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Cat. No. ARG34556

HCK Knockout THP-1 Polyclonal Cells

  • Product Type:

    Polyclonal Cell Population

  • Species:

    Homo sapiens (Human)

  • Tissue Source:

    Blood (peripheral blood)

  • Disease:

    Acute monoblastic leukemia

HCK Knockout THP-1 Polyclonal Cells provide a CRISPR/Cas9-edited population model for studying HCK function in myeloid biology. Derived from the THP-1 acute monocytic leukemia cell line, these polyclonal knockout cells enable investigation of HCK-dependent signaling through integrin and immune receptors, with key effectors including Syk, PI3K, and NF-??B. Applications include analysis of phagocytosis, adhesion, cytokine secretion, and drug screening for Src kinase inhibitors. This model supports immunology, inflammation, and leukemia research, offering a versatile tool for Western blotting, phagocytosis assays, ELISA, and phospho-kinase profiling.

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Shipping Info:

Cryopreserved in vials and shipped on dry ice


Disclaimer:

For Research Use Only

  • Characteristics

    Host Cell

    THP-1

    Cell Type

    Monocyte cell line

    Sex of Donor

    Male

    Age

    1 year

    Derived From Site

    In situ; Peripheral blood

    Gene Name

    HCK

    Gene Identifier

    NCBI Gene ID 3055

    Growth Mode

    Suspension

    Storage

    Liquid nitrogen (LN2)

  • Culture Conditions

    Growth medium

    RPMI 1640

    Supplement(s)

    10% Fetal Bovine Serum, 50uM β-mercaptoethanol, 1% Penicillin-Streptomycin Solution

    Temperature

    37°C

    Atmosphere

    5% CO₂

  • Quality Control

    Sterility testing

    The bacterial, yeast, and fungi are not detected in these cells by daily monitor.

    Mycoplasma testing

    Negative for mycoplasma through PCR analysis

  • Disclaimer

    Intended Use

    This product is intended for laboratory in vitro use only. lt is not intended for diagnostic, therapeutic, or clinical applications.

    Disclaimer

    Ascent Research endeavors to provide accurate and up-to-date product information. However, no warranties or representations are made regarding its completeness or reliability. References to scientific literature and patents are for informational purposes only, and the customer assumes sole responsibility for verifying their accuracy.

    By accepting this product, the customer acknowledges and agrees to assume all risks associated with its receipt, handling, storage, disposal, and use, including compliance with all applicable safety and environmental regulations and precautions. Relevant laws, regulations, and ethical guidelines must be followed in conducting any research, modifications, or derivatives derived from this product.

    This product is provided "AS IS", and except as expressly stated herein, Ascent Research disclaims all other warranties, express or implied. Under no circumstances shall Ascent Research, its affiliates, or representatives be liable for indirect, incidental, consequential, or punitive damages arising from the use of this material. While Ascent Research employs rigorous quality control measures, we shall not be held responsible for damages resulting from misidentification or misinterpretation of the provided materials.

Description

HCK Knockout THP-1 Polyclonal Cells are a CRISPR/Cas9-edited polyclonal population of THP-1 cells harboring targeted disruption of the HCK gene. This heterogeneous knockout pool facilitates loss-of-function studies while avoiding clonal selection biases, making it suitable for population-level assays that require biological variability.

The THP-1 cell line, derived from the peripheral blood of a 1-year-old male with acute monocytic leukemia, is a classical model for monocyte/macrophage differentiation. Upon phorbol ester or cytokine stimulation, THP-1 cells differentiate into macrophage-like cells, exhibiting adhesion, phagocytosis, and secretion of inflammatory mediators. This background is ideal for dissecting myeloid signaling and innate immunity.

HCK is a myeloid-dominant Src family tyrosine kinase that transduces signals from integrin receptors, Fc?? receptors, TLRs, and cytokine receptors (G-CSF, GM-CSF). Once activated, HCK phosphorylates downstream targets such as Syk, PI3K, Vav, and paxillin, triggering MAPK cascades, NF-??B, and STAT3. These pathways collectively regulate phagocytosis, adhesion, and pro-inflammatory cytokine production, including TNF-?? and IL-6.

Disruption of HCK in THP-1 cells attenuates integrin-mediated adhesion, Fc receptor-dependent phagocytosis, and TLR-induced NF-??B signaling, leading to reduced cytokine secretion. This knockout model thus enables precise interrogation of HCK??s contributions to myeloid leukemia signaling, inflammatory disease mechanisms, and Src kinase pathway function. It also serves as a valuable system for screening Src kinase inhibitors and evaluating their effects on innate immune responses.

Researchers can employ this polyclonal product in a variety of assays: Western blotting and RT-qPCR for knockout verification, phagocytosis assays with fluorescent particles, cytokine ELISA (e.g., TNF-??, IL-6), transwell migration, phospho-kinase arrays, and co-immunoprecipitation of ITAM-containing receptor complexes. Flow cytometry can assess activation markers and differentiation status. Applications range from basic inflammation research to drug discovery for myeloid malignancies. For technical inquiries or custom orders, contact Ascent Research.

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