THP-1-cas9 Cell (Human Monocytic Leukemia)

THP-1-cas9 Cell (Human Monocytic Leukemia)

Catalog Number:
CT01567644ELE
Mfr. No.:
LM01300-Cas9
Price:
  • Size:
    Quantity:
    Add to Cart:
      • Overview
        • Species: human
          Cell Morphology: Suspension cells
          Complete Culture Medium Components: 1640 + 10% FBS + 0.05 mM2ME
          Mycoplasma testing: Negative
          Antibiotic Concentration: puromycin, 0.5ug/ml
          Cultivation Environment: 37°C, 5% CO₂
          Passage Ratio: 1/2 to 1/4 of the generations
          Frequency of Reproduction: 2-3 times/week
          Gene Expression: Cas9 protein, spCas9, CRISPR-Cas9 protein

          Product Advantages:
          • Efficiency and Convenience: A "ready-to-use" platform; simply import gRNA, operation is simple, editing efficiency is high, saving time and costs.
          • High-Throughput Screening: An ideal foundational platform for genome-wide CRISPR screening, used for systematic discovery of functional genes.
          • Consistency and Reproducibility: Consistent cell population genetic background, stable Cas9 expression, more reliable experimental results, and more rigorous control settings.
          • Functional Scalability: Cell lines expressing dCas9, high-fidelity Cas9, and other variants can be constructed to achieve multiple functions beyond gene knockout (regulation, imaging, etc.).

          Please contact us at for specific academic pricing.

          Background

          THP-1 cells phagocytose milk droplets and activated erythrocytes, but lack surface and cytoplasmic immunoglobulins. THP-1 cells can be induced to differentiate into monocytes using phorbol and TPA.

      • Properties
        • Categories
          Cas9 Stable Cell Lines

          * For Research Use Only.

      • Applications
        • Application Description
          The core advantage of the Cas9 cell line lies in its internalization of the core gene-editing tool, Cas9, into a stable component of the cell itself. This transforms complex gene-editing experiments into a more efficient, stable, and easily scalable standardized process, greatly advancing functional genomics research. It has wide applications in several cutting-edge biomedical fields, including gene knockout, CRISPR library screening, disease models, and drug development.