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peptide microarray for epitope mapping  (Abnova)

 
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    Abnova peptide microarray for epitope mapping
    Peptide Microarray For Epitope Mapping, supplied by Abnova, 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/peptide+microarray+epitope+mapping/peptide+microarray+epitope+mapping/pm25942475-167-8-13
    Average 90 stars, based on 1 article reviews
    peptide microarray for epitope mapping - by Bioz Stars, 2026-09
    90/100 stars

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    Peptide Microarray:

    Article Title: TTAC-0001, a human monoclonal antibody targeting VEGFR-2/KDR, blocks tumor angiogenesis
    Article Snippet: Peptide microarray of epitope mapping Peptide microarray for epitope mapping was done by Abnova (Taipei city, Taiwan). .. Peptide microarray of epitope mapping Peptide microarray for epitope mapping was done by Abnova (Taipei city, Taiwan). .. The determination of peptide-antibody binding was performed by PepStar-analysis where the peptide microarray was incubated with TTAC-0001 or control human IgG (Pierce #31154) followed by a Dylight-649 labeled secondary antibody (Pierce #35515) directed against the Fc-part of the primary one.



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    peptide microarray epitope mapping  (Abnova)
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    Domain and <t>epitope</t> mapping of anti-KDR antibodies. (a) Domain mapping analysis of anti-KDR antibodies on the extracellular region of KDR. Black bar represents extracellular domain 1 and 2 of KDR (KDR (ECD 1–2)). Gray bar represents extracellular domain 2 and 3 of KDR (KDR (ECD 2–3)). White bar represents extracellular domain 1, 2 and 3 of KDR (KDR (ECD 1–3)). (b) <t>Peptide</t> <t>microarray</t> for epitope mapping. As an antigen, KDR (ECD1–3) was used. The sequence was scanned with a format of 13meric peptides overlapping 11 amino acid residues with the following peptide, resulting in a total of 149 peptides. The binding of primary antibody (TTAC-0001, control human IgG) to the peptide was measured with dylight-649 labeled secondary antibody. Left panel: Fluorescence intensity of peptide. The intensity of fluorescence measured by TTAC-0001 was subtracted the value of control human IgG (Pierce). Arrows indicate peptides showing over 10,000 LU of signal intensity. Right panel: Amino acid sequence (peptide i.d.) showed high intensity of fluorescence (≥ 10,000 LU). The sequences inside the box indicate epitopes for TTAC-0001.
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    Domain and <t>epitope</t> mapping of anti-KDR antibodies. (a) Domain mapping analysis of anti-KDR antibodies on the extracellular region of KDR. Black bar represents extracellular domain 1 and 2 of KDR (KDR (ECD 1–2)). Gray bar represents extracellular domain 2 and 3 of KDR (KDR (ECD 2–3)). White bar represents extracellular domain 1, 2 and 3 of KDR (KDR (ECD 1–3)). (b) <t>Peptide</t> <t>microarray</t> for epitope mapping. As an antigen, KDR (ECD1–3) was used. The sequence was scanned with a format of 13meric peptides overlapping 11 amino acid residues with the following peptide, resulting in a total of 149 peptides. The binding of primary antibody (TTAC-0001, control human IgG) to the peptide was measured with dylight-649 labeled secondary antibody. Left panel: Fluorescence intensity of peptide. The intensity of fluorescence measured by TTAC-0001 was subtracted the value of control human IgG (Pierce). Arrows indicate peptides showing over 10,000 LU of signal intensity. Right panel: Amino acid sequence (peptide i.d.) showed high intensity of fluorescence (≥ 10,000 LU). The sequences inside the box indicate epitopes for TTAC-0001.
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    Domain and epitope mapping of anti-KDR antibodies. (a) Domain mapping analysis of anti-KDR antibodies on the extracellular region of KDR. Black bar represents extracellular domain 1 and 2 of KDR (KDR (ECD 1–2)). Gray bar represents extracellular domain 2 and 3 of KDR (KDR (ECD 2–3)). White bar represents extracellular domain 1, 2 and 3 of KDR (KDR (ECD 1–3)). (b) Peptide microarray for epitope mapping. As an antigen, KDR (ECD1–3) was used. The sequence was scanned with a format of 13meric peptides overlapping 11 amino acid residues with the following peptide, resulting in a total of 149 peptides. The binding of primary antibody (TTAC-0001, control human IgG) to the peptide was measured with dylight-649 labeled secondary antibody. Left panel: Fluorescence intensity of peptide. The intensity of fluorescence measured by TTAC-0001 was subtracted the value of control human IgG (Pierce). Arrows indicate peptides showing over 10,000 LU of signal intensity. Right panel: Amino acid sequence (peptide i.d.) showed high intensity of fluorescence (≥ 10,000 LU). The sequences inside the box indicate epitopes for TTAC-0001.

    Journal: mAbs

    Article Title: TTAC-0001, a human monoclonal antibody targeting VEGFR-2/KDR, blocks tumor angiogenesis

    doi: 10.1080/19420862.2015.1045168

    Figure Lengend Snippet: Domain and epitope mapping of anti-KDR antibodies. (a) Domain mapping analysis of anti-KDR antibodies on the extracellular region of KDR. Black bar represents extracellular domain 1 and 2 of KDR (KDR (ECD 1–2)). Gray bar represents extracellular domain 2 and 3 of KDR (KDR (ECD 2–3)). White bar represents extracellular domain 1, 2 and 3 of KDR (KDR (ECD 1–3)). (b) Peptide microarray for epitope mapping. As an antigen, KDR (ECD1–3) was used. The sequence was scanned with a format of 13meric peptides overlapping 11 amino acid residues with the following peptide, resulting in a total of 149 peptides. The binding of primary antibody (TTAC-0001, control human IgG) to the peptide was measured with dylight-649 labeled secondary antibody. Left panel: Fluorescence intensity of peptide. The intensity of fluorescence measured by TTAC-0001 was subtracted the value of control human IgG (Pierce). Arrows indicate peptides showing over 10,000 LU of signal intensity. Right panel: Amino acid sequence (peptide i.d.) showed high intensity of fluorescence (≥ 10,000 LU). The sequences inside the box indicate epitopes for TTAC-0001.

    Article Snippet: Peptide microarray of epitope mapping Peptide microarray for epitope mapping was done by Abnova (Taipei city, Taiwan).

    Techniques: Peptide Microarray, Sequencing, Binding Assay, Control, Labeling, Fluorescence