Modification : 5'-Biotinylated and 5'-FAM Labeled

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AptBacDB_ID ⇅ PMID/DOI ⇅ Year ⇅ Title ⇅ Aptamer name ⇅ Sequence (5′ to 3′) ⇅ Length ⇅ Library ⇅ Type ⇅ Target Organism ⇅ Target ⇅ Objective/Mechanism ⇅ Outcome/Inhibitory effect ⇅ No. of selection round SELEX ⇅ Determination of affinity method ⇅ Kd value ⇅ Activity Role ⇅ Method ⇅ Modification ⇅ Cytotoxicity (cell viability) ⇅ Stability⇅ Potential Candidate ⇅ Half-life ⇅ Patent ⇅
ABdb_0757 271794222016Inhibition of the superantigenic activities of Staphylococcal enterotoxin A by an aptamer antagonistS6ATACCAGCTTATTCAATT-GCCGCGGAATTGTGGCTTGGTGTCGTGGTCAGGGGCTGG-AGATAGTAAGTGCAATCT755'-ATACCAGCTTATTCAATT-N40-AGATAGTAAGTGCAATCT-3'ssDNAStaphylococcus aureus (S. aureus)Staphylococcal Enterotoxin A (SEA)Identify aptamers that bind to and block superantigen activity of SEA.N/A9Enzyme-Linked Aptamer Assay (ELAA)N/ATherapeutics/ImmunmodulatorySELEX5'-Biotinylated and 5'-FAM LabeledN/AN/ABest CandidateN/AN/A
ABdb_0758 271794222016Inhibition of the superantigenic activities of Staphylococcal enterotoxin A by an aptamer antagonistS12ATACCAGCTTATTCAATT-GCCACTGTGGACTTGTTATTCGTCTTTGCCGTCTAATTCG-AGATAGTAAGTGCAATCT765'-ATACCAGCTTATTCAATT-N40-AGATAGTAAGTGCAATCT-3'ssDNAStaphylococcus aureus (S. aureus)Staphylococcal Enterotoxin A (SEA)Identify aptamers that bind to and block superantigen activity of SEA.Inhibited PBMCs proliferation with an inhibition rate of 84%.9Enzyme-Linked Aptamer Assay (ELAA)79.35 ± 12.09 nMTherapeutics/ImmunmodulatorySELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_0759 271794222016Inhibition of the superantigenic activities of Staphylococcal enterotoxin A by an aptamer antagonistS23ATACCAGCTTATTCAATT-GCAACAATGTTGTGTCAGCAAGTTGGTTGGCGGTGTATTG-AGATAGTAAGTGCAATCT765'-ATACCAGCTTATTCAATT-N40-AGATAGTAAGTGCAATCT-3'ssDNAStaphylococcus aureus (S. aureus)Staphylococcal Enterotoxin A (SEA)Identify aptamers that bind to and block superantigen activity of SEA.N/A9Enzyme-Linked Aptamer Assay (ELAA)N/ATherapeutics/ImmunmodulatorySELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1003 302059662018Generation and application of DNA aptamers against HspX for accurate diagnosis of tuberculous meningitisH63GTCTTGACTAGTTACGCC-GGGAACAATATGTTCAAGGGCTCTTTAAAGTTTTAGTTCGTTTG-TCATTCAGTTGGCGCCTC805'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (M.Tb.)HspX antigenIdentify an aptamer that binds to HspX and develop an assay to diagnose TBM in CSF samples.LOD was 32 ng for H63.8Isothermal Titration Calorimetry (ITC)3.71 x 10-7 ± 2.12 x 10-11 MDiagnosticSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/ABest CandidateN/AIndian Patent application no. 201611001550
ABdb_1004 302059662018Generation and application of DNA aptamers against HspX for accurate diagnosis of tuberculous meningitisH63 SL-2 M6AGGGCTTTTTTTTTTTTTAGTTCGTTTG285'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (M.Tb.)HspX antigenIdentify an aptamer that binds to HspX and develop an assay to diagnose TBM in CSF samples.Exhibited 2.5-fold higher binding with respect to the parent H63, and H63 SL-2 M6 has an LOD of 16 ng.8Isothermal Titration Calorimetry (ITC)9 x 10-8 ± 2 x 10-14 MDiagnosticSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/ABest CandidateN/AIndian Patent application no. 201611001550
ABdb_1005 302059662018Generation and application of DNA aptamers against HspX for accurate diagnosis of tuberculous meningitisH33GTCTTGACTAGTTACGCC-ACACTAGAAGGTATTTACTATTCTGTGTTAACATGTACTAGCCA-TCATTCAGTTGGCGCCTC805'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (M.Tb.)HspX antigenIdentify an aptamer that binds to HspX and develop an assay to diagnose TBM in CSF samples.N/A8Isothermal Titration Calorimetry (ITC)N/ADiagnosticSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AIndian Patent application no. 201611001550
ABdb_1006 302059662018Generation and application of DNA aptamers against HspX for accurate diagnosis of tuberculous meningitisH66GTCTTGACTAGTTACGCC-AAGTTTTAATACAACTCACATTAGGGAAAGCTTGCATCCAGGCC-TCATTCAGTTGGCGCCTC805'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (M.Tb.)HspX antigenIdentify an aptamer that binds to HspX and develop an assay to diagnose TBM in CSF samples.N/A8Isothermal Titration Calorimetry (ITC)N/ADiagnosticSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AIndian Patent application no. 201611001550
ABdb_1007 302059662018Generation and application of DNA aptamers against HspX for accurate diagnosis of tuberculous meningitisH70GTCTTGACTAGTTACGCC-CAGGACAGGTTAAAATTTTTCTGGATCCCTTTTCATTCTCCATGG-TCATTCAGTTGGCGCCTC815'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (M.Tb.)HspX antigenIdentify an aptamer that binds to HspX and develop an assay to diagnose TBM in CSF samples.N/A8Isothermal Titration Calorimetry (ITC)N/ADiagnosticSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AIndian Patent application no. 201611001550
ABdb_1008 302059662018Generation and application of DNA aptamers against HspX for accurate diagnosis of tuberculous meningitisH3GTCTTGACTAGTTACGCC-CATACACGGTTACACGTACTGGATAATGTTGATTATGCTTCTGC-TCATTCAGTTGGCGCCTC805'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (M.Tb.)HspX antigenIdentify an aptamer that binds to HspX and develop an assay to diagnose TBM in CSF samples.N/A8Isothermal Titration Calorimetry (ITC)N/ADiagnosticSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AIndian Patent application no. 201611001550
ABdb_1009 302059662018Generation and application of DNA aptamers against HspX for accurate diagnosis of tuberculous meningitisH18GTCTTGACTAGTTACGCC-TAGAACCAAACCTTGTGTAGAAGGGCTTCTCCCGTGTGCTTTGA-TCATTCAGTTGGCGCCTC805'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (M.Tb.)HspX antigenIdentify an aptamer that binds to HspX and develop an assay to diagnose TBM in CSF samples.N/A8Isothermal Titration Calorimetry (ITC)N/ADiagnosticSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AIndian Patent application no. 201611001550
ABdb_1010 302059662018Generation and application of DNA aptamers against HspX for accurate diagnosis of tuberculous meningitisH47GTCTTGACTAGTTACGCC-GGATGAACTGTTCCGCTGTGTATCACGCCAAAAGTCCTTATTTG-TCATTCAGTTGGCGCCTC805'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (M.Tb.)HspX antigenIdentify an aptamer that binds to HspX and develop an assay to diagnose TBM in CSF samples.N/A8Isothermal Titration Calorimetry (ITC)N/ADiagnosticSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AIndian Patent application no. 201611001550
ABdb_1011 302059662018Generation and application of DNA aptamers against HspX for accurate diagnosis of tuberculous meningitisH48GTCTTGACTAGTTACGCC-CATGAAACCATCTGGTCCGCAATGGGCGCTTGGAATATTCGTCA-TCATTCAGTTGGCGCCTC805'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (M.Tb.)HspX antigenIdentify an aptamer that binds to HspX and develop an assay to diagnose TBM in CSF samples.N/A8Isothermal Titration Calorimetry (ITC)N/ADiagnosticSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AIndian Patent application no. 201611001550
ABdb_1085 302454722018G-Quadruplex-Forming DNA Aptamers Inhibit the DNA-Binding Function of HupB and Mycobacterium tuberculosis Entry into Host CellsHupB-1GTCTTGACTAGTTACGCC-TAGGAAGGGAAGGAAGATAGAGAGTAGGTCGTCGGAGGCAGGGG-TCATTCAGTTGGCGCCTC805'-GTCTTGACTAGTTACGCC-N3-41X-TCATTCAGTTGGCGCCTC-3' (*N = 3nt sequence tag and **X = 41nt random region)ssDNAMycobacterium Tuberculosis (M.Tb.)Histone-like protein HupB (Rv2986c)Identify aptamers that recognise and inhibit the DNA-binding activity of HupB, and significantly block Mtb entry into THP-1 monocytic cells.Displayed the highest binding to HupB (≥5 fold relative to RDL).8Isothermal Titration Calorimetry (ITC)N/ATherapeuticsSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/APatent application no. 20171100124
ABdb_1086 302454722018G-Quadruplex-Forming DNA Aptamers Inhibit the DNA-Binding Function of HupB and Mycobacterium tuberculosis Entry into Host CellsHupB-2GTCTTGACTAGTTACGCC-TAGTAAAGGGGGTAAGAATCAATTGCGAGGTGGAGTGGGAGTGG-TCATTCAGTTGGCGCCTC805'-GTCTTGACTAGTTACGCC-N3-41X-TCATTCAGTTGGCGCCTC-3' (*N = 3nt sequence tag and **X = 41nt random region)ssDNAMycobacterium Tuberculosis (M.Tb.)Histone-like protein HupB (Rv2986c)Identify aptamers that recognise and inhibit the DNA-binding activity of HupB, and significantly block Mtb entry into THP-1 monocytic cells.Displayed the highest binding to HupB (≥5 fold relative to RDL).8Isothermal Titration Calorimetry (ITC)N/ATherapeuticsSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/APatent application no. 20171100124
ABdb_1087 302454722018G-Quadruplex-Forming DNA Aptamers Inhibit the DNA-Binding Function of HupB and Mycobacterium tuberculosis Entry into Host CellsHupB-4GTCTTGACTAGTTACGCC-TAGGTGATTGCTGGAGTGGGTAGCAGATGGGGGGGGGGTTCTTGG-TCATTCAGTTGGCGCCTC815'-GTCTTGACTAGTTACGCC-N3-41X-TCATTCAGTTGGCGCCTC-3' (*N = 3nt sequence tag and **X = 41nt random region)ssDNAMycobacterium Tuberculosis (M.Tb.)Histone-like protein HupB (Rv2986c)Identify aptamers that recognise and inhibit the DNA-binding activity of HupB, and significantly block Mtb entry into THP-1 monocytic cells.Displayed the highest binding to HupB (≥5 fold relative to RDL).8Isothermal Titration Calorimetry (ITC)N/ATherapeuticsSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/APatent application no. 20171100124
ABdb_1088 302454722018G-Quadruplex-Forming DNA Aptamers Inhibit the DNA-Binding Function of HupB and Mycobacterium tuberculosis Entry into Host CellsHupB-13GTCTTGACTAGTTACGCC-TTTGGGAAGGGGGGGGAGGAAGTTCGATGGTGTTGTGGACCGGG-TCATTCAGTTGGCGCCTC805'-GTCTTGACTAGTTACGCC-N3-41X-TCATTCAGTTGGCGCCTC-3' (*N = 3nt sequence tag and **X = 41nt random region)ssDNAMycobacterium Tuberculosis (M.Tb.)Histone-like protein HupB (Rv2986c)Identify aptamers that recognise and inhibit the DNA-binding activity of HupB, and significantly block Mtb entry into THP-1 monocytic cells.Displayed the highest binding to HupB (≥5 fold relative to RDL).8Isothermal Titration Calorimetry (ITC)N/ATherapeuticsSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/APatent application no. 20171100124
ABdb_1089 302454722018G-Quadruplex-Forming DNA Aptamers Inhibit the DNA-Binding Function of HupB and Mycobacterium tuberculosis Entry into Host CellsHupB-1TTAGGAAGGGAAGGAAGATAGAGAGTAGGTCGTCGGAGGCAGGGG445'-GTCTTGACTAGTTACGCC-N3-41X-TCATTCAGTTGGCGCCTC-3' (*N = 3nt sequence tag and **X = 41nt random region)ssDNAMycobacterium Tuberculosis (M.Tb.)Histone-like protein HupB (Rv2986c)Identify aptamers that recognise and inhibit the DNA-binding activity of HupB, and significantly block Mtb entry into THP-1 monocytic cells.N/A8Isothermal Titration Calorimetry (ITC)N/ATherapeuticsSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/APatent application no. 20171100124
ABdb_1090 302454722018G-Quadruplex-Forming DNA Aptamers Inhibit the DNA-Binding Function of HupB and Mycobacterium tuberculosis Entry into Host CellsHupB-2TTAGTAAAGGGGGTAAGAATCAATTGCGAGGTGGAGTGGGAGTGG445'-GTCTTGACTAGTTACGCC-N3-41X-TCATTCAGTTGGCGCCTC-3' (*N = 3nt sequence tag and **X = 41nt random region)ssDNAMycobacterium Tuberculosis (M.Tb.)Histone-like protein HupB (Rv2986c)Identify aptamers that recognise and inhibit the DNA-binding activity of HupB, and significantly block Mtb entry into THP-1 monocytic cells.N/A8Isothermal Titration Calorimetry (ITC)N/ATherapeuticsSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/APatent application no. 20171100124
ABdb_1091 302454722018G-Quadruplex-Forming DNA Aptamers Inhibit the DNA-Binding Function of HupB and Mycobacterium tuberculosis Entry into Host CellsHupB-4TTAGGTGATTGCTGGAGTGGGTAGCAGATGGGGGGGGGGTTCTTGG455'-GTCTTGACTAGTTACGCC-N3-41X-TCATTCAGTTGGCGCCTC-3' (*N = 3nt sequence tag and **X = 41nt random region)ssDNAMycobacterium Tuberculosis (M.Tb.)Histone-like protein HupB (Rv2986c)Identify aptamers that recognise and inhibit the DNA-binding activity of HupB, and significantly block Mtb entry into THP-1 monocytic cells.HupB-4T treated bacteria yielded reduced intracellular CFU by ∼57.8%.8Isothermal Titration Calorimetry (ITC)1.72 ± 0.00002 μM,TherapeuticsSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledNo loss in the viability of THP-1 cells was observed on exposure to aptamers.In fetal bovine serum (FBS) for 3 hr at 37°C, no change was observed in the integrity of aptamer bands.Best CandidateN/APatent application no. 20171100124
ABdb_1092 302454722018G-Quadruplex-Forming DNA Aptamers Inhibit the DNA-Binding Function of HupB and Mycobacterium tuberculosis Entry into Host CellsHupB-13TTTTGGGAAGGGGGGGGAGGAAGTTCGATGGTGTTGTGGACCGGG445'-GTCTTGACTAGTTACGCC-N3-41X-TCATTCAGTTGGCGCCTC-3' (*N = 3nt sequence tag and **X = 41nt random region)ssDNAMycobacterium Tuberculosis (M.Tb.)Histone-like protein HupB (Rv2986c)Identify aptamers that recognise and inhibit the DNA-binding activity of HupB, and significantly block Mtb entry into THP-1 monocytic cells.HupB-13T treated bacteria yielded reduced intracellular CFU by ∼45.5%.8Isothermal Titration Calorimetry (ITC)0.17 ± 0.00000005 μMTherapeuticsSubtractive SELEX5'-Biotinylated and 5'-FAM LabeledNo loss in the viability of THP-1 cells was observed on exposure to aptamers.In fetal bovine serum (FBS) for 3 hr at 37°C, no change was observed in the integrity of aptamer bands.Best CandidateN/APatent application no. 20171100124
ABdb_1214 317045872019Theranostic Application of a Novel G-Quadruplex-Forming DNA Aptamer Targeting Malate Synthase of Mycobacterium tuberculosisMS10-TruncGGTGGTGGTGG115'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (H37Rv)Surface-associated Malate synthase (MS -Whole cells)Identify aptamers that bind to and inhibit the MS enzyme activity, thereby blocking bacterial entry into host cells.Inhibited MS activity with an IC₅₀ of 251.1 nM; Ki of 230 nM; inhibited M. tb invasion into human THP-1 monocytic cells.10Surface Plasmon Resonance (SPR)1.9 × 10−11 MTherapeuticsSELEX5'-Biotinylated and 5'-FAM LabeledN/AN/ABest CandidateN/AIndian Patent application no. 201611021901
ABdb_1215 317045872019Theranostic Application of a Novel G-Quadruplex-Forming DNA Aptamer Targeting Malate Synthase of Mycobacterium tuberculosisMS4GGACCAGGTGAGTGGATGCGGGTGCGGGTGGGGGTGAGGGGGGG445'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (H37Rv)Surface-associated Malate synthase (MS -Whole cells)Identify aptamers that bind to and inhibit the MS enzyme activity, thereby blocking bacterial entry into host cells.Inhibition of MS activity, the aptamers were ranked as MS10 (IC50 of 275.6 nM, Ki of 270 nM) > MS5 > MS20 > MS4 > MS6.10Surface Plasmon Resonance (SPR)9.9 × 10−9 MTherapeuticsSELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1216 317045872019Theranostic Application of a Novel G-Quadruplex-Forming DNA Aptamer Targeting Malate Synthase of Mycobacterium tuberculosisMS5GCAGAGAGAGAGAAAGTGAGAAGGGCGGGGGGGAGAGGGTGGGG445'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (H37Rv)Surface-associated Malate synthase (MS -Whole cells)Identify aptamers that bind to and inhibit the MS enzyme activity, thereby blocking bacterial entry into host cells.Inhibition of MS activity, the aptamers were ranked as MS10 (IC50 of 275.6 nM, Ki of 270 nM) > MS5 > MS20 > MS4 > MS6.10Surface Plasmon Resonance (SPR)2.7 × 10−6 MTherapeuticsSELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1217 317045872019Theranostic Application of a Novel G-Quadruplex-Forming DNA Aptamer Targeting Malate Synthase of Mycobacterium tuberculosisMS6GGTGGGATGGGGGGGGGAGGGTAGGGTGTGCAAGTAGAGGGTC435'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (H37Rv)Surface-associated Malate synthase (MS -Whole cells)Identify aptamers that bind to and inhibit the MS enzyme activity, thereby blocking bacterial entry into host cells.Inhibition of MS activity, the aptamers were ranked as MS10 (IC50 of 275.6 nM, Ki of 270 nM) > MS5 > MS20 > MS4 > MS6.10Surface Plasmon Resonance (SPR)2.8 × 10−10 MTherapeuticsSELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1218 317045872019Theranostic Application of a Novel G-Quadruplex-Forming DNA Aptamer Targeting Malate Synthase of Mycobacterium tuberculosisMS10GGTGTGTTGACTGAGGGGGTGGGGTGGGTGGTGGTGGATATAGC445'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (H37Rv)Surface-associated Malate synthase (MS -Whole cells)Identify aptamers that bind to and inhibit the MS enzyme activity, thereby blocking bacterial entry into host cells.Inhibition of MS activity, the aptamers were ranked as MS10 (IC50 of 275.6 nM, Ki of 270 nM) > MS5 > MS20 > MS4 > MS6.10Surface Plasmon Resonance (SPR)1.2 × 10−8 MTherapeuticsSELEX5'-Biotinylated and 5'-FAM LabeledN/AN/ABest CandidateN/AN/A
ABdb_1219 317045872019Theranostic Application of a Novel G-Quadruplex-Forming DNA Aptamer Targeting Malate Synthase of Mycobacterium tuberculosisMS20GGGTTGTAAGAGGGAGCTGGGAGGGGTCGGGGGGGGGGGTGGC435'-GTCTTGACTAGTTACGCC-N44-TCATTCAGTTGGCGCCTC-3'ssDNAMycobacterium Tuberculosis (H37Rv)Surface-associated Malate synthase (MS -Whole cells)Identify aptamers that bind to and inhibit the MS enzyme activity, thereby blocking bacterial entry into host cells.Inhibition of MS activity, the aptamers were ranked as MS10 (IC50 of 275.6 nM, Ki of 270 nM) > MS5 > MS20 > MS4 > MS6.10Surface Plasmon Resonance (SPR)9.1 × 10−7 MTherapeuticsSELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1285 308595982019Selection and characterization of ssDNA aptamers specifically recognizing pathogenic Vibrio alginolyticusVA2GACGCTTACTCAGGTGTGACTCG-TCGGTCGGGTGGTTGGGGCGGGTGGTCGGTTTTTAAGTTGTGTCATTGTC-CGAAGGACGCAGATGAAGTCTC955'-GACGCTTACTCAGGTGTGACTCG-50N-CGAAGGACGCAGATGAAGTCTC-3'ssDNAVibrio AlginolyticusWhole cellIdentify aptamers targeted against viable V. alginolyticus.VA2 could recognize different V. alginolyticus prevalent in Beibu Gulf with high specificity and affinity.9Flow Cytometry14.31 ± 4.26 nMDetectionWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledNo cytotoxic effects shown in vitro and in vivo.N/ABest CandidateN/AN/A
ABdb_1291 308595982019Selection and characterization of ssDNA aptamers specifically recognizing pathogenic Vibrio alginolyticusVA8GACGCTTACTCAGGTGTGACTCG-CGTTTTATTGGTGTGGGGCTGGGGTGGTGGGTGGCTCTACTGGTTCCGTT-CGAAGGACGCAGATGAAGTCTC955'-GACGCTTACTCAGGTGTGACTCG-50N-CGAAGGACGCAGATGAAGTCTC-3'ssDNAVibrio AlginolyticusWhole cellIdentify aptamers targeted against viable V. alginolyticus.VA8 could recognize different V. alginolyticus prevalent in Beibu Gulf with high specificity and affinity but less potent than VA2.9Flow Cytometry90.00 ± 13.51 nMDetectionWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledNo cytotoxic effects shown in vitro and in vivo.N/ABest CandidateN/AN/A
ABdb_1341 https://doi.org/10.1016/j.snb.2018.12.1122019Screening of highly-specific aptamers and their applications in paper-based microfluidic chips for rapid diagnosis of multiple bacteriaA1ACAGCACCACAGACCACATATCACATGCTGTCGCCTTGCGATATCAATTCCAGTGATGTTTGTCTTCCTGCC725'-GGCAGGAAGACAAACA-N40-TGGTCTGTGGTGCTGT-3'ssDNAAcinetobacter BaumanniiWhole cellIdentify aptamers and develop a dual-aptamer, NC-based microfluidic chip for fast diagnosis of three common nosocomial bacteria.LOD was estimated to be 10(3) for AB.3Fluorescence Spectroscopy6.8 ± 1.9 nMDetectionWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1342 https://doi.org/10.1016/j.snb.2018.12.1122019Screening of highly-specific aptamers and their applications in paper-based microfluidic chips for rapid diagnosis of multiple bacteriaE27ACAGCACCACAGACCACAGATCATACCAGTGCGGCCGTTAGCCTCGTTAATCTGGCGTTTGTCTTCCTGCC715'-GGCAGGAAGACAAACA-N40-TGGTCTGTGGTGCTGT-3'ssDNAEscherichia Coli (E. Coli)Whole cellIdentify aptamers and develop a dual-aptamer, NC-based microfluidic chip for fast diagnosis of three common nosocomial bacteria.LOD was estimated to be 10(4) for EC.3Fluorescence Spectroscopy11.9 ± 3.7 nMDetectionWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1343 https://doi.org/10.1016/j.snb.2018.12.1122019Screening of highly-specific aptamers and their applications in paper-based microfluidic chips for rapid diagnosis of multiple bacteriaO28GGGGAAGACAAACACCTCATAGTCGGTATCGGCCGTTTGGGCGTTTTTCCGATGGTCTGTGGTGCTGT685'-GGCAGGAAGACAAACA-N40-TGGTCTGTGGTGCTGT-3'ssDNAMethicillin-resistant Staphylococcus aureus (MRSA)Whole cellIdentify aptamers and develop a dual-aptamer, NC-based microfluidic chip for fast diagnosis of three common nosocomial bacteria.LOD was estimated to be 10(5) CFU/μL for MRSA.3Fluorescence Spectroscopy199.6 ± 35.8 nMDetectionWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1462 326630062020Selection of Specific DNA Aptamers for Hetero-Sandwich-Based Colorimetric Determination of Campylobacter jejuni in FoodCJA1CTGCGATCAAGTTACGCACCTCGCCATGTTCCCCGCCCGGCATGTGTTATGCCCCTGTG595'-AGCAGCACAGAGGTCAGATG-N59-TTCACGGTAGCACGCATAGG-3'ssDNACampylobacter JejuniWhole cellIdentify aptamers and develop a hetero-sandwich-based assay for colorimetric analysis of C. jejuni from contaminated samples.C. jejuni can be detected from 1.7 × 10(1) to 1.7 × 10(6) CFU/mL. The limit of detection (LOD) is obtained as 10 CFU/mL in PBS and 13 CFU/mL in contaminated milk samples.12Fluorescence Binding Assay1.37 ± 0.28 nMDetectionWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/ABest CandidateN/AN/A
ABdb_1463 326630062020Selection of Specific DNA Aptamers for Hetero-Sandwich-Based Colorimetric Determination of Campylobacter jejuni in FoodCJA2GTTGGGTGCGGCGGGAGGGTCCCATCGGAAACCAAGCTGTGCTGAGATTTTTCCGCGAT595'-AGCAGCACAGAGGTCAGATG-N59-TTCACGGTAGCACGCATAGG-3'ssDNACampylobacter JejuniWhole cellIdentify aptamers and develop a hetero-sandwich-based assay for colorimetric analysis of C. jejuni from contaminated samples.N/A12Fluorescence Binding Assay1.78 ± 0.88 nMDetectionWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1464 326630062020Selection of Specific DNA Aptamers for Hetero-Sandwich-Based Colorimetric Determination of Campylobacter jejuni in FoodCJA3CACGCAAGTTAATCAGCGTGACATCAGGTCTAGATTCCGGCTTATAGCGCCAGGTTTCC595'-AGCAGCACAGAGGTCAGATG-N59-TTCACGGTAGCACGCATAGG-3'ssDNACampylobacter JejuniWhole cellIdentify aptamers and develop a hetero-sandwich-based assay for colorimetric analysis of C. jejuni from contaminated samples.N/A12Fluorescence Binding Assay2.01 ± 0.90 nMDetectionWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1465 326630062020Selection of Specific DNA Aptamers for Hetero-Sandwich-Based Colorimetric Determination of Campylobacter jejuni in FoodCJA4GGTGGGCTCTGTTCGGGAGGGGTATTGTTAGGACCGAGAGGCTGCATTCCGCCAGCTGC595'-AGCAGCACAGAGGTCAGATG-N59-TTCACGGTAGCACGCATAGG-3'ssDNACampylobacter JejuniWhole cellIdentify aptamers and develop a hetero-sandwich-based assay for colorimetric analysis of C. jejuni from contaminated samples.N/A12Fluorescence Binding Assay2.26 ± 0.91 nMDetectionWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1466 326630062020Selection of Specific DNA Aptamers for Hetero-Sandwich-Based Colorimetric Determination of Campylobacter jejuni in FoodCJA5GCTCTGTCTTTTCAGCTTTATCCGGGTGTGGTGGGGGGGGGATTTGCTTGGTCGGTTCT595'-AGCAGCACAGAGGTCAGATG-N59-TTCACGGTAGCACGCATAGG-3'ssDNACampylobacter JejuniWhole cellIdentify aptamers and develop a hetero-sandwich-based assay for colorimetric analysis of C. jejuni from contaminated samples.N/A12Fluorescence Binding Assay3.53 ± 1.38 nMDetectionWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1792 https://doi.org/10.1016/j.snb.2022.1328602023A HCR based multivalent aptamer amplifier for ultrasensitive detection of SalmonellaApt (mono-apt)GAGAGAGAATATAAGGGAAAAAAAAAAAAAAAAAAAAGTCAACACGAGAGGAGGGGAGTGGAATCAGGATAGGTGTGTAGGG82N/AssDNASalmonella Typhimurium (S. Typhimurium) (ATCC 14028)Whole cellDeveloped a hybridization chain reaction (HCR) based multivalent aptamer (multi-Apt) as an effective signal amplifier for the sensitive detection of Salmonella.N/AN/AEnzyme-Linked Immunosorbent Assay (ELISA)389.63 nM (with mono-apt)BiosensorN/A5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1793 https://doi.org/10.1016/j.snb.2022.1328602023A HCR based multivalent aptamer amplifier for ultrasensitive detection of SalmonellaApt1 (multi-apt)GAAGTGTACGTAGCCTGATTAAAAAAAAAAAAGTCAACACGAGAGGAGGGGAGTGGAATCAGGATAGGTGTGTAGGG77N/AssDNASalmonella Typhimurium (S. Typhimurium) (ATCC 14028)Whole cellDeveloped a hybridization chain reaction (HCR) based multivalent aptamer (multi-Apt) as an effective signal amplifier for the sensitive detection of Salmonella.Could detect Salmonella with multi-apt as low as 7 cfu/mL with a broad detection range of 10 to 10(7) cfu/mL.N/AEnzyme-Linked Immunosorbent Assay (ELISA)11.72 nM (with multi-apt)BiosensorN/A5'-Biotinylated and 5'-FAM LabeledN/AThe signals generated by the multi-Apt amplifier with different storage times at 4°C have remained unchanged over the past month.N/AN/AN/A
ABdb_1794 https://doi.org/10.1016/j.snb.2022.1328602023A HCR based multivalent aptamer amplifier for ultrasensitive detection of SalmonellaApt2 (multi-apt)TCGTCTACACTACTGCTCTTAAAAAAAAAAAAGTCAACACGAGAGGAGGGGAGTGGAATCAGGATAGGTGTGTAGGG77N/AssDNASalmonella Typhimurium (S. Typhimurium) (ATCC 14028)Whole cellDeveloped a hybridization chain reaction (HCR) based multivalent aptamer (multi-Apt) as an effective signal amplifier for the sensitive detection of Salmonella.Could detect Salmonella with multi-apt as low as 7 cfu/mL with a broad detection range of 10 to 10(7) cfu/mL.N/AEnzyme-Linked Immunosorbent Assay (ELISA)11.72 nM (with multi-apt)BiosensorN/A5'-Biotinylated and 5'-FAM LabeledN/AThe signals generated by the multi-Apt amplifier with different storage times at 4°C have remained unchanged over the past month.N/AN/AN/A
ABdb_1795 https://doi.org/10.1016/j.snb.2022.1328602023A HCR based multivalent aptamer amplifier for ultrasensitive detection of SalmonellaApt3 (multi-apt)TCTCCAATGACGTACCTGTTAAAAAAAAAAAAGTCAACACGAGAGGAGGGGAGTGGAATCAGGATAGGTGTGTAGGG77N/AssDNASalmonella Typhimurium (S. Typhimurium) (ATCC 14028)Whole cellDeveloped a hybridization chain reaction (HCR) based multivalent aptamer (multi-Apt) as an effective signal amplifier for the sensitive detection of Salmonella.Could detect Salmonella with multi-apt as low as 7 cfu/mL with a broad detection range of 10 to 10(7) cfu/mL.N/AEnzyme-Linked Immunosorbent Assay (ELISA)11.72 nM (with multi-apt)BiosensorN/A5'-Biotinylated and 5'-FAM LabeledN/AThe signals generated by the multi-Apt amplifier with different storage times at 4°C have remained unchanged over the past month.N/AN/AN/A
ABdb_1796 https://doi.org/10.1016/j.snb.2022.1328602023A HCR based multivalent aptamer amplifier for ultrasensitive detection of SalmonellaApt4 (multi-apt)GTTGCAGTACTCTACGAGTTAAAAAAAAAAAAGTCAACACGAGAGGAGGGGAGTGGAATCAGGATAGGTGTGTAGGG77N/AssDNASalmonella Typhimurium (S. Typhimurium) (ATCC 14028)Whole cellDeveloped a hybridization chain reaction (HCR) based multivalent aptamer (multi-Apt) as an effective signal amplifier for the sensitive detection of Salmonella.Could detect Salmonella with multi-apt as low as 7 cfu/mL with a broad detection range of 10 to 10(7) cfu/mL.N/AEnzyme-Linked Immunosorbent Assay (ELISA)11.72 nM (with multi-apt)BiosensorN/A5'-Biotinylated and 5'-FAM LabeledN/AThe signals generated by the multi-Apt amplifier with different storage times at 4°C have remained unchanged over the past month.N/AN/AN/A
ABdb_1797 https://doi.org/10.1016/j.snb.2022.1328602023A HCR based multivalent aptamer amplifier for ultrasensitive detection of SalmonellaApt5 (multi-apt)TGTACTGGACAAGTGACGTTAAAAAAAAAAAAGTCAACACGAGAGGAGGGGAGTGGAATCAGGATAGGTGTGTAGGG77N/AssDNASalmonella Typhimurium (S. Typhimurium) (ATCC 14028)Whole cellDeveloped a hybridization chain reaction (HCR) based multivalent aptamer (multi-Apt) as an effective signal amplifier for the sensitive detection of Salmonella.Could detect Salmonella with multi-apt as low as 7 cfu/mL with a broad detection range of 10 to 10(7) cfu/mL.N/AEnzyme-Linked Immunosorbent Assay (ELISA)11.72 nM (with multi-apt)BiosensorN/A5'-Biotinylated and 5'-FAM LabeledN/AThe signals generated by the multi-Apt amplifier with different storage times at 4°C have remained unchanged over the past month.N/AN/AN/A
ABdb_1884 404519602025Screening and characterization of nucleic acid aptamers targeting Brucella surface antigens: identification and analysis of their corresponding binding sitesWS-6GCTGCAATACTCATGGACAGCACGGCACGGGCTGTCGATCTCGAGGGAAACGGCACATGTGTCTGGAGTACGACCCTGAA80N/AssDNABrucella S2 vaccine strainOuter membrane protein BamA (β-barrel assembly machinery A)Identify aptamers against Brucella and conjugate them to liposomes for selective recognition and significantly reduced bacterial invasion of host cells.WS-6 significantly reduced Brucella invasion, as evidenced by a decrease in qPCR Ct from 22.34 to 20.64 (P < 0.05), confirming a reduced intracellular bacterial load.13Indirect Enzyme-Linked Aptamer Assay (i-ELAA)16.23 ± 5.84 nMTherapeuticsWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledN/AThe aptamer demonstrated stable binding to the Brucella S2 vaccine across a temperature range of 16–50°C, with optimal binding observed between 16°C and 50°C and under neutral conditions (pH 7.6) in 2h.Best CandidateN/AN/A
ABdb_1885 404519602025Screening and characterization of nucleic acid aptamers targeting Brucella surface antigens: identification and analysis of their corresponding binding sitesWS-26GCTGCAATACTCATGGACAGCGGAACGCTGTCTCCTCATTCAATCTAGGAGTCTGCGTGAGTCTGGAGTACGACCCTGAA80N/AssDNABrucella S2 vaccine strainWhole cellBinds BamA β-barrel assembly protein → blocks/inhibits bacterial invasion into host cells.N/A13Indirect Enzyme-Linked Aptamer Assay (i-ELAA)20.33 ± 8.12 nMTherapeuticsWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1886 404519602025Screening and characterization of nucleic acid aptamers targeting Brucella surface antigens: identification and analysis of their corresponding binding sitesWS-17GCTGCAATACTCATGGACAGGACAACGTCCTGTACCAGCGCTACGCCAGATCAGTTTTAGGTCTGGAGTACGACCCTGAA80N/AssDNABrucella S2 vaccine strainWhole cellBinds BamA β-barrel assembly protein → blocks/inhibits bacterial invasion into host cells.N/A13Indirect Enzyme-Linked Aptamer Assay (i-ELAA)17.11 ± 6.35 nMTherapeuticsWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1887 404519602025Screening and characterization of nucleic acid aptamers targeting Brucella surface antigens: identification and analysis of their corresponding binding sitesWS-32GCTGCAATACTCATGGACAGGGGACTCAGGTCCCCGGGAGCGCAATGGTGGGGTTTTAATGTCTGGAGTACGACCCTGAA80N/AssDNABrucella S2 vaccine strainWhole cellBinds BamA β-barrel assembly protein → blocks/inhibits bacterial invasion into host cells.N/A13Indirect Enzyme-Linked Aptamer Assay (i-ELAA)13.08 ± 2.97 nMTherapeuticsWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1888 404519602025Screening and characterization of nucleic acid aptamers targeting Brucella surface antigens: identification and analysis of their corresponding binding sitesWS-44GCTGCAATACTCATGGACAGGGACCTGTCCCTGGCCTCTTAGGGTAAAATTTTGCCACAAGTCTGGAGTACGACCCTGAA80N/AssDNABrucella S2 vaccine strainWhole cellBinds BamA β-barrel assembly protein → blocks/inhibits bacterial invasion into host cells.N/A13Indirect Enzyme-Linked Aptamer Assay (i-ELAA)15.03 ± 4.2 nMTherapeuticsWhole Cell-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1896 412051602025Selection of Ruthenium Polypyridyl Complex-Modified Aptamers for Photodynamic Therapy against Streptococcus PneumoniaS8CGTACGGTCGACGCTAGC-ACACCCCCCAGGATCATAAATTCTCTCGCTGTAGC-CACGTGGAGCTCGGATGC715'-CGTACGGTCGACGCTAGC-35N-CACGTGGAGCTCGGATGC-3'ssDNAStreptococcus Pneumoniae R6Whole cellAptamer-functionalized ruthenium polypyridyl complexes against S. pneumoniae with targeted photodynamic therapy (PDT).N/A10 rounds (with standard DNA chemistry) and 12 (for the mod-SELEX)Flow CytometryN/ADetectionSELEX and Mod-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1897 412051602025Selection of Ruthenium Polypyridyl Complex-Modified Aptamers for Photodynamic Therapy against Streptococcus PneumoniaS10CGTACGGTCGACGCTAGC-ACCAGCCATAGTCACATCAAAACTAACTCACATTC-CACGTGGAGCTCGGATGC715'-CGTACGGTCGACGCTAGC-35N-CACGTGGAGCTCGGATGC-3'ssDNAStreptococcus Pneumoniae R6Whole cellAptamer-functionalized ruthenium polypyridyl complexes against S. pneumoniae with targeted photodynamic therapy (PDT).N/A10 rounds (with standard DNA chemistry) and 12 (for the mod-SELEX)Flow CytometryN/ADetectionSELEX and Mod-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1898 412051602025Selection of Ruthenium Polypyridyl Complex-Modified Aptamers for Photodynamic Therapy against Streptococcus PneumoniaS12CGTACGGTCGACGCTAGC-CCCATACTCATCACCATTCACATCACTCACCTAGC-CACGTGGAGCTCGGATGC715'-CGTACGGTCGACGCTAGC-35N-CACGTGGAGCTCGGATGC-3'ssDNAStreptococcus Pneumoniae R6Whole cellAptamer-functionalized ruthenium polypyridyl complexes against S. pneumoniae with targeted photodynamic therapy (PDT).N/A10 rounds (with standard DNA chemistry) and 12 (for the mod-SELEX)Flow CytometryN/ADetectionSELEX and Mod-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1899 412051602025Selection of Ruthenium Polypyridyl Complex-Modified Aptamers for Photodynamic Therapy against Streptococcus PneumoniaS1GGATCCGAGCTCCACGTG-GCTAGGTGAGTGATGTGAATGGTGATGAGTATGGG-GCTAGCGTCGACCGTACG715'-CGTACGGTCGACGCTAGC-35N-CACGTGGAGCTCGGATGC-3'ssDNAStreptococcus Pneumoniae R6Whole cellAptamer-functionalized ruthenium polypyridyl complexes against S. pneumoniae with targeted photodynamic therapy (PDT).S1, the Ru-modified oligonucleotide, bound S. pneumoniae R6 with slightly lower affinity than S9.10 rounds (with standard DNA chemistry) and 12 (for the mod-SELEX)Flow Cytometry125 ± 91 nMDetectionSELEX and Mod-SELEXT=dURu(bpy)TP1, 5'-Biotinylated and 5'-FAM LabeledN/AN/ABest CandidateN/AN/A
ABdb_1900 412051602025Selection of Ruthenium Polypyridyl Complex-Modified Aptamers for Photodynamic Therapy against Streptococcus PneumoniaS9ACACCCCCCAGGATCATAAATTCTCTCGCTGTAGC355'-CGTACGGTCGACGCTAGC-35N-CACGTGGAGCTCGGATGC-3'ssDNAStreptococcus Pneumoniae R6Whole cellAptamer-functionalized ruthenium polypyridyl complexes against S. pneumoniae with targeted photodynamic therapy (PDT).S9 bound better to the bacterial target than the modified sequence S1.10 rounds (with standard DNA chemistry) and 12 (for the mod-SELEX)Flow Cytometry118 ± 1 nMDetectionSELEX and Mod-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/ABest CandidateN/AN/A
ABdb_1901 412051602025Selection of Ruthenium Polypyridyl Complex-Modified Aptamers for Photodynamic Therapy against Streptococcus PneumoniaS11ACCAGCCATAGTCACATCAAAACTAACTCACATTC355'-CGTACGGTCGACGCTAGC-35N-CACGTGGAGCTCGGATGC-3'ssDNAStreptococcus Pneumoniae R6Whole cellAptamer-functionalized ruthenium polypyridyl complexes against S. pneumoniae with targeted photodynamic therapy (PDT).S11 exhibited a lower propensity at binding to the bacterial target.10 rounds (with standard DNA chemistry) and 12 (for the mod-SELEX)Flow Cytometry541 ± 1 nMDetectionSELEX and Mod-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A
ABdb_1902 412051602025Selection of Ruthenium Polypyridyl Complex-Modified Aptamers for Photodynamic Therapy against Streptococcus PneumoniaS13CCCATACTCATCACCATTCACATCACTCACCTAGC355'-CGTACGGTCGACGCTAGC-35N-CACGTGGAGCTCGGATGC-3'ssDNAStreptococcus Pneumoniae R6Whole cellAptamer-functionalized ruthenium polypyridyl complexes against S. pneumoniae with targeted photodynamic therapy (PDT).N/A10 rounds (with standard DNA chemistry) and 12 (for the mod-SELEX)Flow CytometryN/ADetectionSELEX and Mod-SELEX5'-Biotinylated and 5'-FAM LabeledN/AN/AN/AN/AN/A