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monomeric recombinant human full length antigen  (R&D Systems)


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    Structured Review

    R&D Systems monomeric recombinant human full length antigen
    Monomeric Recombinant Human Full Length Antigen, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/301-R3/Recombinant+Human+IL-3R+alpha%2FCD123+Protein/pm39870691-212-3-10
    Average 93 stars, based on 8 article reviews
    monomeric recombinant human full length antigen - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Recombinant:

    Article Title: A novel label-free method to determine equilibrium dissociation constants of antibodies binding to cell surface proteins.
    Article Snippet: For generation of monoclonal anti-CD3 antibodies, monoclonal antibody SP34, mouse IgG3/lambda isotype (BD Biosciences, Pharmingen, 556,611) and monoclonal antibody, SP34-2, mouse IgG1/lambda isotype (BD Biosciences, Pharmingen, 551,916) were purchased. .. Recombinant CD123 proteins and anti-CD123 Fab Recombinant human CD123 SP1 ECD-His tag protein was obtained from R&D Systems (301-R3/CF, lot# LV081110A). .. Recombinant human CD123 SP2 ECD-His tagged protein was purified from baculovirus (custom produced by BlueSky in High 5 cells, Lot #120,503-CP05057h or lot 6519A).

    Article Title: A novel label-free method to determine equilibrium dissociation constants of antibodies binding to cell surface proteins.
    Article Snippet: .. Following antibody capture, monomeric recombinant human full-length antigen (huCD123 SP1, R&D Systems cat 301-R3/CF, lot# LV091112A or LV081110A) or truncated antigen-variant (huCD123 SP2, BlueSky Lot #120,503-CP05057h or 6519A) in solution (1.6 nM to 400 nM with fourfold dilutions) were injected.The association was monitored for 3 min (120 μL injected at 40 μL/min) and dissociation was monitored for 10 min. Regeneration of the sensor surface was achieved with a 20 s injection of 0.85% H3PO4 followed by 20 s injection of 50 mM NaOH. .. Data were processed using the Biacore T200 V2.0 evaluation software or the Biaevaluation software V4.0.1 for Biacore 3000 data.

    Article Title: A novel label-free method to determine equilibrium dissociation constants of antibodies binding to cell surface proteins.
    Article Snippet: .. For generation of monoclonal anti-CD123 antibodies, recombinant human CD123 SP1 ECD-His tag protein (R&D Systems, 301-R3/CF, lot# LV081110A) was used for phage panning and hit screening. ..

    Article Title: Impact of scFv on Functionality and Safety of Third-Generation CD123 CAR T Cells.
    Article Snippet: .. Briefly, five Balb/c mice were immunized five times in a foot pad with 1 μg/mouse of recombinant human CD123 (R&D Systems, Cat# 301-R3-025/CF). .. Two Balb/c mice were immunized four times through intraperitoneal injection with 10 μg/ mouse of recombinant human CD123 (R&D Systems, Cat# 301-R3025/CF) and one boost intravenously.

    Article Title: Impact of scFv on Functionality and Safety of Third-Generation CD123 CAR T Cells.
    Article Snippet: .. Briefly, recombinant human CD123 protein (R&D Systems, Cat# 301-R3) was tested at 100 nmol/L diluted by one-half at seven spots and the five antibodies at 20 μg/mL (Diaclone, Besançon). ..

    Article Title: Impact of scFv on Functionality and Safety of Third-Generation CD123 CAR T Cells.
    Article Snippet: Briefly, five Balb/c mice were immunized five times in a foot pad with 1 μg/mouse of recombinant human CD123 (R&D Systems, Cat# 301-R3-025/CF). .. Two Balb/c mice were immunized four times through intraperitoneal injection with 10 μg/ mouse of recombinant human CD123 (R&D Systems, Cat# 301-R3025/CF) and one boost intravenously. ..

    Article Title: Impact of scFv on Functionality and Safety of Third-Generation CD123 CAR T Cells.
    Article Snippet: In the case of cells derived from the peripheral blood or bone marrow of mice, cells were labeled and incubated with coupled antibodies before lysis of the red blood cells (BD Biosciences, Cat# 349202), washed, and analyzed via FC. .. Materials and reagents with respective vendors were as follows: from Miltenyi Biotec, CD3-VioBlue (Cat# 130-113-133; RRID: AB_10831672), CD19-APC (Cat# 130-113-165; RRID: AB_2725993), and running buffer (Cat# 130-091-221); from Sony Biotechnology, CD4-PE/Cy7 (Cat# 2387050), CD8-FITC (Cat# 2323520), CD123-PE/Cy7 (Cat# 2130050), 7-AAD Viability Staining Solution (Cat# 2702020), CD45-Brilliant Violet 510 (Cat# 2120180), CD45-APC (Cat# 1338540), CD19-APC (Cat# 2111060), CD14APC/Cy7 (Cat# 2435540), CD303-FITC (Cat# 2371040), and CD19PE (Cat# 2111040); from Invitrogen, Monensin Solution (Cat# 00- 4505-51) and eBioscience Cell Proliferation Dye eFluor 450 (Cat# 65-0863); from BD Pharmingen, CD33-PE (Cat# 345799; RRID: AB_2868826), HLA-DR-PerCP-Cy5.5 (Cat# 560652; RRID: AB_1727529), CD34-APC (Cat# 555824; RRID: AB_398614), CD38-APC-H7 (Cat# 656646; RRID: AB_2870413), CD107a-FITC OF2 Cancer Immunol Res; 2024 CANCER IMMUNOLOGY RESEARCH Fredon et al. D ow nloaded from http://aacrjournals.org/cancerim m unolres/article-pdf/doi/10.1158/2326-6066.C IR -23-0548/3463330/cir-23-0548.pdf by IN SER M user on 20 June 2024 (Cat# 555800; RRID: AB_396134), and Streptavidin-APC (Cat# 554067; RRID AB_10050396); from BD Biosciences, Trucount Absolute Counting Tubes IVD (Cat# 663028); and from R&D Systems, recombinant human IL3R alpha/CD123 protein (Cat# 301-R2-025). .. Determination of the absolute number of CD123 antigenic sites on Gen2.2, CAL1, MA-9-RAS, HMEC1, and Daudi cell lines as well as on primary CD34+ and CD14+ cells was done using indirect immunofluorescence FC using Mouse IgG Calibrator (BioCytex, Cat# CP051).

    Injection:

    Article Title: A novel label-free method to determine equilibrium dissociation constants of antibodies binding to cell surface proteins.
    Article Snippet: .. Following antibody capture, monomeric recombinant human full-length antigen (huCD123 SP1, R&D Systems cat 301-R3/CF, lot# LV091112A or LV081110A) or truncated antigen-variant (huCD123 SP2, BlueSky Lot #120,503-CP05057h or 6519A) in solution (1.6 nM to 400 nM with fourfold dilutions) were injected.The association was monitored for 3 min (120 μL injected at 40 μL/min) and dissociation was monitored for 10 min. Regeneration of the sensor surface was achieved with a 20 s injection of 0.85% H3PO4 followed by 20 s injection of 50 mM NaOH. .. Data were processed using the Biacore T200 V2.0 evaluation software or the Biaevaluation software V4.0.1 for Biacore 3000 data.

    Article Title: Impact of scFv on Functionality and Safety of Third-Generation CD123 CAR T Cells.
    Article Snippet: Briefly, five Balb/c mice were immunized five times in a foot pad with 1 μg/mouse of recombinant human CD123 (R&D Systems, Cat# 301-R3-025/CF). .. Two Balb/c mice were immunized four times through intraperitoneal injection with 10 μg/ mouse of recombinant human CD123 (R&D Systems, Cat# 301-R3025/CF) and one boost intravenously. ..

    Staining:

    Article Title: Impact of scFv on Functionality and Safety of Third-Generation CD123 CAR T Cells.
    Article Snippet: In the case of cells derived from the peripheral blood or bone marrow of mice, cells were labeled and incubated with coupled antibodies before lysis of the red blood cells (BD Biosciences, Cat# 349202), washed, and analyzed via FC. .. Materials and reagents with respective vendors were as follows: from Miltenyi Biotec, CD3-VioBlue (Cat# 130-113-133; RRID: AB_10831672), CD19-APC (Cat# 130-113-165; RRID: AB_2725993), and running buffer (Cat# 130-091-221); from Sony Biotechnology, CD4-PE/Cy7 (Cat# 2387050), CD8-FITC (Cat# 2323520), CD123-PE/Cy7 (Cat# 2130050), 7-AAD Viability Staining Solution (Cat# 2702020), CD45-Brilliant Violet 510 (Cat# 2120180), CD45-APC (Cat# 1338540), CD19-APC (Cat# 2111060), CD14APC/Cy7 (Cat# 2435540), CD303-FITC (Cat# 2371040), and CD19PE (Cat# 2111040); from Invitrogen, Monensin Solution (Cat# 00- 4505-51) and eBioscience Cell Proliferation Dye eFluor 450 (Cat# 65-0863); from BD Pharmingen, CD33-PE (Cat# 345799; RRID: AB_2868826), HLA-DR-PerCP-Cy5.5 (Cat# 560652; RRID: AB_1727529), CD34-APC (Cat# 555824; RRID: AB_398614), CD38-APC-H7 (Cat# 656646; RRID: AB_2870413), CD107a-FITC OF2 Cancer Immunol Res; 2024 CANCER IMMUNOLOGY RESEARCH Fredon et al. D ow nloaded from http://aacrjournals.org/cancerim m unolres/article-pdf/doi/10.1158/2326-6066.C IR -23-0548/3463330/cir-23-0548.pdf by IN SER M user on 20 June 2024 (Cat# 555800; RRID: AB_396134), and Streptavidin-APC (Cat# 554067; RRID AB_10050396); from BD Biosciences, Trucount Absolute Counting Tubes IVD (Cat# 663028); and from R&D Systems, recombinant human IL3R alpha/CD123 protein (Cat# 301-R2-025). .. Determination of the absolute number of CD123 antigenic sites on Gen2.2, CAL1, MA-9-RAS, HMEC1, and Daudi cell lines as well as on primary CD34+ and CD14+ cells was done using indirect immunofluorescence FC using Mouse IgG Calibrator (BioCytex, Cat# CP051).

    other:

    Article Title: A novel label-free method to determine equilibrium dissociation constants of antibodies binding to cell surface proteins.
    Article Snippet: To detect free (unbound) antibody in solution using the (ECLIA) assay, MSD SA-STD plates were blocked with 50 μL per well of assay buffer (PBS containing 0.2% BSA, 0.05% Tween 20) for at least 5 min. Plates were turned over to remove assay buffer and tapped on paper towels and 50 μL per well of 0.7 μg/mL biotinylated human CD123 SP1 (huCD123 SP1, R&D Systems cat 301-R3/CF, lot# LV091112A or LV081110A) or human CD123 SP2 BlueSky Lot #120,503-CP05057h or 6519A) in assay buffer were added and the plates were allowed to incubate overnight in the refrigerator.



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    Image Search Results


    Representative SPR sensorgrams obtained by Biacore of antibody mAb I3RB18 Fab (I3RB119), and BsAbs binding to recombinant human antigen CD123 SP1 ( A ) and its truncated variant CD123 SP2 ( B ).

    Journal: Scientific Reports

    Article Title: A novel label-free method to determine equilibrium dissociation constants of antibodies binding to cell surface proteins

    doi: 10.1038/s41598-024-82288-9

    Figure Lengend Snippet: Representative SPR sensorgrams obtained by Biacore of antibody mAb I3RB18 Fab (I3RB119), and BsAbs binding to recombinant human antigen CD123 SP1 ( A ) and its truncated variant CD123 SP2 ( B ).

    Article Snippet: To detect free (unbound) antibody in solution using the (ECLIA) assay, MSD SA-STD plates were blocked with 50 μL per well of assay buffer (PBS containing 0.2% BSA, 0.05% Tween 20) for at least 5 min. Plates were turned over to remove assay buffer and tapped on paper towels and 50 μL per well of 0.7 μg/mL biotinylated human CD123 SP1 (huCD123 SP1, R&D Systems cat 301-R3/CF, lot# LV091112A or LV081110A) or human CD123 SP2 BlueSky Lot #120,503-CP05057h or 6519A) in assay buffer were added and the plates were allowed to incubate overnight in the refrigerator.

    Techniques: Binding Assay, Recombinant, Variant Assay

    Biacore and MSD-CAT affinity data for the binding of  anti-CD123  to human antigen-full length (CD123 SP1) and its truncated variant (CD123 SP2). For the SPR experiment recombinant CD123 SP1 or CD123 SP2 were used for complex formation. For the MSD-CAT experiments reported in the last column, complex formation was obtained by incubating antibodies or Fabs with cells expressing human CD123 SP1 or CD123 SP2, or cynomolgus full length CD123. Detection of antibody in the cell-antibody equilibrated mixture was performed by capturing free antibody in the supernatant with biotinylated recombinant CD123 SP1 or CD123 SP2 which has been previously captured on a streptavidin MSD-plate.

    Journal: Scientific Reports

    Article Title: A novel label-free method to determine equilibrium dissociation constants of antibodies binding to cell surface proteins

    doi: 10.1038/s41598-024-82288-9

    Figure Lengend Snippet: Biacore and MSD-CAT affinity data for the binding of anti-CD123 to human antigen-full length (CD123 SP1) and its truncated variant (CD123 SP2). For the SPR experiment recombinant CD123 SP1 or CD123 SP2 were used for complex formation. For the MSD-CAT experiments reported in the last column, complex formation was obtained by incubating antibodies or Fabs with cells expressing human CD123 SP1 or CD123 SP2, or cynomolgus full length CD123. Detection of antibody in the cell-antibody equilibrated mixture was performed by capturing free antibody in the supernatant with biotinylated recombinant CD123 SP1 or CD123 SP2 which has been previously captured on a streptavidin MSD-plate.

    Article Snippet: To detect free (unbound) antibody in solution using the (ECLIA) assay, MSD SA-STD plates were blocked with 50 μL per well of assay buffer (PBS containing 0.2% BSA, 0.05% Tween 20) for at least 5 min. Plates were turned over to remove assay buffer and tapped on paper towels and 50 μL per well of 0.7 μg/mL biotinylated human CD123 SP1 (huCD123 SP1, R&D Systems cat 301-R3/CF, lot# LV091112A or LV081110A) or human CD123 SP2 BlueSky Lot #120,503-CP05057h or 6519A) in assay buffer were added and the plates were allowed to incubate overnight in the refrigerator.

    Techniques: Binding Assay, Variant Assay, Recombinant, Expressing

    Representative binding curves for MSD-CAT affinity analysis for cell surface expressed CD123, SP1 ( A ) and CD123 SP2 ( B ). The Y-axis shows % free anti-receptor molecules (BsAb, Fab or mAb) or CD123 negative control mAb (I3CB15) while the X-axis shows the concentration of cell surface antigen. Each curve represents a different but fixed concentration of mAb, bispecific or Fab as indicated.

    Journal: Scientific Reports

    Article Title: A novel label-free method to determine equilibrium dissociation constants of antibodies binding to cell surface proteins

    doi: 10.1038/s41598-024-82288-9

    Figure Lengend Snippet: Representative binding curves for MSD-CAT affinity analysis for cell surface expressed CD123, SP1 ( A ) and CD123 SP2 ( B ). The Y-axis shows % free anti-receptor molecules (BsAb, Fab or mAb) or CD123 negative control mAb (I3CB15) while the X-axis shows the concentration of cell surface antigen. Each curve represents a different but fixed concentration of mAb, bispecific or Fab as indicated.

    Article Snippet: To detect free (unbound) antibody in solution using the (ECLIA) assay, MSD SA-STD plates were blocked with 50 μL per well of assay buffer (PBS containing 0.2% BSA, 0.05% Tween 20) for at least 5 min. Plates were turned over to remove assay buffer and tapped on paper towels and 50 μL per well of 0.7 μg/mL biotinylated human CD123 SP1 (huCD123 SP1, R&D Systems cat 301-R3/CF, lot# LV091112A or LV081110A) or human CD123 SP2 BlueSky Lot #120,503-CP05057h or 6519A) in assay buffer were added and the plates were allowed to incubate overnight in the refrigerator.

    Techniques: Binding Assay, Negative Control, Concentration Assay

    Binding curves for MSD-CAT affinity analysis for cyno CD123. The Y-axis shows % free anti-receptor molecules (mAb or its Fab) while the X-axis shows the concentration of cell surface antigen. Each curve represents a different but fixed concentration of mAb, or Fab as indicated. The figure also shows a plot of the control commercial antibody, 7G3, showing cross reactivity to human CD123 (SP1).

    Journal: Scientific Reports

    Article Title: A novel label-free method to determine equilibrium dissociation constants of antibodies binding to cell surface proteins

    doi: 10.1038/s41598-024-82288-9

    Figure Lengend Snippet: Binding curves for MSD-CAT affinity analysis for cyno CD123. The Y-axis shows % free anti-receptor molecules (mAb or its Fab) while the X-axis shows the concentration of cell surface antigen. Each curve represents a different but fixed concentration of mAb, or Fab as indicated. The figure also shows a plot of the control commercial antibody, 7G3, showing cross reactivity to human CD123 (SP1).

    Article Snippet: To detect free (unbound) antibody in solution using the (ECLIA) assay, MSD SA-STD plates were blocked with 50 μL per well of assay buffer (PBS containing 0.2% BSA, 0.05% Tween 20) for at least 5 min. Plates were turned over to remove assay buffer and tapped on paper towels and 50 μL per well of 0.7 μg/mL biotinylated human CD123 SP1 (huCD123 SP1, R&D Systems cat 301-R3/CF, lot# LV091112A or LV081110A) or human CD123 SP2 BlueSky Lot #120,503-CP05057h or 6519A) in assay buffer were added and the plates were allowed to incubate overnight in the refrigerator.

    Techniques: Binding Assay, Concentration Assay, Control

    Representative SPR sensorgrams obtained by Biacore of antibody mAb I3RB18 Fab (I3RB119), and BsAbs binding to recombinant human antigen CD123 SP1 ( A ) and its truncated variant CD123 SP2 ( B ).

    Journal: Scientific Reports

    Article Title: A novel label-free method to determine equilibrium dissociation constants of antibodies binding to cell surface proteins

    doi: 10.1038/s41598-024-82288-9

    Figure Lengend Snippet: Representative SPR sensorgrams obtained by Biacore of antibody mAb I3RB18 Fab (I3RB119), and BsAbs binding to recombinant human antigen CD123 SP1 ( A ) and its truncated variant CD123 SP2 ( B ).

    Article Snippet: For generation of monoclonal anti-CD123 antibodies, recombinant human CD123 SP1 ECD-His tag protein (R&D Systems, 301-R3/CF, lot# LV081110A) was used for phage panning and hit screening.

    Techniques: Binding Assay, Recombinant, Variant Assay

    Biacore and MSD-CAT affinity data for the binding of  anti-CD123  to human antigen-full length (CD123 SP1) and its truncated variant (CD123 SP2). For the SPR experiment recombinant CD123 SP1 or CD123 SP2 were used for complex formation. For the MSD-CAT experiments reported in the last column, complex formation was obtained by incubating antibodies or Fabs with cells expressing human CD123 SP1 or CD123 SP2, or cynomolgus full length CD123. Detection of antibody in the cell-antibody equilibrated mixture was performed by capturing free antibody in the supernatant with biotinylated recombinant CD123 SP1 or CD123 SP2 which has been previously captured on a streptavidin MSD-plate.

    Journal: Scientific Reports

    Article Title: A novel label-free method to determine equilibrium dissociation constants of antibodies binding to cell surface proteins

    doi: 10.1038/s41598-024-82288-9

    Figure Lengend Snippet: Biacore and MSD-CAT affinity data for the binding of anti-CD123 to human antigen-full length (CD123 SP1) and its truncated variant (CD123 SP2). For the SPR experiment recombinant CD123 SP1 or CD123 SP2 were used for complex formation. For the MSD-CAT experiments reported in the last column, complex formation was obtained by incubating antibodies or Fabs with cells expressing human CD123 SP1 or CD123 SP2, or cynomolgus full length CD123. Detection of antibody in the cell-antibody equilibrated mixture was performed by capturing free antibody in the supernatant with biotinylated recombinant CD123 SP1 or CD123 SP2 which has been previously captured on a streptavidin MSD-plate.

    Article Snippet: For generation of monoclonal anti-CD123 antibodies, recombinant human CD123 SP1 ECD-His tag protein (R&D Systems, 301-R3/CF, lot# LV081110A) was used for phage panning and hit screening.

    Techniques: Binding Assay, Variant Assay, Recombinant, Expressing

    Representative binding curves for MSD-CAT affinity analysis for cell surface expressed CD123, SP1 ( A ) and CD123 SP2 ( B ). The Y-axis shows % free anti-receptor molecules (BsAb, Fab or mAb) or CD123 negative control mAb (I3CB15) while the X-axis shows the concentration of cell surface antigen. Each curve represents a different but fixed concentration of mAb, bispecific or Fab as indicated.

    Journal: Scientific Reports

    Article Title: A novel label-free method to determine equilibrium dissociation constants of antibodies binding to cell surface proteins

    doi: 10.1038/s41598-024-82288-9

    Figure Lengend Snippet: Representative binding curves for MSD-CAT affinity analysis for cell surface expressed CD123, SP1 ( A ) and CD123 SP2 ( B ). The Y-axis shows % free anti-receptor molecules (BsAb, Fab or mAb) or CD123 negative control mAb (I3CB15) while the X-axis shows the concentration of cell surface antigen. Each curve represents a different but fixed concentration of mAb, bispecific or Fab as indicated.

    Article Snippet: For generation of monoclonal anti-CD123 antibodies, recombinant human CD123 SP1 ECD-His tag protein (R&D Systems, 301-R3/CF, lot# LV081110A) was used for phage panning and hit screening.

    Techniques: Binding Assay, Negative Control, Concentration Assay

    Binding curves for MSD-CAT affinity analysis for cyno CD123. The Y-axis shows % free anti-receptor molecules (mAb or its Fab) while the X-axis shows the concentration of cell surface antigen. Each curve represents a different but fixed concentration of mAb, or Fab as indicated. The figure also shows a plot of the control commercial antibody, 7G3, showing cross reactivity to human CD123 (SP1).

    Journal: Scientific Reports

    Article Title: A novel label-free method to determine equilibrium dissociation constants of antibodies binding to cell surface proteins

    doi: 10.1038/s41598-024-82288-9

    Figure Lengend Snippet: Binding curves for MSD-CAT affinity analysis for cyno CD123. The Y-axis shows % free anti-receptor molecules (mAb or its Fab) while the X-axis shows the concentration of cell surface antigen. Each curve represents a different but fixed concentration of mAb, or Fab as indicated. The figure also shows a plot of the control commercial antibody, 7G3, showing cross reactivity to human CD123 (SP1).

    Article Snippet: For generation of monoclonal anti-CD123 antibodies, recombinant human CD123 SP1 ECD-His tag protein (R&D Systems, 301-R3/CF, lot# LV081110A) was used for phage panning and hit screening.

    Techniques: Binding Assay, Concentration Assay, Control