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Cat. No. ARG0275

KLF7 Knockout HCT 116 Cell Line

  • Product Type:

    Genome-edited Cells

  • Tissue Source:

    Large intestine (colon)

  • Disease:

    Carcinoma

  • Gene Species:

    Homo sapiens (Human)

The KLF7 Knockout HCT 116 Cell Line is a CRISPR/Cas9-edited knockout cell line in the HCT 116 colorectal carcinoma background. KLF7 is a Kr??ppel-like factor transcription factor regulated by ??-catenin/TCF and TGF-?? signaling; it controls targets such as CDKN1A (p21) and CDH1 (E-cadherin) to modulate cell proliferation and adhesion. The host HCT 116 cells harbor KRAS G13D and mismatch repair mutations, providing a relevant model for colorectal cancer studies. This knockout line is designed for investigating KLF7 function in cell cycle regulation, apoptosis, migration, and drug response. Representative applications include RNA-seq, RT-qPCR, Western blotting, flow cytometry, and transwell assays. It is an essential tool for research on Wnt/??-catenin, MAPK/ERK, and PI3K/AKT pathway interactions in colorectal carcinoma.

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Shipping Info:

Cryopreserved in vials and shipped on dry ice


Disclaimer:

For Research Use Only

  • Characteristics

    Host Cell

    HCT 116

    Morphology

    Epithelial-like

    Age

    Adult

    Sex of Donor

    Male

    Gene Name

    KLF7

    Gene Species

    Homo sapiens (Human)

    Gene Identifier

    NCBI Gene ID 8609

  • Culture Conditions

    Temperature

    37°C

    Atmosphere

    5% CO₂

  • Quality Control

    Sterility testing

    Daily monitoring confirms that the cells are free from bacterial, yeast, and fungal contamination.

    Mycoplasma testing

    Negative for mycoplasma through PCR analysis

    Pathogens

    Cells tested negative for HIV-1, HBV, and HCV.

  • 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

The KLF7 Knockout HCT 116 Cell Line is a CRISPR/Cas9-edited knockout cell line generated from the HCT 116 human colorectal carcinoma cell line. This loss-of-function model enables the study of KLF7, a Kr??ppel-like factor transcription factor, in a colorectal cancer context. The cell line is produced by CRISPR/Cas9-mediated disruption of the KLF7 gene, providing a stable, homogenous population suitable for reproducible functional assays.

HCT 116 is a well-characterized colorectal carcinoma cell line with mutations in MLH1 and MSH3 mismatch repair genes and a KRAS G13D oncogenic mutation, leading to microsatellite instability. Its epithelial morphology and robust growth support diverse in vitro applications, including proliferation, migration, and drug sensitivity assays. The KLF7 knockout derivative maintains the parental genetic background, allowing direct comparison with wild-type HCT 116 cells.

KLF7 functions as a context-dependent transcriptional activator or repressor that binds GC-rich promoter elements. It is regulated by upstream signals: the ??-catenin/TCF complex activates KLF7 expression downstream of Wnt, while TGF-??1 also induces it, and miR-181a represses it. KLF7 directly regulates targets including CDKN1A (p21), CDH1 (E-cadherin), and CCND1 (cyclin D1), thereby controlling cell cycle and adhesion. It interacts with co-regulators such as p300/CBP, SIN3A, and HDAC complexes. Through these interactions, KLF7 integrates inputs from Wnt/??-catenin, TGF-??/SMAD, MAPK/ERK, and PI3K/AKT pathways.

In the HCT 116 background, KLF7 knockout likely alters p21 and E-cadherin expression, potentially enhancing proliferation and invasion. The KRAS G13D mutation and mismatch repair deficiency may synergize with KLF7 loss to drive tumorigenic phenotypes via MAPK/ERK signaling. This cell line thus allows dissection of KLF7’s role in cell cycle checkpoints, apoptosis, and epithelial-mesenchymal transition, and its interplay with ??-catenin/TCF4 effectors. It also enables exploration of metabolic dysregulation links via ADIPOQ.

The KLF7 Knockout HCT 116 Cell Line is suited for cell proliferation (MTT), cell cycle (flow cytometry), apoptosis (Annexin V), and migration (transwell) assays. It can be used in RNA-seq, RT-qPCR, Western blotting, and immunofluorescence for gene and protein expression profiling. Luciferase reporter assays validate KLF7 transcriptional activity, while co-immunoprecipitation examines interactions with SMAD proteins or p300/CBP. This model is valuable for drug screens targeting MAPK, PI3K/AKT, or ??-catenin pathways, and for synthetic lethality studies in mismatch repair-deficient cancers. For further information, please contact Ascent Research.

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