri dishes.</Brief_Description>
<BiopanningDataSet_Comments>Alanine-scanning mutagenesis of the sequence coding for this peptide indicates that four residues,PWLY,were critical for binding to the  mAb.  </BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2047</BiopanningDataSetID>
<Peptides>HGRFILPWWYAFSPS
RFRGLISLSQVYLSP
ARVSFWRYSSFAPTY</Peptides>
<Motif>W-Y-A-[WF]-S-P</Motif>
<Unique_Sequence_Number>3</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:9237904</Reference>
<Target_Name>Thomsen-Friedenreich antigen (T antigen, TF antigen)</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>f3-15mer phage display library (X15)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Wells of the microtiter plates were first coated with streptavidin, washed with TPBS (phosphate buffered saline, pH 7.4, 0.5% (v/v) Tween-20), and blocked with 3% (w/v) BSA prior to addition of biotinylated antigens. Phages were incubated with antigen prior to washing and elution. In the last two rounds of some procedures, phages were pre-incubated with the biotinylated antigens before the streptavidin capture.</Brief_Description>
<BiopanningDataSet_Comments>A putative consensus sequence of W-Y-A-[WF]-S-P was present in the most frequently occurring clone, P30(HGRFILPWWYAFSPS).</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2048</BiopanningDataSetID>
<Peptides>GSWYAWSPLVPSAQI</Peptides>
<Motif>W-Y-A-[WF]-S-P</Motif>
<Unique_Sequence_Number>1</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:9237904</Reference>
<Target_Name>Thomsen-Friedenreich antigen (T antigen, TF antigen)</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>f88-15mer phage display library (X15)</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Wells of the microtiter plates were first coated with streptavidin, washed with TPBS (phosphate buffered saline, pH 7.4, 0.5% (v/v) Tween-20), and blocked with 3% (w/v) BSA prior to addition of biotinylated antigens. Phages were incubated with antigen prior to washing and elution. In the last two rounds of some procedures, phages were pre-incubated with the biotinylated antigens before the streptavidin capture.</Brief_Description>
<BiopanningDataSet_Comments>A putative consensus sequence of W-Y-A-[WF]-S-P was present in the most frequently occurring clone, P10(GSWYAWSPLVPSAQI).</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2049</BiopanningDataSetID>
<Peptides>CGFECVRQCPERC</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>1</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:9664085</Reference>
<Target_Name>Mouse lung</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>CX3CX3CX3C phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Mice were first anesthetized with Avertin and then injected intravenously (tail vein) with phage peptide library.Organs were then weighed, homogenized, and the phage were rescued by infection with K91kan bacteria. </Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2050</BiopanningDataSetID>
<Peptides>CGFELETC
CTLRDRNC
CIGEVEVC</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>3</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:9664085</Reference>
<Target_Name>Mouse lung</Target_Name>
<Template_Name>Not determined.</Template_Name>
<Structure_of_Target_Template_Complex>Not determined.</Structure_of_Target_Template_Complex>
<Structure_of_Target_Peptide_Complex>Not determined.</Structure_of_Target_Peptide_Complex>
<Library_Name>fdMED1-based CX6C M13 phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>Mice were first anesthetized with Avertin and then injected intravenously (tail vein) with phage peptide library.Organs were then weighed, homogenized, and the phage were rescued by infection with K91kan bacteria. </Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item></BiopanningDataSet></result>