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PBXIP1 Knockout Cell Lines

Gene: PBXIP1

Official Full Name: PBX homeobox interacting protein 1provided by HGNC

Gene Summary: The protein encoded by this gene interacts with the PBX1 homeodomain protein, inhibiting its transcriptional activation potential by preventing its binding to DNA. The encoded protein, which is primarily cytosolic but can shuttle to the nucleus, also can interact with estrogen receptors alpha and beta and promote the proliferation of breast cancer, brain tumors, and lung cancer. Several transcript variants encoding different isoforms have been found for this gene. More variants exist, but their full-length natures have yet to be determined. [provided by RefSeq, Dec 2015]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO15324 PBXIP1 Knockout cell line (HeLa) Human PBXIP1 1:3~1:6 Negative Online Inquiry
KO15325 PBXIP1 Knockout cell line (HCT 116) Human PBXIP1 1:2~1:4 Negative Online Inquiry
KO15326 PBXIP1 Knockout cell line (HEK293) Human PBXIP1 1:3~1:6 Negative Online Inquiry
KO15327 PBXIP1 Knockout cell line (A549) Human PBXIP1 1:3~1:4 Negative Online Inquiry

Background

PBXIP1 Gene Knockout Cell Lines are specialized cellular models engineered to lack the expression of the PBXIP1 gene, which encodes a protein involved in critical cellular processes including apoptosis, stem cell regulation, and oncogenesis. These knockout cell lines are created using advanced CRISPR/Cas9 technology, enabling precise genetic modifications that facilitate the exploration of PBXIP1’s role in various biological contexts.

The primary function of these cell lines is to provide a robust platform for researchers to investigate the effects of PBXIP1 deficiency on cellular behavior, signaling pathways, and gene expression networks. By utilizing these models, scientists can analyze the consequences of PBXIP1 loss in contexts such as cancer biology, metabolic diseases, and developmental processes, thus enhancing our understanding of its contributions to cell fate decisions.

The scientific importance of PBXIP1 Gene Knockout Cell Lines is underscored by their application in both research and clinical settings. In drug discovery, for instance, these models can be instrumental in assessing therapeutic targets and understanding mechanisms of drug resistance. Furthermore, they facilitate studies on tumorigenesis, offering insights that could lead to novel strategies for cancer treatment.

Compared to alternative methods such as siRNA or shRNA approaches, our PBXIP1 knockout cell lines provide a permanent and stable genetic edit, leading to more reliable and reproducible experimental outcomes. Additionally, the precision of the CRISPR/Cas9 system minimizes off-target effects, thereby ensuring that observed phenotypes are directly attributable to the PBXIP1 knockout.

Researchers and clinicians will find immense value in these cell lines, as they not only streamline experimental workflows but also enhance the quality of data obtained—ultimately driving forward knowledge in the field of molecular biology and therapeutic intervention. Our company brings a wealth of expertise in cellular engineering and genetic editing, ensuring that PBXIP1 Gene Knockout Cell Lines meet the highest standards of quality and reliability for advanced biological research.

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

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