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ARHGAP35 Knockout Cell Lines

Gene: ARHGAP35

Official Full Name: Rho GTPase activating protein 35provided by HGNC

Gene Summary: The human glucocorticoid receptor DNA binding factor, which associates with the promoter region of the glucocorticoid receptor gene (hGR gene), is a repressor of glucocorticoid receptor transcription. The amino acid sequence deduced from the cDNA sequences show the presence of three sequence motifs characteristic of a zinc finger and one motif suggestive of a leucine zipper in which 1 cysteine is found instead of all leucines. The GRLF1 enhances the homologous down-regulation of wild-type hGR gene expression. Biochemical analysis suggests that GRLF1 interaction is sequence specific and that transcriptional efficacy of GRLF1 is regulated through its interaction with specific sequence motif. The level of expression is regulated by glucocorticoids. [provided by RefSeq, Jul 2008]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO37501 ARHGAP35 Knockout cell line (HeLa) Human ARHGAP35 1:3~1:6 Negative Online Inquiry
KO37502 ARHGAP35 Knockout cell line (HCT 116) Human ARHGAP35 1:2~1:4 Negative Online Inquiry
KO37503 ARHGAP35 Knockout cell line (HEK293) Human ARHGAP35 1:3~1:6 Negative Online Inquiry
KO37504 ARHGAP35 Knockout cell line (A549) Human ARHGAP35 1:3~1:4 Negative Online Inquiry

Background

ARHGAP35 Gene Knockout Cell Lines are genetically engineered cellular models that lack the expression of the ARHGAP35 gene, which encodes a Rho GTPase-activating protein. By creating a knockout of this gene, researchers can investigate the protein's role in cellular processes such as cytoskeletal dynamics, migration, apoptosis, and signal transduction pathways. The absence of ARHGAP35 in these cell lines allows for the detailed study of its functional contributions in normal physiological processes and in various disease states, particularly cancer, where changes in Rho GTPase activity can significantly influence tumor progression.

The mechanism of these knockout cell lines involves the targeted disruption of the ARHGAP35 gene through advanced techniques such as CRISPR/Cas9 technology. This precise gene-editing approach ensures that the resultant cell lines are devoid of ARHGAP35 expression, providing a robust platform for elucidating its pathway interactions and regulatory mechanisms. Such insights are invaluable for identifying potential therapeutic targets and strategies in the context of diseases associated with aberrant Rho GTPase signaling.

The scientific importance of ARHGAP35 Gene Knockout Cell Lines extends into various research domains, including cancer biology, immunology, and developmental biology. These models facilitate the exploration of fundamental cellular processes and enable researchers to assess how alterations in ARHGAP35 influence cellular behavior in vitro. Their application in drug screening and the development of targeted therapies further underscore their relevance in clinical research.

Compared to traditional cell lines or non-specific gene knockouts, the ARHGAP35 knockout models provide a significant advantage by offering specific insights into the role of ARHGAP35 without the confounding effects of other genetic elements. This specificity enhances the reliability of experimental outcomes and promotes a deeper understanding of cell signaling pathways.

For researchers and clinicians focused on unraveling the complexities of disease mechanisms or developing novel therapeutic strategies, the ARHGAP35 Gene Knockout Cell Lines represent a valuable resource. They support innovative research approaches and contribute to the advancement of targeted treatments.

With years of experience and a commitment to excellence, our company specializes in providing high-quality biologically-relevant products that empower scientific discovery. We pride ourselves on delivering precise solutions that meet the evolving needs of researchers and clinicians alike.

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

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