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TRIM7 Knockout Cell Lines

Gene: TRIM7

Official Full Name: tripartite motif containing 7provided by HGNC

Gene Summary: The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1, a B-box type 2, and a coiled-coil region. The protein localizes to both the nucleus and the cytoplasm, and may represent a participant in the initiation of glycogen synthesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2013]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO25660 TRIM7 Knockout cell line (HeLa) Human TRIM7 1:3~1:6 Negative Online Inquiry
KO25661 TRIM7 Knockout cell line (HCT 116) Human TRIM7 1:2~1:4 Negative Online Inquiry
KO25662 TRIM7 Knockout cell line (HEK293) Human TRIM7 1:3~1:6 Negative Online Inquiry
KO25663 TRIM7 Knockout cell line (A549) Human TRIM7 1:3~1:4 Negative Online Inquiry

Background

TRIM7 Gene Knockout Cell Lines are specialized experimental models designed to eliminate the expression of the TRIM7 gene, allowing researchers to study the gene's role in cellular processes and its relevance to various diseases. This product utilizes CRISPR-Cas9 technology to achieve targeted gene disruption, ensuring precise modifications to the genome without off-target effects. By knocking out TRIM7, scientists can observe phenotypic and molecular changes, thereby elucidating the gene's function in pathways such as immune response regulation and neurodegenerative diseases.

Key applications of TRIM7 Knockout Cell Lines span both fundamental research and potential therapeutic developments. In research settings, these cell lines provide valuable insight into the TRIM7-mediated mechanisms that contribute to cellular signaling and disease progression, aiding in the identification of novel drug targets. Clinically, understanding TRIM7 function can lead to advancements in treatment strategies for conditions like cancer and autoimmune disorders, where gene dysregulation plays a critical role.

The advantages of using TRIM7 Gene Knockout Cell Lines over traditional methods include their precision, reproducibility, and the ability to generate multiple knockout clones ensuring consistent experimental results. Unlike previous gene editing techniques, CRISPR-Cas9 allows for rapid generation of knockout models, facilitating accelerated research timelines.

Researchers and clinicians alike will find TRIM7 Gene Knockout Cell Lines invaluable tools for deciphering cellular mechanisms and driving innovative therapeutic discoveries. Our company prides itself on expertly producing high-quality biological products that meet the diverse needs of the research community. With a commitment to advancing scientific understanding, we empower researchers to unlock the mysteries of gene function and therapeutic potentials with precision.

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

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