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DYNC2I2 Knockout Cell Lines

Gene: DYNC2I2

Official Full Name: dynein 2 intermediate chain 2provided by HGNC

Gene Summary: This gene encodes a member of the WD repeat protein family. WD repeats are minimally conserved regions of approximately 40 amino acids typically bracketed by gly-his and trp-asp (GH-WD), which may facilitate formation of heterotrimeric or multiprotein complexes. Members of this family are involved in a variety of cellular processes, including cell cycle progression, signal transduction, apoptosis, and gene regulation. Defects in this gene are a cause of short-rib thoracic dysplasia 11 with or without polydactyly. [provided by RefSeq, Mar 2014]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO04480 DYNC2I2 Knockout cell line (HeLa) Human DYNC2I2 1:3~1:6 Negative Online Inquiry
KO04481 DYNC2I2 Knockout cell line (HCT 116) Human DYNC2I2 1:2~1:4 Negative Online Inquiry
KO04482 DYNC2I2 Knockout cell line (HEK293) Human DYNC2I2 1:3~1:6 Negative Online Inquiry
KO04483 DYNC2I2 Knockout cell line (A549) Human DYNC2I2 1:3~1:4 Negative Online Inquiry

Background

DYNC2I2 Gene Knockout Cell Lines are specialized genetically engineered cell lines designed to facilitate the functional study of the DYNC2I2 gene, which encodes the cytoplasmic dynein complex protein involved in intracellular transport and cellular localization processes. By creating a knockout model, researchers can effectively observe the consequences of DYNC2I2 gene inactivation, allowing for a clearer understanding of its role in cellular mechanisms and associated physiological processes.

The primary function of the DYNC2I2 Gene Knockout Cell Lines is to disrupt the normal expression of the DYNC2I2 gene, thereby enabling researchers to analyze alterations in cell behavior, including transport functions and organelle positioning. This is achieved through cutting-edge CRISPR/Cas9 gene-editing technology, which precisely targets and excises the gene of interest, resulting in a loss-of-function phenotype. Such cell lines provide a solid foundation for evaluating the effects of DYNC2I2 disruption on various biological pathways, cellular structures, and diseases.

The scientific importance of these cell lines extends to various areas including neurobiology, cancer research, and developmental biology. By utilizing DYNC2I2 knockout models, investigators can advance their understanding of the cellular pathologies associated with dynein dysfunction and its implications in disorders, such as neurodegenerative diseases and cancer metastasis. The insights gained from these studies may pave the way for novel therapeutic strategies or diagnostic tools.

Compared to alternative models, such as wild-type control cell lines or less specific gene silencing approaches, DYNC2I2 Gene Knockout Cell Lines offer targeted gene inactivation that is reproducible and provides a more definitive elucidation of gene function. Furthermore, they are validated for various assays, including proliferation, migration, and signaling pathway analyses, ensuring robust applicability across numerous experimental setups.

This product delivers substantial value to both academic and clinical researchers seeking accurate and reliable models for exploring gene function and associated conditions. Their ease of use, combined with the ability to generate meaningful data, fosters accelerated research and discovery.

Our company prides itself on extensive expertise in genetic engineering and cell line development, ensuring that our products meet the highest standards of quality and innovation, thus empowering researchers and clinicians to achieve their scientific objectives.

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

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