Overview

is a laboratory centrifuge designed for quick and efficient microcentrifugation. It is widely used in molecular biology, biochemistry, and clinical research for various applications such as cell separation, nucleic acid purification, and protein precipitation. The microfuge offers high centrifugal force, compact design, and user-friendly features, making it a valuable tool in research laboratories.

Features and Specifications

  • High Centrifugal Force: offers maximum centrifugal force ranging from 12,000 to 21,000 x g, depending on the rotor type.
  • Compact Design: The microfuge has a compact footprint, making it ideal for space-constrained laboratories.
  • Easy-to-Use: It features an intuitive control panel with digital display for precise speed and time setting.
  • Versatile Rotors: Various rotors are available to accommodate different sample types and volumes, including fixed-angle, swinging-bucket, and microplate rotors.
  • Quick Acceleration and Deceleration: The microfuge accelerates and decelerates quickly, minimizing processing time.
  • Safety Features: It is equipped with safety features such as an automatic lid lock and imbalance detection to ensure safe operation.

Applications

is widely used in various applications, including:

  • Cell Separation: Separating cells, organelles, and other particles based on size and density.
  • Nucleic Acid Purification: Removing impurities and contaminants from DNA and RNA samples.
  • Protein Precipitation: Pelleting proteins out of solution for analysis or purification.
  • Immunoassays: Performing agglutination and precipitation reactions for immunological studies.
  • Clinical Diagnostics: Centrifuging blood samples for hematology and serum analysis.

Advantages

  • High centrifugal force for efficient separation and precipitation.
  • Compact design for space-saving in the laboratory.
  • Easy-to-use interface for quick and accurate operation.
  • Versatile rotors for accommodating different sample formats.
  • Quick acceleration and deceleration for time-efficient processing.
  • Safety features for safe and reliable operation.

Comparison with Other Microfuges

Feature Other Microfuges
Centrifugal Force 12,000 – 21,000 x g 10,000 – 15,000 x g
Rotor Versatility Fixed-angle, swinging-bucket, microplate Limited rotor options
User Interface Intuitive digital display Basic analog controls
Safety Features Automatic lid lock, imbalance detection May not have all safety features
Footprint Compact May be bulkier

Frequently Asked Questions (FAQs)

Q: What is the maximum centrifugal force of the ?
A: The maximum centrifugal force varies depending on the rotor used, ranging from 12,000 to 21,000 x g.

Q: How many rotors are available for the microfuge?
A: A variety of rotors are available, including fixed-angle, swinging-bucket, and microplate rotors.

Q: Is the microfuge easy to use?
A: Yes, it features an intuitive control panel with a digital display for precise speed and time setting.

Q: What safety features does the microfuge have?
A: It has safety features such as an automatic lid lock and imbalance detection to ensure safe operation.

Q: What types of applications can the microfuge be used for?
A: It is widely used for cell separation, nucleic acid purification, protein precipitation, immunoassays, and clinical diagnostics.

Conclusion

is a versatile and reliable laboratory centrifuge that meets the demands of various research and clinical applications. Its high centrifugal force, compact design, user-friendly features, and safety measures make it a valuable asset in any laboratory.

References

Monoclonal Antibody Production Kit

This kit provides a comprehensive solution for the rapid and efficient production of monoclonal antibodies (mAbs). Key features include:

  • Hybridoma Fusion: Facilitates fusion between B cells and myeloma cells to generate hybridoma cells producing specific mAbs.
  • Hybridoma Selection: Selective media and cloning techniques allow identification and isolation of hybridoma cells producing high-affinity mAbs.
  • Antibody Characterization: ELISA and flow cytometry analysis tools enable determination of mAb specificity, affinity, and isotype.
  • Antibody Production: Hybridoma cells are scaled up and cultured for bulk production of purified mAbs.
  • Quality Control: Stringent testing protocols assess mAb purity, potency, and specificity.
  • Rapid and Efficient: Streamlined workflow minimizes production time and maximizes antibody yield.

Monoclonal Antibody Cloning Techniques

Monoclonal antibodies (mAbs) are antibodies produced by identical immune cells, targeting a specific antigen. To generate mAbs, various cloning techniques are employed:

Hybridoma Technology:

  • Fuses antibody-producing B cells with myeloma cells, creating hybridomas that secrete mAbs indefinitely.
  • Mice immunized with the antigen of interest provide the B cells.

Single-Cell Cloning:

  • Separates individual B cells from hybridoma colonies.
  • Grows each B cell into a clonal population of identical antibody-producing cells.
  • Ensures the production of mAbs that recognize a single epitope.

Recombinant DNA Technology:

  • Isolates the gene encoding the antibody molecule from the hybridoma or B cell.
  • Injects the gene into a host cell, such as Chinese Hamster Ovary (CHO) cells, enabling large-scale mAb production.

Phage Display Technology:

  • Inserts antibody genes into the genome of bacteriophages.
  • Selects and amplifies phages displaying mAbs with the desired specificity.
  • Allows for rapid screening and optimization of mAb candidates.

Cell Line Engineering:

  • Modifies existing cell lines, such as CHO cells, to enhance mAb production and quality.
  • Introduces genes encoding transcription factors or post-translational modifiers to improve antibody expression and folding.

Monoclonal Antibody Biology and Applications

Monoclonal antibodies (mAbs) are highly specific immune proteins that bind to a single epitope on an antigen. They are produced by hybridomas, which are created by fusing a B cell with a tumor cell. mAbs have several advantages over traditional polyclonal antibodies, including:

  • High specificity: mAbs bind to a single epitope on an antigen, making them highly specific for their target.
  • Reproducibility: mAbs can be produced in large quantities in a highly reproducible manner, making them ideal for research and therapeutic applications.
  • Versatility: mAbs can be used for a wide variety of applications, including:
    • Research: mAbs can be used to identify and characterize proteins, study protein-protein interactions, and develop diagnostic assays.
    • Therapy: mAbs can be used to treat a variety of diseases, including cancer, autoimmune disorders, and infectious diseases.
    • Imaging: mAbs can be used to visualize the distribution and expression of proteins in vivo.

Monoclonal Antibody Cloning Protocols

Monoclonal antibodies are produced by hybridomas, which are cells that are formed by the fusion of a myeloma cell with a B cell. Myeloma cells are cancer cells that produce antibodies, while B cells are white blood cells that produce antibodies against specific antigens. Hybridomas are immortal cells that can produce monoclonal antibodies indefinitely.

There are a number of different protocols for cloning monoclonal antibodies. One common protocol is the following:

  1. Immunize a mouse with the antigen of interest.
  2. Collect the mouse’s splenocytes (spleen cells).
  3. Fuse the splenocytes with myeloma cells.
  4. Select hybridomas that are producing the desired antibody.
  5. Clone the hybridomas by limiting dilution.
  6. Characterize the monoclonal antibodies.

This protocol can be used to produce monoclonal antibodies against any antigen. The antibodies can be used for a variety of applications, including research, diagnostics, and therapeutics.

Monoclonal Antibody Cloning Troubleshooting

Common Issues and Solutions

  • Low cloning efficiency: Optimize culture conditions, adjust selection stringency, or use a more sensitive reporter system.
  • No distinguishable clones: Ensure proper cell separation, optimize dilution, or use a brighter reporter signal.
  • Non-specific binding: Assess reagent and antibody specificity, optimize washing conditions, or use a blocking agent.
  • Clonal instability: Determine the cause (e.g., genetic drift, contamination), maintain optimal culture conditions, or select clones with stable expression.
  • Poor antibody expression: Check for proper gene integration, optimize culture conditions, or use a more efficient expression vector.
  • Cross-reactivity: Test antibody specificity with multiple targets, use negative controls, or perform competitive binding assays.
  • Batch-to-batch variation: Ensure consistent production processes, maintain stable cell lines, or use a standardized batch production method.
  • Contamination: Perform sterility testing, ensure aseptic techniques, or use antibiotics and antimycotics.
  • Poor antibody functionality: Optimize assay conditions, assess antibody stability, or use a different antibody isotype or format.
  • Non-specific effects: Use appropriate controls, optimize reagent concentrations, or perform blocking experiments.

Monoclonal Antibody Cloning Cost

The cost of cloning monoclonal antibodies can vary depending on various factors, including:

  • Source of the antibodies: Hybridomas or cell lines may have different costs for development and maintenance.
  • Size of the project: The number of antibodies to be cloned affects the overall cost.
  • Complexity of the cloning process: Cloning antibodies with specific characteristics or modifications may require specialized techniques.
  • Reagents and materials: The cost of cell culture media, reagents, and consumables can add up.
  • Expertise and labor: The experience and skill of the personnel involved in cloning can impact the cost.

Estimated costs can range from a few thousand dollars to tens of thousands of dollars per antibody, depending on the specific requirements. It is recommended to contact specialized laboratories or contract research organizations for accurate pricing information based on your project’s specifications.

Monoclonal Antibody Cloning Services

Monoclonal antibody cloning services provide expertise in isolating, developing, and producing highly specific antibodies for research, diagnostic, and therapeutic applications. These services offer advanced techniques such as hybridoma technology, recombinant antibody expression, and cell line optimization to create custom monoclonal antibodies tailored to meet specific experimental or clinical requirements.

Cloning services provide a valuable resource for researchers and clinicians by:

  • Generating high-affinity antibodies: They isolate and select antibodies with exceptional binding specificity and affinity towards target antigens.
  • Developing antibodies for various applications: Services cater to diverse needs, including research tools, diagnostic assays, and therapeutic agents.
  • Offering technical expertise: Specialized teams provide guidance and expertise in antibody development, purification, and characterization.
  • Ensuring consistent quality: Cloning services adhere to strict quality control measures to ensure the consistency and reproducibility of antibodies produced.

Beckman Coulter Centrifuge for Monoclonal Antibody Cloning

The Beckman Coulter centrifuge is a specialized laboratory equipment used for the isolation and purification of monoclonal antibodies (mAbs) in the process of monoclonal antibody cloning.

Key Features:

  • High Speed: Capable of reaching speeds up to 100,000 x g, enabling efficient separation of mAbs from cell debris and other impurities.
  • High Capacity: Accommodates a range of rotor sizes, allowing for the processing of large volumes of cell culture supernatant or other samples.
  • Automated Operation: Features programmable control systems for precise temperature, speed, and run time, ensuring reproducibility and standardization.

Applications:

The Beckman Coulter centrifuge plays a crucial role in the purification and isolation of mAbs during monoclonal antibody cloning. It enables researchers to:

  • Separate mAbs from impurities: Remove cell debris, protein aggregates, and other contaminants to obtain highly purified mAbs.
  • Concentrate mAbs: Increase the concentration of mAbs for downstream applications, such as characterization and production.
  • Isolate specific mAbs: Utilize specialized rotors and protocols to selectively isolate specific mAbs based on their size, charge, or other properties.
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