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Cellectra™ Human CD8 NanoSort Microbeads, Research grade

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Product Number/Spec
Price
Menge
MBS-S005-2ml
$513.00
ETA of in-stock products:2 business days
Gesamtanzahl Product Amount$ 0

Product Details

  • Product
    Size
    Amount
    Cellectra™ Human CD8 NanoSort Microbeads, Research grade
    2 mL
    For 10⁹ total cells
  • Product Show

    CD8 PRODUCT SHOW

    This product is compatible with mainstream automated cell processing instruments and commercially available column-based (M/D/L) magnetic separation systems.

  • Features

    1. High Safety
      1. Raw Material Safety: The conjugated antibodies are recombinant antibodies, avoiding contamination from animal-derived viruses and exogenous factor pollutants. Medical-grade nanoparticles with dextran matrix coating - high biocompatibility, biodegradable.
      2. Supply Chain Safety: Highly integrated autonomous platforms for nano-magnetic beads and single B-cell antibody.
      3. Process Safety : AOF production process prevents exogenous factor contamination, with rigorous quality control ensuring product safety.
    2. High Sorting Purity
      1. Conjugated antibodies are derived from a single B-cell antibody development platform, featuring optimized antibody epitopes.
      2. Nanoscale superparamagnetic beads enable efficient and gentle cell sorting.
    3. Long-Term Stability
      1. Stable for 24 months at -20 °C or below.
  • Product Description

    Cellectra™ Human CD8 NanoSort Microbeads are dextran-coated superparamagnetic nanoparticles conjugated with recombinant monoclonal antibodies specific to human CD8. They are especially designed for positive or negative selection of CD8+ cells.
    The beads are manufactured under sterile ISO 5 conditions with no animal- or human-derived components. Each batch undergoes rigorous quality control, including sterility, endotoxin, and functional validation.

  • Application

    Cellectra™ Human CD8 NanoSort Microbeads are designed for the positive selection or negative selection of human cytotoxic CD8+ T cells from fresh or frozen human peripheral blood mononuclear cells (PBMCs). The CD8 antigen forms a complex together with the T cell receptor and acts as an accessory molecule in the recognition of MHC class I/peptide complexes by the TCR heterodimer on CD8+ cytotoxic T cells. It is predominantly expressed on the surface of cytotoxic T cells. The magnetic nBeads are conjugated with monoclonal antibodies targeting human CD8 protein, enabling CD8+ cells to be labeled with the specific antibodies and magnetic particles, and separated using the separation columns and magnets.

  • Storage

    For long term storage, the product should be stored in liquid state at -20°C or below. Stability upon receipt: Stable for 24 months at -20 °C or below; Stable for 9 months at 2-8 °C under sterile conditions.

    Please protect from light and avoid repeated freeze-thaw cycles.

  • Sterility

    Negative

  • Endotoxin

    Less than 2 EU per mL by the LAL method / rFC method.

  • Mycoplasma

    Negative

  • Important Note

    This product is for research use only and not intended for therapeutic or in vivo diagnostic use.

  • Formulation

    Supplied in PBS buffer containing EDTA, rHSA and Poloxamer 188.

  • ACRO Quality Management System

    1. QMS(ISO, GMP)
    2. Quality Advantages
    3. Quality Control Process

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Data Display

  • Application Data

     CD8 APPLICATION DATA

    Superior Cell Separation Performance
    Separation performance was evaluated using samples containing 1×10⁷ human PBMCs, processed with CD8 microbeads from Acro, Company M, or Company T at recommended dosages. Positive and negative fractions were collected, and 1×10⁶ cells from each fraction were immunostained with PE-conjugated anti-human CD8 antibody and 7-AAD, followed by flow cytometric analysis. Data indicated that Acro microbeads achieved a final purity of 98% (baseline: 27.15%), with a target cell residue of only 1.69% in the negative fraction. These findings validate outstanding separation performance, confirming an optimal balance of purity and recovery relative to competitor benchmarks.

  •  CD8 APPLICATION DATA

    Comparison of Cell Separation Performances
    Isolation efficacy was validated using samples containing 1×10⁷ human PBMCs processed with the recommended dosage of Cellectra™ Human CD8 NanoSort Microbeads, in parallel with product from Company M and Company T. Comparative analysis demonstrated that Acro NanoSort Microbeads achieved higher cell recovery rates than Company M/T, while purity and cell viability were comparable to Company M and superior to Company T.

  •  CD8 APPLICATION DATA

    Cell Separation Performances of Different Donors
    The separation performances of human PBMCs exhibited minor inter-donor variability, yet consistently maintained high purity and cell recovery across all donors (Routinely tested).

  •  CD8 APPLICATION DATA

    Cell Separation Performances after Freeze-Thawing and Accelerated Aging at 37℃
    Freeze-thaw stability was verified by subjecting the microbeads to 2–3 cycles prior to separation testing. Comparative analysis against the standard batch confirmed that purity and cell recovery were maintained at baseline specifications, demonstrating robust stability. To ensure prolonged shelf life, storage at -20°C or below is recommended upon receipt (however, repeated freeze-thaw cycles are not advised for routine operational use).
    Accelerated aging studies were conducted at 37°C to evaluate long-term stability profiles. Following 7 and 14-day incubation periods, the microbeads sustained high purity and cell recovery performance during PBMC separation. These data substantiate product stability and validate the established shelf-life specifications.

  •  CD8 APPLICATION DATA

    Batch-to-Batch Consistency
    Manufacturing reproducibility was verified by conjugating three batches of CD8 NanoSort Microbeads with three corresponding batches of synthesized magnetic beads. Performance testing for human PBMC separation was conducted without dose adjustment; final dosage optimization will be completed during the pre-launch phase. Data indicates that all batches achieved consistent high purity and recovery, establishing reliable batch-to-batch consistency.

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Publish Comment

Frontier Progress

 
Drug Development Progress
  • English Name:

    Cluster of differentiation 8

  • Category:

  • Listed Drugs Count:

    0 Details

  • Clinical Drugs Count:

    18 Details

  • Highest R&D Stage:

    Phase 3 Clinical

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