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Pepscan Inc epitope mapping
Epitope Mapping, supplied by Pepscan Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/epitope+mapping/epitope+mapping/pm40560613-66-0-0
Average 90 stars, based on 1 article reviews
epitope mapping - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

Sequencing:

Article Title: Anti-netrin-1 antibody
Article Snippet: .. Pepscan epitope mapping using the spot array of 590 15-amino acid linear peptides covering the whole sequence of human NET1. .. As shown in FIG. 9, the antibody HUM03 binds 8 overlapping peptides corresponding to the amino acid sequence “ARRCRFNMELYKLSGRKSGGVC” (SEQ ID NO: 35) which is present within the V-2 domain of NET1.

other:

Article Title: Monoclonal antibodies against Ambra-1
Article Snippet: Epitopes of Ambra-1 recognized by anti-Ambra-1 antibodies were mapped using linear, conformational and replacement analysis epitope mapping (Pepscan Presto BV) using established techniques (Timmerman et al (2007).

Article Title: Monoclonal antibodies against Ambra-1
Article Snippet: Epitopes of Loricrin recognized by anti-Loricrin antibodies were mapped using linear, conformational and replacement analysis epitope mapping (Pepscan Presto BV) using established techniques (Timmerman et al (2007).

Binding Assay:

Article Title: Ena/VASP-EVH1 inhibition prevents chemotaxis and metastasis by blocking the EVH1-WAVE2 interaction.
Article Snippet: .. Pepscan epitope mapping of WAVE2 binding to GST-VASP-EVH1 revealed a specific 15-mer WAVE2-derived peptide (SI Appendix, Fig. S1 ) that is conserved among different vertebrate species (SI Appendix, Table S2 ), but is absent in WAVE1 and WAVE3. ..



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Fig. 1 Schematic representation of synuclein proteins (α, β, and γ-synuclein) illustrating their conserved and unique epitopes. The lower panel shows the results of the β-syn-targeting ELISAs: N-terminus assay (using an EP1537Y antibody for detection and N-terminus capture), mid-region assay (utilizing EP1537Y and ADx <t>β-syn1</t> <t>antibodies),</t> and C-terminus assay (using EP1537Y for detection of ADx β-syn2 for capture). The placement of antibodies reflects their approximate binding sites on the β-syn protein. These in-house β-syn-specific assays offer targeted <t>epitope</t> recognition, enhancing the specificity of synaptic degeneration biomarker detection in AD. The exact binding epitopes of the antibodies are listed in the figure, starting with the first amino acid binding position and ending with the last amino acid
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Fig. 1 Schematic representation of synuclein proteins (α, β, and γ-synuclein) illustrating their conserved and unique epitopes. The lower panel shows the results of the β-syn-targeting ELISAs: N-terminus assay (using an EP1537Y antibody for detection and N-terminus capture), mid-region assay (utilizing EP1537Y and ADx <t>β-syn1</t> <t>antibodies),</t> and C-terminus assay (using EP1537Y for detection of ADx β-syn2 for capture). The placement of antibodies reflects their approximate binding sites on the β-syn protein. These in-house β-syn-specific assays offer targeted <t>epitope</t> recognition, enhancing the specificity of synaptic degeneration biomarker detection in AD. The exact binding epitopes of the antibodies are listed in the figure, starting with the first amino acid binding position and ending with the last amino acid
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Image Search Results


Fig. 1 Schematic representation of synuclein proteins (α, β, and γ-synuclein) illustrating their conserved and unique epitopes. The lower panel shows the results of the β-syn-targeting ELISAs: N-terminus assay (using an EP1537Y antibody for detection and N-terminus capture), mid-region assay (utilizing EP1537Y and ADx β-syn1 antibodies), and C-terminus assay (using EP1537Y for detection of ADx β-syn2 for capture). The placement of antibodies reflects their approximate binding sites on the β-syn protein. These in-house β-syn-specific assays offer targeted epitope recognition, enhancing the specificity of synaptic degeneration biomarker detection in AD. The exact binding epitopes of the antibodies are listed in the figure, starting with the first amino acid binding position and ending with the last amino acid

Journal: Alzheimer's research & therapy

Article Title: Novel CSF β-synuclein-specific assays signal early synaptic degeneration in Alzheimer's disease.

doi: 10.1186/s13195-025-01716-8

Figure Lengend Snippet: Fig. 1 Schematic representation of synuclein proteins (α, β, and γ-synuclein) illustrating their conserved and unique epitopes. The lower panel shows the results of the β-syn-targeting ELISAs: N-terminus assay (using an EP1537Y antibody for detection and N-terminus capture), mid-region assay (utilizing EP1537Y and ADx β-syn1 antibodies), and C-terminus assay (using EP1537Y for detection of ADx β-syn2 for capture). The placement of antibodies reflects their approximate binding sites on the β-syn protein. These in-house β-syn-specific assays offer targeted epitope recognition, enhancing the specificity of synaptic degeneration biomarker detection in AD. The exact binding epitopes of the antibodies are listed in the figure, starting with the first amino acid binding position and ending with the last amino acid

Article Snippet: Linear epitope mapping of two rabbit monoclonal antibodies, EP1537Y (Abcam, ab221908) and EP1646Y (Abcam, ab189217), and two mouse monoclonal antibodies, ADx β-syn1 and ADx β-syn2, was conducted using three libraries of overlapping synthetic peptides (BioSynth, Lelystadt, NL) [34].

Techniques: Binding Assay, Biomarker Discovery