Mouse monoclonal antibody has many features such as targeting to a single epitope, high specificity, stable passage, large-scale manufacturing and extensive applications in basic research, medical diagnosis, tumor therapy and radioimmunoimaging. With hybridoma technology, Sino Biological has developed mouse monoclonal antibodies (mAbs), which have advantages of high sensitivity and specificity. We can also provide flexible customized solutions according to customer requirements, aiming to provide customers with high-quality antibodies.
Service procedures | Specification | Timeline | Deliverables | Guarantee | Price |
---|---|---|---|---|---|
① Antigen preparationQuote! |
Please refer to antigen production service | ||||
② Antigen validation |
• Analysis of client's antigen by SDS-PAGE and UV | 1-2 days | • 2-5 strains of ELISA positive clones (2 tubes of cryopreserved cells) • 2-5mL supernatant per clone • 1-3mg purified antibody (choose a hybridoma cell) • Experimental report |
ELISA positive for immunogen | |
③ Immunization and serum titer test |
• Pre-immune bleed • Five Balb/c mice immunization • Serum titer test • Final bleed |
8-10 weeks | |||
④ Fusion and Screening |
• Fusion and Screening • Subcloning and cell expansion • Cell Banking |
4-6 weeks | |||
⑤ Antibody production & purification |
• Appropriate scale hybridoma cell culture • Purified by protein A affinity chromatography |
2-3 weeks | |||
⑥ QC analysis |
• Analysis by SDS-PAGE and UV • ELISA validation |
3 days |
Recombinant protein antigen | Peptide antigen | ||
---|---|---|---|
Antigen quantities | 3-4mg/5 mice | • KLH/VLP conjugated peptides | 5mg/5 mice |
Antigen Size | >10kD | Concentration | >0.5mg/mL |
SDS-Page purity | >90% | • OVA/Biotin conjugated peptides | 2-3mg |
Concentration | >0.5mg/mL | Concentration | >0.1mg/mL |
Formulation | PBS, if not PBS, please inquire first | Formulation | PBS, if not PBS, please inquire first |
Sino Biological Inc. has established a high-throughput mouse monoclonal antibody R&D platform. A set of high-throughput R&D programs for mouse monoclonal antibodies are also established through the optimization of immunization protocols, fusion protocols, screening protocols, and high-throughput antibody production and purification protocols. All of our mouse mAbs are validated by ELISA, WB, IHC, FACS et al. , and are tested by multi-tissue and multi-cell.
a)Multi-cell, multi-tissue validation
• Human placenta |
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Fig 1. Immunochemical staining of human target D with mouse Mab. The left panel: tissue incubated with primary antibody; The right panel: tissue incubated with the mixture of primary antibody and antigen. |
• Human breast carcinoma |
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Fig 2. Immunochemical staining of human target D with mouse monoclonal antibody. |
b)Multi-application verification
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Fig 1. Confocal immunofluorescence analysis of human target D in MCF7 cells. Positive staining was localized to lysosome membrane. |
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Fig 2. Flow cytometric analysis of human target D on Jurkat cells. The histogram were derived from gated events with the forward and side light-scatter characteristics of intact cells. |
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Fig 3. Lane A: Jurkat Whole Cell Lysate. Anti-target D mouse Mab; goat Anti-mouse IgG H&L (Dylight800). |
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Fig 4. Lane A: Hela Whole Cell Lysate; Lane B: Jurkat Whole Cell Lysate; Lane C: Daudi Whole Cell Lysate. Anti-target D mouse Mab; Dylight 800-labeled antibody to Mouse IgG (H+L). |