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PHF6 Knockout Cell Lines

Gene: PHF6

Official Full Name: PHD finger protein 6provided by HGNC

Gene Summary: This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by cognitive disability, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms. [provided by RefSeq, Jun 2010]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO05757 PHF6 Knockout cell line (HeLa) Human PHF6 1:3~1:6 Negative Online Inquiry
KO05758 PHF6 Knockout cell line (HCT 116) Human PHF6 1:2~1:4 Negative Online Inquiry
KO05759 PHF6 Knockout cell line (HEK293) Human PHF6 1:3~1:6 Negative Online Inquiry
KO05760 PHF6 Knockout cell line (A549) Human PHF6 1:3~1:4 Negative Online Inquiry

Background

PHF6 Gene Knockout Cell Lines are specially engineered cellular models that facilitate the study of the Polycomb Group Protein 6 (PHF6) by eliminating the expression of this gene. Implemented through precise gene editing techniques, such as CRISPR/Cas9, these cell lines allow researchers to dissect the functional role of PHF6 in various biological processes, including gene regulation, cell differentiation, and tumorigenesis. The knockout strategy ensures that researchers can observe phenotypic changes and molecular pathways influenced by the absence of PHF6, providing critical insights into its contributions to cancer biology and stem cell research.

The key mechanism behind the PHF6 Gene Knockout Cell Lines involves targeted disruption of the PHF6 gene, leading to an effective null phenotype. This is particularly valuable in understanding the pathophysiological implications of PHF6 mutations, which have been linked to various human cancers, including acute myeloid leukemia. Researchers utilizing these cell lines can perform comparative analyses with wild-type counterparts, adding granularity to their investigations into the gene's role in epigenetic regulation and cellular behavior.

The scientific importance of these knockout cell lines lies in their application within both basic and translational research. They serve as vital tools for elucidating the molecular mechanisms underpinning diseases associated with PHF6 dysfunction, making them indispensable in drug discovery efforts aimed at designing targeted therapies. Their usage can accelerate the transition from laboratory findings to clinical applications, providing a robust platform for testing therapeutic interventions that modulate PHF6 activity.

Compared to existing alternatives, PHF6 Gene Knockout Cell Lines offer unparalleled specificity and reliability due to their precise genetic modifications. This specificity ensures that researchers encounter fewer off-target effects, leading to more accurate experimental outcomes. Additionally, these cell lines are readily available and adaptable for high-throughput screening, fulfilling the growing demands of the research community for scalable solutions.

In summary, PHF6 Gene Knockout Cell Lines represent a significant advancement in the pursuit of understanding complex biological systems and disease pathways. Their targeted approach and effective gene disruption make them an invaluable resource for researchers and clinicians alike, providing the insights necessary to drive innovations in cancer treatment and genetic research. At [Your Company Name], we are committed to advancing scientific discovery through high-quality biological products, ensuring that researchers have the tools they need to succeed in their endeavors.

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

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