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Cat. No. ARG35639

ABCB10 Knockout 143B Polyclonal Cells

  • Product Type:

    Polyclonal Cell Population

  • Species:

    Homo sapiens (Human)

  • Tissue Source:

    Bone

  • Disease:

    Osteosarcoma

The ABCB10 Knockout 143B Polyclonal Cells provide a CRISPR/Cas9-edited polyclonal population in human osteosarcoma cells, disrupting the mitochondrial transporter ABCB10. This gene is essential for heme biosynthesis and oxidative stress defense, regulated by GATA1, GATA2, and NRF2, and functionally linked to SLC25A37 and FECH. The knockout model enables investigation of erythropoiesis, mitochondrial iron transport, and redox signaling in a p53-mutant cancer context. Suitable for techniques such as heme quantification, ROS assays, flow cytometry, and Seahorse analysis, this product supports drug discovery for porphyria, anemia, and mitochondrial dysfunction.

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Shipping Info:

Cryopreserved in vials and shipped on dry ice


Disclaimer:

For Research Use Only

  • Characteristics

    Host Cell

    143B

    Age

    13 years

    Gene Name

    ABCB10

    Gene Identifier

    NCBI Gene ID 23456

    Morphology

    Epithelial-like

    Growth Mode

    Adherent

    Storage

    Liquid nitrogen (LN2)

  • Culture Conditions

    Growth medium

    DMEM/F12

    Supplement(s)

    10% Fetal Bovine Serum, 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

ABCB10 Knockout 143B Polyclonal Cells are a CRISPR/Cas9-edited polyclonal knockout cell population targeting the ABCB10 gene in the human 143B osteosarcoma cell line. The polyclonal format provides a heterogeneous loss-of-function model without single-cell cloning, ideal for functional genomics and drug discovery studies that benefit from population-level analysis.

The host 143B cell line is a widely used human osteosarcoma model with epithelial morphology and mutant p53. Derived from a primary bone tumor, these cells are central to bone cancer research, including investigations of metastasis, therapeutic resistance, and metabolic reprogramming, making them a relevant background for mitochondrial gene knockout studies.

ABCB10 encodes a mitochondrial inner membrane transporter essential for heme biosynthesis. It stabilizes mitoferrin-1 (SLC25A37), facilitating mitochondrial iron import, and is transcriptionally controlled by GATA1, GATA2, and NFE2L2 (NRF2). ABCB10 interacts with ferrochelatase (FECH) and SUCLG1, and its downstream targets include ALAS2 and HMOX1. Loss of ABCB10 disrupts heme production and exacerbates oxidative stress, linking its function to disorders such as erythropoietic protoporphyria and microcytic anemia.

In 143B cells, ABCB10 knockout enables dissection of mitochondrial iron transport in osteosarcoma metabolism. The p53-mutant background, coupled with disrupted heme synthesis, may unmask vulnerabilities to oxidative damage and ferroptosis. This model supports analysis of how mitochondrial transporter defects influence cell proliferation, survival, and drug sensitivity in bone cancer, and can be used to explore redox signaling pathways intersecting with oncogenesis.

Recommended applications include erythropoiesis and heme metabolism assays, mitochondrial function studies, and oxidative stress profiling. Compatible techniques include western blotting, heme measurement, ROS detection, qPCR for erythroid markers, hemoglobin staining, flow cytometry, Seahorse analysis, and iron-55 uptake assays. The knockout population is also suitable for drug screening targeting porphyria or anemia. For further technical details or ordering information, please contact Ascent Research.

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