<result><BiopanningDataSet><Item><BiopanningDataSetID>2001</BiopanningDataSetID>
<Peptides>SVSVGRKPSPRP
NHRHYAMARNQS
SFKPSGLPAQSL
LSPHRSPQSPYS
QRLNDHENPGHT
HQMQSLSSNAST
NNSQKPAPVSPF
HSSLKLPNLSHR</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>8</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning>2</Rounds_of_Panning>
<Reference>PMID:22960048</Reference>
<Target_Name>Mouse gut</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>Animals underwent injection of the phage library in 200 ul of normal saline via tail vein at 4h following  30%  TBSA  burn  injury  and  were  compared  to  sham.  One hour  following  injection  of the  phage  library,  animals  were  placed under general  anesthesia  with  isoflurane  and  a  segment of  the  distal ileum  was  harvested.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2002</BiopanningDataSetID>
<Peptides>SGHQLLLNKMPN(2)
QQMHLMSYAPGP(1)
QRLNDHENPVHT(1)
NNHTKSQNITIS(1)
SGHQLLLNKMPK(1)
SHPWNAQRELSV(1)
SIPSVAQSRSAT(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>7</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:22960048</Reference>
<Target_Name>Mouse gut</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>Animals underwent injection of the phage library in 200 ul of normal saline via tail vein at 4h following  30%  TBSA  burn  injury  and  were  compared  to  sham.  One hour  following  injection  of the  phage  library,  animals  were  placed under general  anesthesia  with  isoflurane  and  a  segment of  the  distal ileum  was  harvested.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2003</BiopanningDataSetID>
<Peptides>AKGHAETFSFSG(1)
GDFNSGHHTTTR(1)
SFKPSGLPAQSL(1)
SGHQLLLNKMPN(1)
DQRPLLTAGNPL(1)
ILANDLTAPGPR(2)
ISRPAPISVDMK(1)
SDNVHTWQAMFK(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>8</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:22960048</Reference>
<Target_Name>Mouse gut</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>Animals underwent injection of the phage library in 200 ul of normal saline via tail vein at 4h following  30%  TBSA  burn  injury  and  were  compared  to  sham.  One hour  following  injection  of the  phage  library,  animals  were  placed under general  anesthesia  with  isoflurane  and  a  segment of  the  distal ileum  was  harvested.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2004</BiopanningDataSetID>
<Peptides>CSKAYLLLGQTC
CKRTKAQILLAPC
CTLRGKPYSLLGIC
SIRKALNILGYPDYD
CRKTTWILGEPLKC
CEQTKTDRLLGNAC
CEKASKILGVC</Peptides>
<Motif>K-A-x(2)-[IL]-L-G</Motif>
<Unique_Sequence_Number>7</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:11179221</Reference>
<Target_Name>G protein β1γ1 subunits</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>f88-4 phage display library pool</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description>The libraries were incubated with b-βγ subunites that had been bound to immobilized streptavidin on a microtiter plate.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2005</BiopanningDataSetID>
<Peptides>HPTTNTAHFFIT(1)
SPVEALLTHRLH(1)
NPIEQMLDYAKS(1)
DHYAPERRPFFQ(1)
SPVESRLHSNSS(1)
NMVERMIERPSR(1)
DHYAPERRPFFQ(1)
HPTTNTADFFIT(1)
NPVEMWSEMQHI(1)
DHYAPERRPFFQ(1)
TAHPTYKPPSPN(2)
YDNGFSNSHMPL(1)
QPLEHASHLTDV(1)
HIDGTSLTLKKT(1)
KAFAGTHTDTIT(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>15</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:22796092</Reference>
<Target_Name>Human immunoglobulin G (hIgG)</Target_Name>
<Template_Name>Immunoglobulin G-binding protein A</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>To screen the positive or specifically binding phages,phage solution were added to the hIgG-coated beads.Before proceeding to the next round of biopanning,non-specific phages that were included in the selected phages were removed by a 'subtraction' step by using magnetic particles without a hIgG coating.The supernatant from this subtraction step was introduced  to the next round.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2006</BiopanningDataSetID>
<Peptides>HSACDLPMHPMC(6)
HSACDLLMHPMC(1)
HSACDLPKAPWC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>3</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>6</Rounds_of_Panning>
<Reference>PMID:22821302</Reference>
<Target_Name>CD59</Target_Name>
<Template_Name>T-cell surface antigen CD2</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></Brief_Description>
<BiopanningDataSet_Comments>All of these three screened amino acid sequences had nine hydrophobic residues.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2007</BiopanningDataSetID>
<Peptides>LEYTWGNHPOSR
LEYTWRNHPOSR
FRYTWGNHPHRG
LRYTWGNWPLTA
HNLEYTWGNWPM
QHDSTYPWRNHP
DMWMNHESYSNN
PRLPFLHLTLEY
TSLDKYTELQDY
HDMRHRHMYOIA</Peptides>
<Motif>[LF]-[ER]-Y-T-W-[GR]-N-[HW]-P </Motif>
<Unique_Sequence_Number>10</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:22824180</Reference>
<Target_Name>Anti-Bla g 2 monoclonal antibody 7C11</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></Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2008</BiopanningDataSetID>
<Peptides>RIRALFGRSPVPCCV(2)
MRRPAPWLASRLMRP(1)
GRLRYTSHSARIQRV(2)
RSALRCLARVESCRQ(1)
ARHQRFLSSIQRAPF(1)
ALVRHPGARLRSFTA(1)
ARFRHSTKSAQFVPL(1)
GRLRPAKNHSVTVRR(1)
PRRHGFSPSVRAVLP(1)
RVPPRYHAKISPMVK(13)
RRPHSSHSHVSRFTS(1) </Peptides>
<Motif>R-x(2)-A-x-[FW]-x(2)-S-x-[VL]</Motif>
<Unique_Sequence_Number>11</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:23000297</Reference>
<Target_Name>Trisialogangliosides (GT1b)</Target_Name>
<Template_Name>Tetanus toxin</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 fUSE5 phage display library</Library_Name>
<Affinity_Measurement_Method></Affinity_Measurement_Method>
<Affinity_Measurement_Description></Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>The consensus motif(R-x(2)-A-x-[FW]-x(2)-S-x-[VL]) of the GT1b-binding peptides had one
cationic amino acid,one hydrophilic amino acid, and multiple
hydrophobic amino acids. Carbohydrate recognition in which
the amino acids in the motif were considered to be involved
was suggested by the combi-nation of hydrophobic interaction
and hydrogen bonds as well as glycan-binding proteins.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2009</BiopanningDataSetID>
<Peptides>GGHRPRFSGSFVASRA(1)
GVNRALPARWELWYPR(1)
GHGLNAHLRPRPFLAR(1)
GRNWNWPLRARVLSDA(1)
GGRFHARPRTSSVWSF(1)
GGTYYKRFGHSIPLVG(4)
GPRRHRFSPSVRAVLP(2)
GPRRGHFDESRFVHAV(1)
GSSFSSGFVNWHRFAA(1)
GYWPIDHKRVPLSRLV(1)
GASRSRFTSHWKRRTI(1)
GHRTQLNRLRSHRSVV(1)
GGGRFPHARDRVSFSR(2)</Peptides>
<Motif>G-x(3)-[RK]-x(2)-G-x(2)-[VI], N-x(3)-P-x-R-x(2)-[LV]</Motif>
<Unique_Sequence_Number>13</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:23000297</Reference>
<Target_Name>Ganglioside GM2</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 fUSE5 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>2010</BiopanningDataSetID>
<Peptides>DFRRLPGAFWQLRQP(4)
GWWYKGRARPVSAVA(15)
RWGALLRGGAAALFQ(1)</Peptides>
<Motif>W-x(4)-R-x(4)-[SA]</Motif>
<Unique_Sequence_Number>3</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:23000297</Reference>
<Target_Name>Ganglioside GD1a</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 fUSE5 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>2011</BiopanningDataSetID>
<Peptides>FAPQTTFTRPPY
FTTPTTFARPQY
SGHQPMLNKMPN
FRSFESCLAKSH
FTTPTTFARPPY
YGHQRMLNKLPY
FTTPNDFCSSSV
FTTSLFDRDFCS
GGYDLKRPLARP
APEKSLIRNVHD
SLSQHMLSSPSF
TSSLVTARSILS
LLPPDKSPRVFA
ESKLPLPGAPEP</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>14</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:23000375</Reference>
<Target_Name>Interleukin-10 receptor subunit alpha (IL-10RA)</Target_Name>
<Template_Name>Interleukin-10, IL-10</Template_Name>
<Structure_of_Target_Template_Complex>1J7V,1Y6K,</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></Brief_Description>
<BiopanningDataSet_Comments>Fourteen different peptides from low affinity to high affinity for functional characterization are selected. All the peptides were further ascertained for binding to shIL-10Ra by ELISA,of which peptide-04 (FRSFESCLAKSH) showed slowest dissociation.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2012</BiopanningDataSetID>
<Peptides>VPHNPGLISLQG(9)
DPHNGRFPSTQL(3)
VPKNLRFPSTSL(1)
QHGKPGSIPLQG(1)
LHVNPGLQTLQG(1)
VPTNVQLHVLQG(1)
VQHHPGIPDLQG(1)
ARLHMYSTDVQS(1)</Peptides>
<Motif>VPHNPGLISLQG</Motif>
<Unique_Sequence_Number>8</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>8</Rounds_of_Panning>
<Reference>PMID:23017232</Reference>
<Target_Name>Staphylococcus aureus, S.aureus</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>The phage library was twice depleted of clones binding to E.coli ATCC 700928 and S.epidermidis ATCC 35983,prior to affinity selection of clones binding to S.aureus to ensure  specificty.                                         </Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2013</BiopanningDataSetID>
<Peptides>HSACDLPMHPMC(6)[0.688 ± 0.033]
HSACDLLMHPMC(1)[0.659 ± 0.033]
HSACDLPKAPWC(1)[0.702 ± 0.035]</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>3</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>6</Rounds_of_Panning>
<Reference>PMID:22945508</Reference>
<Target_Name>CD59</Target_Name>
<Template_Name>T-cell surface antigen CD2</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>ELISA</Affinity_Measurement_Method>
<Affinity_Measurement_Description>In phage ELISA, the absorbance at 490 nm was determined. Data were reproduced from the graph and expressed as means ± SDs. The absorbances of phages with the same sequence were calculated as mean ± SD. The absorbance of the wild-type M13 phage was 0.121 ± 0.006.</Affinity_Measurement_Description>
<Brief_Description></Brief_Description>
<BiopanningDataSet_Comments>The affinities of the 13 phage clones to human CD59 were measured by ELISA.Eight clones showed a high binding to CD59.All sequences exhibited 9 hydrophobic residues.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2014</BiopanningDataSetID>
<Peptides>GPGTWRA
GPGTWRT
GPGTYRA
GHGTFRA
GEGTWRA
GPLTWRA
GPSTWRA
GPNTWRS
GPYTWRS</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>9</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:22869370</Reference>
<Target_Name>cAb29</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.-7 phage display library (X7)</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>2015</BiopanningDataSetID>
<Peptides>LLADTTHHRPWT
APLQPRSDNPFR
SATTPLIFPQTT
YPAPQPLVTKTS
ERSWTLDSALSM
QHSAAHYSTRLS
VDAQSKSYTLHD
SFHQLPARSPLP</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>8</Unique_Sequence_Number>
<Experimental_Method>Phage display (common panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:22941279</Reference>
<Target_Name>Boron nitride nanospheres,NNS</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></Brief_Description>
<BiopanningDataSet_Comments>Of these clones, LLADTTHHRPWT had the highest frequency .The BNNS-binding peptides were significantly rich in aromatic residues, including histidine (H) and tryptophan (W).</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2016</BiopanningDataSetID>
<Peptides>CHSNYNPRC
CHYHEQLRC
CKSMEADTC
CQKQPHSVC
CQKQDSTWC
CQTMLSLNC
CPAQLLNAC
CTVDKPPGC
CQPPFPRPC
CRFNTPLPC
CRHSANQTC
CYQDPRQPC
CEGLSEIEC
CPQLSDAGC
CLPLRSIQC
CLPNIDAKC
CPNSRVAAC
CRPSHATPC
CSAGFTWLC
CSLEHTWKC
CRSPHTTYC
CIESPTYWC
CHQSSPKLC
CQSSPPSLC
CLITPSRLC
CNPDRYYTC
CNSTHKMFC</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>27</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>1</Rounds_of_Panning>
<Reference>PMID:22661481</Reference>
<Target_Name>Mouse retina</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>RA retinas was used in the negative selection.The OIR retinas was used in positive selection.
                                                                                      
</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2017</BiopanningDataSetID>
<Peptides>CSTEALRHC(5)
CSHEALRHC(2)
CSSEAYRHC(1)
CNMDTARLC(1)
CSTTPSRMC(1)
CDSTTPRSC(1)
CSQPTLQAC(1)
CTPTTSPAC(1)
CMHSGPMAC(1)
CANLHHQQC(1)
CSEYLWSTC(1)
CNFTWTSLC(1)
CNKLEPFRC(1)
CYPTHPYSC(1)
CKWSPPQSC(1)
CMSPKNVSC(1)
CPTAKSASC(1)
CLAPTANSC(1)
CNQKTTSSC(1)
CVDKSFNIC(1)
CGLNVMRYC(1)
CPDNKLRQC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>22</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>2</Rounds_of_Panning>
<Reference>PMID:22661481</Reference>
<Target_Name>Mouse retina</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>RA retinas was used in the negative selection.The OIR retinas was used in positive selection.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2018</BiopanningDataSetID>
<Peptides>CSTEALRHC(15)
CDTTNSHLC(4)
CNQKTTSSC(2)
CNSYTNAAC(1)
CQQPTSGHC(1)
CTERQTRFC(1)
CRDMGNHIC(1)
CKTPFQHTC(1)
CGLNVMRYC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>9</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>3</Rounds_of_Panning>
<Reference>PMID:22661481</Reference>
<Target_Name>Mouse retina</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>RA retinas was used in the negative selection.The OIR retinas was used in positive selection.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2019</BiopanningDataSetID>
<Peptides>CSTEALRHC(15)
CLQMTKNSC(2)
CNQKTTSSC(1)
CTERQTRFC(1)
CANLHHQQC(1)
CSEYLWSTC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>6</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>4</Rounds_of_Panning>
<Reference>PMID:22661481</Reference>
<Target_Name>Mouse retina</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>RA retinas was used in the negative selection.The OIR retinas was used in positive selection.</Brief_Description>
<BiopanningDataSet_Comments></BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2020</BiopanningDataSetID>
<Peptides>CSTEALRHC(23)
CNQKTTSSC(1)
CTERQTRFC(1)
CSEYLWSTC(1)
CKTPFQHTC(1)</Peptides>
<Motif></Motif>
<Unique_Sequence_Number>5</Unique_Sequence_Number>
<Experimental_Method>Phage display (subtractive panning)</Experimental_Method>
<Rounds_of_Panning>5</Rounds_of_Panning>
<Reference>PMID:22661481</Reference>
<Target_Name>Mouse retina</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>RA retinas was used in the negative selection.The OIR retinas was used in positive selection.</Brief_Description>
<BiopanningDataSet_Comments>The phage harboring a peptide insert consisting of STEALRH distinguished between abnormal neovessels and normal vasculature.</BiopanningDataSet_Comments>
</Item><Item><BiopanningDataSetID>2021</BiopanningDataSetID>
<Peptides>CSGGGPGVC
CRLGGGLAC
CWWGGGVSC
CGSARGGGC
CARGGGIRC
CRAAGGGGC
CGSSAGGGC
CLGEAGGGC
CGGLEGGGC
CGNGGGESC
CSTGGGCSC
CLGGGEEWC </Peptides>
<Motif>G-G-G</Motif>
<Unique_Sequence_Number>12</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:11821895</Reference>
<Target_Name>Human bone</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>2022</BiopanningDataSetID>
<Peptides>CHGFSHHGC
CRRGFSLGC
CGGFSPWLC
CGRLVGFSC
CTTGVGFSC</Peptides>
<Motif>G-F-S</Motif>
<Unique_Sequence_Number>5</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:11821895</Reference>
<Target_Name>Human marrow</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>2023</BiopanningDataSetID>
<Peptides>CAEEGGTSC
CEGGSFNWC
CIEGGQVGC
CEGGSVESC
CEGGIFWHC
CEGGLSGCC
CCAEGGASC
CAEGGVRGC
CAEGGRVYC
CVVEGGVKC
CVLVGEGGC
CTKKLEGGC </Peptides>
<Motif>E-G-G</Motif>
<Unique_Sequence_Number>12</Unique_Sequence_Number>
<Experimental_Method>Phage display (in vivo)</Experimental_Method>
<Rounds_of_Panning></Rounds_of_Panning>
<Reference>PMID:11821895</Reference>
<Target_Name>Human fat</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>2024</BiopanningDataSetID>
<Peptides>CGGLSPNWC
CTGHLSPGC
CVLSPGLGC
CLSPGVKGC
CLSPWKKRC
CAWLSPARC
CAWRRLSPC
CLSPDDALC</Peptides>
<Motif>L-S-P</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 fat</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>2025</BiopanningDataSetID>
<Peptides>CLVSGGMAC
CLVSGCNTC
CDLVSGYGC
CLVSTSATC
CTALVSQTC
CWLVSGIGC
CLVSSVFPC
CPSLVSSVC
CGVSLVSTC
CQLVSGEPC
CNLVSRRLC
CLVSWRGSC
CDHFLVSPC
CGRGLVSLC
CFPVALVSC
CRWSSLVSC
CWSKSLVSC
CPGRSLVSC</Peptides>
<Motif>L-V-S</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 skeletal muscle</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></BiopanningDataSet></result>