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mouse monoclonal antibodies against human cd26  (Thermo Fisher)


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    Structured Review

    Thermo Fisher mouse monoclonal antibodies against human cd26
    Peptide Matches from Tandem Mass Spectrometry of Proteins Purified by Lactose Affinity Chromatography of Human Prostasomes
    Mouse Monoclonal Antibodies Against Human Cd26, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse monoclonal antibodies against human cd26/product/Thermo Fisher
    Average 86 stars, based on 1 article reviews
    mouse monoclonal antibodies against human cd26 - by Bioz Stars, 2026-02
    86/100 stars

    Images

    1) Product Images from "Co-Purification of Mac-2 Binding Protein with Galectin-3 and Association with Prostasomes in Human Semen"

    Article Title: Co-Purification of Mac-2 Binding Protein with Galectin-3 and Association with Prostasomes in Human Semen

    Journal:

    doi: 10.1002/pros.21287

    Peptide Matches from Tandem Mass Spectrometry of Proteins Purified by Lactose Affinity Chromatography of Human Prostasomes
    Figure Legend Snippet: Peptide Matches from Tandem Mass Spectrometry of Proteins Purified by Lactose Affinity Chromatography of Human Prostasomes

    Techniques Used: Mass Spectrometry, Purification, Affinity Chromatography, Sequencing, Binding Assay

    Protein-protein interaction network of the identified proteins. Cytoscape was used to display the protein-protein interaction map generated from interaction database data pulled down from the HPRD, BioGRID, IntAct, and NCI/Nature Pathway Interaction databases. White nodes indicate the proteins identified in this study following β-galactoside affinity purification. Gray nodes indicate interacting proteins retrieved from the databases. Connecting lines indicate identified protein interactions. Each protein is shown by its gene symbol or entrez identification number. Galectin-3 (LGALS3), M2BP (LGALS3BP), lactoferrin (LTF), PIP (PIP), CD26 (DPP4), seminogelin I (SEMG1), seminogelin 2 (SEMG2), olfactomedin 4 (OLFM4).
    Figure Legend Snippet: Protein-protein interaction network of the identified proteins. Cytoscape was used to display the protein-protein interaction map generated from interaction database data pulled down from the HPRD, BioGRID, IntAct, and NCI/Nature Pathway Interaction databases. White nodes indicate the proteins identified in this study following β-galactoside affinity purification. Gray nodes indicate interacting proteins retrieved from the databases. Connecting lines indicate identified protein interactions. Each protein is shown by its gene symbol or entrez identification number. Galectin-3 (LGALS3), M2BP (LGALS3BP), lactoferrin (LTF), PIP (PIP), CD26 (DPP4), seminogelin I (SEMG1), seminogelin 2 (SEMG2), olfactomedin 4 (OLFM4).

    Techniques Used: Generated, Affinity Purification

    Prostasome purification by size exclusion chromatography and M2BP immunoblot analysis. The membrane fraction from seminal plasma was subjected to size exclusion column chromatography on Sephacryl S300 and prostasomes were collected in the void volume (fractions 14-19). Electroblots of collected fractions were stained for total protein with Ponceau S and for M2BP (R&D polyclonal antibodies) and CD26 immunoreactivity. Molecular weight markers are indicated in kDa.
    Figure Legend Snippet: Prostasome purification by size exclusion chromatography and M2BP immunoblot analysis. The membrane fraction from seminal plasma was subjected to size exclusion column chromatography on Sephacryl S300 and prostasomes were collected in the void volume (fractions 14-19). Electroblots of collected fractions were stained for total protein with Ponceau S and for M2BP (R&D polyclonal antibodies) and CD26 immunoreactivity. Molecular weight markers are indicated in kDa.

    Techniques Used: Purification, Size-exclusion Chromatography, Western Blot, Column Chromatography, Staining, Molecular Weight



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    Image Search Results


    Peptide Matches from Tandem Mass Spectrometry of Proteins Purified by Lactose Affinity Chromatography of Human Prostasomes

    Journal:

    Article Title: Co-Purification of Mac-2 Binding Protein with Galectin-3 and Association with Prostasomes in Human Semen

    doi: 10.1002/pros.21287

    Figure Lengend Snippet: Peptide Matches from Tandem Mass Spectrometry of Proteins Purified by Lactose Affinity Chromatography of Human Prostasomes

    Article Snippet: Mouse monoclonal antibodies against human CD26 were from Lab Vision (Fremont, CA).

    Techniques: Mass Spectrometry, Purification, Affinity Chromatography, Sequencing, Binding Assay

    Protein-protein interaction network of the identified proteins. Cytoscape was used to display the protein-protein interaction map generated from interaction database data pulled down from the HPRD, BioGRID, IntAct, and NCI/Nature Pathway Interaction databases. White nodes indicate the proteins identified in this study following β-galactoside affinity purification. Gray nodes indicate interacting proteins retrieved from the databases. Connecting lines indicate identified protein interactions. Each protein is shown by its gene symbol or entrez identification number. Galectin-3 (LGALS3), M2BP (LGALS3BP), lactoferrin (LTF), PIP (PIP), CD26 (DPP4), seminogelin I (SEMG1), seminogelin 2 (SEMG2), olfactomedin 4 (OLFM4).

    Journal:

    Article Title: Co-Purification of Mac-2 Binding Protein with Galectin-3 and Association with Prostasomes in Human Semen

    doi: 10.1002/pros.21287

    Figure Lengend Snippet: Protein-protein interaction network of the identified proteins. Cytoscape was used to display the protein-protein interaction map generated from interaction database data pulled down from the HPRD, BioGRID, IntAct, and NCI/Nature Pathway Interaction databases. White nodes indicate the proteins identified in this study following β-galactoside affinity purification. Gray nodes indicate interacting proteins retrieved from the databases. Connecting lines indicate identified protein interactions. Each protein is shown by its gene symbol or entrez identification number. Galectin-3 (LGALS3), M2BP (LGALS3BP), lactoferrin (LTF), PIP (PIP), CD26 (DPP4), seminogelin I (SEMG1), seminogelin 2 (SEMG2), olfactomedin 4 (OLFM4).

    Article Snippet: Mouse monoclonal antibodies against human CD26 were from Lab Vision (Fremont, CA).

    Techniques: Generated, Affinity Purification

    Prostasome purification by size exclusion chromatography and M2BP immunoblot analysis. The membrane fraction from seminal plasma was subjected to size exclusion column chromatography on Sephacryl S300 and prostasomes were collected in the void volume (fractions 14-19). Electroblots of collected fractions were stained for total protein with Ponceau S and for M2BP (R&D polyclonal antibodies) and CD26 immunoreactivity. Molecular weight markers are indicated in kDa.

    Journal:

    Article Title: Co-Purification of Mac-2 Binding Protein with Galectin-3 and Association with Prostasomes in Human Semen

    doi: 10.1002/pros.21287

    Figure Lengend Snippet: Prostasome purification by size exclusion chromatography and M2BP immunoblot analysis. The membrane fraction from seminal plasma was subjected to size exclusion column chromatography on Sephacryl S300 and prostasomes were collected in the void volume (fractions 14-19). Electroblots of collected fractions were stained for total protein with Ponceau S and for M2BP (R&D polyclonal antibodies) and CD26 immunoreactivity. Molecular weight markers are indicated in kDa.

    Article Snippet: Mouse monoclonal antibodies against human CD26 were from Lab Vision (Fremont, CA).

    Techniques: Purification, Size-exclusion Chromatography, Western Blot, Column Chromatography, Staining, Molecular Weight