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Purification Techniques | Boost Antibody Purification ——BioLink MaXtar® Protein L Application Cases

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    In the R&D and production process of antibody drugs, an efficient and stable purification process is a key link to ensure product quality and production efficiency. Since BioLink antibody affinity resin MaXtar® Protein L launches, Protein L has become an important tool for the purification of various antibody fragments (such as Fab, scFv, Dab, etc.) and intact antibodies (such as IgG, IgM and bispecific antibodies) by virtue of its specific binding to kappa light chain variable region.


    figure-1-structural-form-of-protein-l-binding-to-molecules.jpg

    Figure 1: Structural form of Protein L binding to molecules


    Core Competencies of MaXtar® Protein L Resin

    • Highly cross-linked agarose-based matrix for improved process efficiency.

    • Stronger alkali resistance, low ligand shedding, prolonged service life.

    • Stable batch-to-batch consistency.

    • Protein L ligand protected by intellectual property rights, perfect regulatory support files (RSF).

    • 200 L single batch production capacity up to 200 L, short delivery time, stable supply chain, and high cost performance.


    Product Parameters

    Manufacturer

    BioLink

    Resin

    MaXtar® Protein L

    Matrix

    Highly Cross-Linked Agarose

    Ligand

    rProtein L

    Average Particle Size

    65μm

    Dynamic Binding Capacity

    ≥50 mg IgG1/mL(RT 6min)

    Maximum Pressure Resistance

    0.5 MPa

    CIP

    0.05~0.1M NaoH

    pH Stability

    3~12 (Long-Term)

    2~13 (Short-Term)

    Storage Conditions

    20% Ethanol, 2~8℃

    *Binding capacity depends on the specificity of the antibody molecule

    Table 1: MaXtar® Protein L product parameters


    Stable Batch-to-batch Consistency


    figure-2-the-dynamic-binding-capacity-rsd.jpg

    Figure 2: The dynamic binding capacity RSD of 3 batches is < 5%, and the consistency between batches is relatively stable.


    Application Case Sharing —— Fab Purification

    • Column: Chrom-LinX® 16 mm * 18 cm

    • CV: 36 mL

    Step

    Buffer

    CV

    Residence Time
    (min)

    Sanitization

    0.05 mol/L NaOH

    3.0

    5

    Equilibration

    25 mM Tris,0.15 M NaCl,pH 7.4

    3.0

    5

    Sample Loading

    Fab Cell Supernatant

    Loading at 27 mg/mL

    5

    Re-equilibration

    25 mM Tris,0.15 M NaCl,pH 7.4

    5.0

    5

    Wash I

    50 mM NaAC-HAc,1M NaCl,pH 5.5

    3.0

    5

    Wash II

    50 mM NaAC-HAc,pH 5.5

    3.0

    5

    Elution

    50 mM NaAC-HAc,pH 3.0

    5.0

    5

    Post-sanitization

    0.05mol/L NaOH

    3.0

    5

    Storage

    20% Ethanol

    2.0

    5

    Table 2: Process Conditions



    figure-3-maxtar-protein-l-purified-fab-fragments.jpg

    Figure 3: MaXtar® Protein L purified Fab fragments


    CAT. NO.

    Resin

    Yield A(%)

    SEC(%)

    Collected CV

    MaXtar® Protein L

    88

    99

    1.5

    Table 3: MaXtar® Protein L purification data


    Summary: After purification of MaXtar® Protein L, the purity and recovery performance are in line with expectations, and it still has good elution performance under sodium acetate system.


    References

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