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CC2D1B Knockout Cell Lines

Gene: CC2D1B

Official Full Name: coiled-coil and C2 domain containing 1Bprovided by HGNC

Gene Summary: Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to act upstream of or within negative regulation of transcription by RNA polymerase II. Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2025]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO38439 CC2D1B Knockout cell line (HeLa) Human CC2D1B 1:3~1:6 Negative Online Inquiry
KO38440 CC2D1B Knockout cell line (HCT 116) Human CC2D1B 1:2~1:4 Negative Online Inquiry
KO38441 CC2D1B Knockout cell line (HEK293) Human CC2D1B 1:3~1:6 Negative Online Inquiry
KO38442 CC2D1B Knockout cell line (A549) Human CC2D1B 1:3~1:4 Negative Online Inquiry

Background

CC2D1B Gene Knockout Cell Lines are genetically engineered cell lines specifically designed to lack the CC2D1B gene, a protein-coding gene implicated in various cellular processes, including neuronal development and synaptic signaling. These knockout models serve as invaluable tools for elucidating the biological roles of CC2D1B, as well as its involvement in pathologies, such as neurodevelopmental disorders and certain cancers.

The primary function of CC2D1B Gene Knockout Cell Lines is to allow researchers to study the gene's role by examining phenotypic changes when the gene is absent. Through techniques such as CRISPR/Cas9 gene editing, CC2D1B can be precisely disrupted, thus enabling comprehensive studies on gene function, signaling pathways, and cellular mechanisms. Researchers can assess alterations in cell proliferation, differentiation, and apoptosis that stem from the loss of CC2D1B, offering insights into its physiological and pathological relevance.

From a scientific viewpoint, these knockout cell lines hold significant value in both basic and applied research settings. Their applications include drug discovery, disease modeling, and the identification of potential therapeutic targets, particularly in studies aimed at understanding neurodevelopmental conditions or malignancies associated with CC2D1B dysregulation. Utilizing these cell lines can accelerate discoveries in pharmacogenomics and personalized medicine, potentially leading to improved treatment strategies.

Compared to conventional wild-type cell lines, the CC2D1B knockout variants provide a more refined approach to studying gene function, enabling researchers to engage in comparative analyses that can reveal critical insights into gene interactions and cellular responses. This specificity can enhance the reliability of research outcomes and reduce the time required for validation.

For researchers and clinicians focusing on genetic and molecular biology, adopting CC2D1B Gene Knockout Cell Lines into their studies offers a robust opportunity to advance understanding and innovations in genetic research. Our company, with extensive expertise in genetic engineering and cell line development, is committed to providing high-quality biological products that empower researchers to explore crucial scientific inquiries and drive breakthroughs in health and disease.

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

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