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CBL Knockout Cell Lines

Gene: CBL

Official Full Name: Cbl proto-oncogeneprovided by HGNC

Gene Summary: This gene is a proto-oncogene that encodes a RING finger E3 ubiquitin ligase. The encoded protein is one of the enzymes required for targeting substrates for degradation by the proteasome. This protein mediates the transfer of ubiquitin from ubiquitin conjugating enzymes (E2) to specific substrates. This protein also contains an N-terminal phosphotyrosine binding domain that allows it to interact with numerous tyrosine-phosphorylated substrates and target them for proteasome degradation. As such it functions as a negative regulator of many signal transduction pathways. This gene has been found to be mutated or translocated in many cancers including acute myeloid leukaemia, and expansion of CGG repeats in the 5' UTR has been associated with Jacobsen syndrome. Mutations in this gene are also the cause of Noonan syndrome-like disorder. [provided by RefSeq, Jul 2016]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO00990 CBL Knockout cell line (A549) Human CBL 1:3~1:4 Negative Online Inquiry
KO38678 CBL Knockout cell line (HeLa) Human CBL 1:3~1:6 Negative Online Inquiry
KO38679 CBL Knockout cell line (HCT 116) Human CBL 1:2~1:4 Negative Online Inquiry
KO38680 CBL Knockout cell line (HEK293) Human CBL 1:3~1:6 Negative Online Inquiry

Background

CBL Gene Knockout Cell Lines are engineered cellular models that have been specifically developed to abrogate the expression of the CBL gene, which is integral in various cellular signaling pathways. These cell lines are invaluable tools for researchers investigating the molecular mechanisms underlying signal transduction, cell proliferation, differentiation, and oncogenesis. By using CRISPR-Cas9 or other genetic modification techniques, these knockout cell lines allow for precise functional analysis of the CBL gene's role in cellular processes and disease states.

The primary function of CBL Gene Knockout Cell Lines is to facilitate in-depth studies of the CBL protein's contributions to pathophysiological conditions such as cancer and autoimmune diseases. Through gene knockout, researchers can observe the resultant phenotypic changes and signaling disruptions, providing critical insights into how disruptions in CBL function can lead to disease. This offers an essential framework for developing targeted therapies that address the dysregulation caused by aberrant CBL signaling.

Scientifically, the significance of these cell lines lies in their utility across diverse applications, from basic research to drug discovery. In clinical settings, understanding the implications of CBL gene dysfunction can pave the way for innovative therapeutic approaches. Researchers can employ these knockout models for high-throughput screening of drug candidates, assessing their efficacy in modulating CBL-related pathways.

When compared to alternatives like traditional siRNA knockdown, CBL Gene Knockout Cell Lines provide definitive changes at the genomic level, leading to more stable and reliable models for experimentation. This genomic editing leads to complete functional loss of the CBL protein, as opposed to temporary or partial silencing, allowing for clearer interpretation of results.

Given the ever-increasing demand for reliable cellular models in molecular biology, CBL Gene Knockout Cell Lines represent a critical asset for researchers aiming to elucidate the complexities of cellular signaling. They enable scientists to delve deeper into the functional consequences of gene loss, offering a gateway to potential breakthroughs in understanding and treating diseases.

Our company prides itself on delivering high-quality, innovative biological products. With a commitment to advancing research and clinical outcomes, we ensure that each CBL Gene Knockout Cell Line is meticulously validated and characterized, embodying our expertise in genetic engineering and cellular biology.

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

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