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Veterinary Therapeutic Antibody Hybridoma Platform

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Antigen Preparation Animal Immunization Cell Fusion Hybridoma Cell Screening Monoclonal Antibody Production Antibody Engineering Why Choose Us?

Hybridoma cell lines are created by fusing antigen-activated B cells from mice with myeloma cells. These hybridoma cells undergo screening to identify those capable of secreting monoclonal antibodies targeting a specific antigenic determinant. BioVenic has developed a robust hybridoma platform, enabling the efficient production of veterinary monoclonal antibodies with exceptional specificity. From the initial antigen preparation to the subsequent animal immunization, and through the rigorous screening and identification process, we are dedicated to meeting and exceeding expectations.

Fig.1. Monoclonal antibody production: A hybridoma technology approach. (Saeed, Abdullah FUH, et al., 2017)Fig.1 Process for the preparation of monoclonal antibodies using a hybridoma technology platform.1,2

Antigen Preparation

BioVenic provides various types of antigen preparation services to meet requirements. The higher antigen purity used to prepare the monoclonal antibody, the higher the success rate of the monoclonal antibody preparation.

Proteins Peptides DNA mRNA VLP

Animal Immunization

Animal immunization is no one-size-fits-all approach, BioVenic conducts a thorough analysis of the characteristics of target antigens. We consider various factors such as the nature of the antigen, the immunization route, and its immunogenicity to tailor a personalized animal immunization plan. Here are the adjustment items of the animal immunization protocol.

Antigen Dosage Immunization Frequency Adjuvant Use

Cell Fusion

BioVenic provides PEG fusion services, ensuring excellent fusion results by rigorously controlling the concentration, molecular weight, and exposure time of PEG to samples. BioVenic also offers electrofusion services. We have introduced advanced electrofusion equipment, and key factors for successful electrofusion, such as electric field strength, pulse number, and pulse duration, all adjusted within a range by our professionals.

PEG Fusion

Polyethylene glycol (PEG) can lead to cellular dehydration and changes in cell membrane structure, resulting in the fusion of myeloma cells and mouse B lymphocytes. This substance is easy to prepare, stable in nature, and convenient to use.

Electrofusion

As a physical method, electrofusion technology offers high fusion efficiency, low cell toxicity, and the absence of chemical substances and viruses. It utilizes an electric field to connect cells in series, followed by the application of momentary high-voltage pulses to induce reversible electroporation of the cell membranes, thereby promoting cell fusion.

Hybridoma Cell Screening

Various fusion outcomes are generated after fusion, including unfused cells, self-fused cells, and correctly fused hybridoma cells. BioVenic provides hybridoma cell screening services to obtain the correct cells. We utilize HAT medium, which contains hypoxanthine, aminopterin, and thymidine, for cell screening, only the fused hybridoma cells can proliferate indefinitely in HAT medium. Our professional staff used limiting dilution analysis to serially dilute the hybridoma cells. We test whether the antibodies secreted by the cells in the supernatant of each well can bind to specific antigens. This process is repeated multiple times until it ensures that each well's proliferating cells are monoclonal.

Monoclonal Antibody Production

Using hybridoma cell technology to produce monoclonal antibodies for veterinary use, BioVenic offers two primary methods, ascites production and in vitro culturing. Our expertise in these methods ensures that clients receive high-quality, specific monoclonal antibodies for their development projects.

Ascites Production

Hybridoma cells are implanted into the peritoneal cavity of mice, leading to ascites production containing substantial amounts of monoclonal antibodies. This approach enables the rapid generation of a large quantity of veterinary monoclonal antibodies. BioVenic provides a high-quality animal housing environment and skilled personnel to ensure animal welfare.

In Vitro Culturing

In vitro culturing involves culturing selected hybridoma cells in a suitable growth medium. BioVenic has introduced high-capacity bioreactors capable of high-density culturing of hybridoma cells. Additionally, we offer cell conditioning services using low or serum-free culture media to reduce impurities in the final product, while also addressing concerns related to animal-derived contamination and animal welfare.

Antibody Engineering

Mouse-derived antibodies used in target animals such as canine and feline may exhibit significant heterogeneity. This may not only lead to suboptimal therapeutic efficacy but may also pose safety concerns. BioVenic offers antibody caninization and felinization services to reduce antibody immunogenicity. We also offer affinity maturation services to maintain potentially reduced antibody affinity.

Why Choose Us?

A one-stop veterinary therapeutic antibody development service utilizing hybridoma technology for a more convenient experience.

Provides highly specific antibody production services to ensure consistent affinity and specificity.

Customized design and optimization of antibodies according to specific needs.

Hybridoma technology, as one of the classic methods for veterinary monoclonal antibody development, has been successfully applied in numerous projects. BioVenic has established the veterinary therapeutic antibody hybridoma platform to provide services for developing high-quality veterinary therapeutic antibodies using hybridoma technology. If you have such needs, please don't hesitate to contact us!

References

  1. Saeed, Abdullah FUH, et al. "Antibody engineering for pursuing a healthier future." Frontiers in microbiology (2017): 495.
  2. Image retrieved from Figure 2 "Illustration showing the production route of hybridoma technology.", Saeed, Abdullah FUH, et al., 2017, used under [CC BY 4.0], the image title was changed to "Process for the preparation of monoclonal antibodies using a hybridoma technology platform."
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