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sterile pbs  (Thermo Fisher)


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    Thermo Fisher sterile pbs
    Preparation and characterization of monoclonal antibodies <t>against</t> <t>GoAstV-2</t> VP27 protein. (A) Schematic of the immunization of mice with purified recombinant VP27 protein. The red blood drop symbols represent the time points when serum samples were collected, the notation for splenocytes indicates the time point at which the spleens were aseptically harvested. (B) The serum titers of four mice were measured by indirect ELISA. Control: negative mice immunized with <t>PBS.</t> (C) The reactivity of mAb 11-39B was tested in VP27 protein-based indirect ELISA. The cell supernatant of hybridoma clones 11-39B was used as the primary antibodies, the SP2/0 cell supernatant was used as the negative control. (D) Identification of the subtypes of mAb 11-39B. (E) Antibodies were purified using a protein G column and analyzed by SDS-PAGE. M, protein marker; Lane 1, crude ascites; Lane 2, loaded fraction; Lanes 3-4, wash fraction; Lanes 5-6, eluent fraction. (F) Measurement of the titers of ascites mAb 11-39B by VP27 protein-based indirect ELISA.
    Sterile Pbs, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 88582 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/sterile pbs/product/Thermo Fisher
    Average 99 stars, based on 88582 article reviews
    sterile pbs - by Bioz Stars, 2026-02
    99/100 stars

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    1) Product Images from "Development of monoclonal antibodies for GoAstV-2 VP27 protein and precise mapping of linear antigenic epitopes"

    Article Title: Development of monoclonal antibodies for GoAstV-2 VP27 protein and precise mapping of linear antigenic epitopes

    Journal: Poultry Science

    doi: 10.1016/j.psj.2026.106535

    Preparation and characterization of monoclonal antibodies against GoAstV-2 VP27 protein. (A) Schematic of the immunization of mice with purified recombinant VP27 protein. The red blood drop symbols represent the time points when serum samples were collected, the notation for splenocytes indicates the time point at which the spleens were aseptically harvested. (B) The serum titers of four mice were measured by indirect ELISA. Control: negative mice immunized with PBS. (C) The reactivity of mAb 11-39B was tested in VP27 protein-based indirect ELISA. The cell supernatant of hybridoma clones 11-39B was used as the primary antibodies, the SP2/0 cell supernatant was used as the negative control. (D) Identification of the subtypes of mAb 11-39B. (E) Antibodies were purified using a protein G column and analyzed by SDS-PAGE. M, protein marker; Lane 1, crude ascites; Lane 2, loaded fraction; Lanes 3-4, wash fraction; Lanes 5-6, eluent fraction. (F) Measurement of the titers of ascites mAb 11-39B by VP27 protein-based indirect ELISA.
    Figure Legend Snippet: Preparation and characterization of monoclonal antibodies against GoAstV-2 VP27 protein. (A) Schematic of the immunization of mice with purified recombinant VP27 protein. The red blood drop symbols represent the time points when serum samples were collected, the notation for splenocytes indicates the time point at which the spleens were aseptically harvested. (B) The serum titers of four mice were measured by indirect ELISA. Control: negative mice immunized with PBS. (C) The reactivity of mAb 11-39B was tested in VP27 protein-based indirect ELISA. The cell supernatant of hybridoma clones 11-39B was used as the primary antibodies, the SP2/0 cell supernatant was used as the negative control. (D) Identification of the subtypes of mAb 11-39B. (E) Antibodies were purified using a protein G column and analyzed by SDS-PAGE. M, protein marker; Lane 1, crude ascites; Lane 2, loaded fraction; Lanes 3-4, wash fraction; Lanes 5-6, eluent fraction. (F) Measurement of the titers of ascites mAb 11-39B by VP27 protein-based indirect ELISA.

    Techniques Used: Bioprocessing, Purification, Recombinant, Indirect ELISA, Control, Clone Assay, Negative Control, SDS Page, Marker



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    Preparation and characterization of monoclonal antibodies <t>against</t> <t>GoAstV-2</t> VP27 protein. (A) Schematic of the immunization of mice with purified recombinant VP27 protein. The red blood drop symbols represent the time points when serum samples were collected, the notation for splenocytes indicates the time point at which the spleens were aseptically harvested. (B) The serum titers of four mice were measured by indirect ELISA. Control: negative mice immunized with <t>PBS.</t> (C) The reactivity of mAb 11-39B was tested in VP27 protein-based indirect ELISA. The cell supernatant of hybridoma clones 11-39B was used as the primary antibodies, the SP2/0 cell supernatant was used as the negative control. (D) Identification of the subtypes of mAb 11-39B. (E) Antibodies were purified using a protein G column and analyzed by SDS-PAGE. M, protein marker; Lane 1, crude ascites; Lane 2, loaded fraction; Lanes 3-4, wash fraction; Lanes 5-6, eluent fraction. (F) Measurement of the titers of ascites mAb 11-39B by VP27 protein-based indirect ELISA.
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    Preparation and characterization of monoclonal antibodies against GoAstV-2 VP27 protein. (A) Schematic of the immunization of mice with purified recombinant VP27 protein. The red blood drop symbols represent the time points when serum samples were collected, the notation for splenocytes indicates the time point at which the spleens were aseptically harvested. (B) The serum titers of four mice were measured by indirect ELISA. Control: negative mice immunized with PBS. (C) The reactivity of mAb 11-39B was tested in VP27 protein-based indirect ELISA. The cell supernatant of hybridoma clones 11-39B was used as the primary antibodies, the SP2/0 cell supernatant was used as the negative control. (D) Identification of the subtypes of mAb 11-39B. (E) Antibodies were purified using a protein G column and analyzed by SDS-PAGE. M, protein marker; Lane 1, crude ascites; Lane 2, loaded fraction; Lanes 3-4, wash fraction; Lanes 5-6, eluent fraction. (F) Measurement of the titers of ascites mAb 11-39B by VP27 protein-based indirect ELISA.

    Journal: Poultry Science

    Article Title: Development of monoclonal antibodies for GoAstV-2 VP27 protein and precise mapping of linear antigenic epitopes

    doi: 10.1016/j.psj.2026.106535

    Figure Lengend Snippet: Preparation and characterization of monoclonal antibodies against GoAstV-2 VP27 protein. (A) Schematic of the immunization of mice with purified recombinant VP27 protein. The red blood drop symbols represent the time points when serum samples were collected, the notation for splenocytes indicates the time point at which the spleens were aseptically harvested. (B) The serum titers of four mice were measured by indirect ELISA. Control: negative mice immunized with PBS. (C) The reactivity of mAb 11-39B was tested in VP27 protein-based indirect ELISA. The cell supernatant of hybridoma clones 11-39B was used as the primary antibodies, the SP2/0 cell supernatant was used as the negative control. (D) Identification of the subtypes of mAb 11-39B. (E) Antibodies were purified using a protein G column and analyzed by SDS-PAGE. M, protein marker; Lane 1, crude ascites; Lane 2, loaded fraction; Lanes 3-4, wash fraction; Lanes 5-6, eluent fraction. (F) Measurement of the titers of ascites mAb 11-39B by VP27 protein-based indirect ELISA.

    Article Snippet: Simultaneously, the mock-infected group was inoculated with 1 mL sterile PBS; the virus-infected group was inoculated with 0.5 mL of GoAstV-2 solution (10 5.167 ELD 50 /0.5 mL) and 0.5 mL sterile PBS containing 200 μg/mL mouse IgG control (Thermo Fisher Scientific, USA).

    Techniques: Bioprocessing, Purification, Recombinant, Indirect ELISA, Control, Clone Assay, Negative Control, SDS Page, Marker