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SMAD7 Knockout Cell Lines

Gene: SMAD7

Official Full Name: SMAD family member 7provided by HGNC

Gene Summary: The protein encoded by this gene is a nuclear protein that binds the E3 ubiquitin ligase SMURF2. Upon binding, this complex translocates to the cytoplasm, where it interacts with TGF-beta receptor type-1 (TGFBR1), leading to the degradation of both the encoded protein and TGFBR1. Expression of this gene is induced by TGFBR1. Variations in this gene are a cause of susceptibility to colorectal cancer type 3 (CRCS3). Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO11472 SMAD7 Knockout cell line (HeLa) Human SMAD7 1:3~1:6 Negative Online Inquiry
KO11473 SMAD7 Knockout cell line (HCT 116) Human SMAD7 1:2~1:4 Negative Online Inquiry
KO11474 SMAD7 Knockout cell line (HEK293) Human SMAD7 1:3~1:6 Negative Online Inquiry
KO11475 SMAD7 Knockout cell line (A549) Human SMAD7 1:3~1:4 Negative Online Inquiry

Background

SMAD7 Gene Knockout Cell Lines are advanced cellular models designed specifically to study the role of the SMAD7 gene in various biological processes, particularly in the context of TGF-β signaling pathways. The SMAD7 gene is a crucial inhibitor of TGF-β receptor signaling, and its knockout allows researchers to obtain insights into disease mechanisms, cellular differentiation, immune regulation, and cancer progression by revealing underlying molecular interactions that are compromised in various pathological states.

These cell lines function by employing CRISPR-Cas9 technology to precisely edit the SMAD7 gene, resulting in an effective knockout. This targeted approach ensures that the alterations are specific and reproducible, thereby providing a solid foundation for experimental consistency. The resulting cell lines exhibit altered responses to TGF-β, making them invaluable in elucidating the pathways propagated by this growth factor and its implication in fibrogenesis, inflammation, and tumorigenesis.

The scientific importance of SMAD7 Gene Knockout Cell Lines cannot be overstated; they serve as critical tools in preclinical research and drug development, aiding the identification of potential therapeutic targets and biomarkers for various diseases. Furthermore, these models offer a unique capability to screen compounds that may modulate TGF-β signaling, providing valuable data for clinicians and researchers working on fibrotic diseases or cancers that involve aberrant TGF-β signaling.

Compared to traditional cell lines that do not allow for direct manipulation of SMAD7, these knockout cell lines provide specific advantages by delivering clearer data regarding the functional consequences of SMAD7 loss. Additionally, they provide a more physiologically relevant environment, which can yield insights that are not observable in non-targeted models.

For researchers and clinicians focusing on TGF-β-related pathways, SMAD7 Gene Knockout Cell Lines present a compelling option, enhancing the quality of research efforts and potential clinical applications. Our company prides itself on its commitment to providing high-quality, cutting-edge biological tools and reagents, backed by extensive expertise in genetic engineering and cell line development, ensuring that our product offerings are of the highest standard in the market.

Please note that all services are for research use only. Not intended for any clinical use.

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