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SCMH1 Knockout Cell Lines

Gene: SCMH1

Official Full Name: Scm polycomb group protein homolog 1provided by HGNC

Gene Summary: Predicted to enable chromatin binding activity and histone binding activity. Predicted to be involved in heterochromatin formation and negative regulation of DNA-templated transcription. Predicted to act upstream of or within anterior/posterior pattern specification; chromatin remodeling; and spermatogenesis. Predicted to be located in nucleoplasm. Predicted to be active in nucleus. [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
KO30089 SCMH1 Knockout cell line (HeLa) Human SCMH1 1:3~1:6 Negative Online Inquiry
KO30090 SCMH1 Knockout cell line (HCT 116) Human SCMH1 1:2~1:4 Negative Online Inquiry
KO30091 SCMH1 Knockout cell line (HEK293) Human SCMH1 1:3~1:6 Negative Online Inquiry
KO30092 SCMH1 Knockout cell line (A549) Human SCMH1 1:3~1:4 Negative Online Inquiry

Background

SCMH1 Gene Knockout Cell Lines represent a cutting-edge breakthrough in genetic research and therapeutic development. These engineered cellular models have been specifically designed to lack the SCMH1 gene, an essential regulator involved in chromatin remodeling and gene expression. By utilizing CRISPR-Cas9 technology, these cell lines provide a robust platform for investigating the functional implications of SCMH1 deficiency in various biological processes, including cellular differentiation, proliferation, and the onset of disease states.

The primary function of the SCMH1 Gene Knockout Cell Lines is to facilitate the precise dissection of the SCMH1 gene's role within cellular environments. By studying these models, researchers can elucidate the molecular mechanisms that underpin disorders associated with SCMH1 malfunctions, such as specific cancers and developmental defects. This gene knockout model enables scientists to identify downstream target genes and signaling pathways influenced by SCMH1, thus paving the way for potential therapeutic interventions.

The scientific importance of these cell lines cannot be overstated, as they offer invaluable insights into gene function and regulation. In clinical settings, the knowledge gained from such studies can translate into targeted treatments and personalized medicine approaches for patients with SCMH1-related pathologies. Compared to traditional cell lines, our SCMH1 Gene Knockout models provide an unparalleled specificity that allows for more accurate and reproducible experimental results.

Moreover, the unique capabilities of these knockout cell lines, including high adaptability for various experimental conditions and ease of use, stand out against other gene knockout models. Their ability to provide clear phenotypic changes in response to genetic manipulation makes them indispensable for both academic research and clinical applications.

Our commitment to genetic research excellence is reflected in our efficient design and production of these cell lines, ensuring that researchers and clinicians have access to the most reliable tools for their groundbreaking studies. With our state-of-the-art facilities and expert team, we stand ready to support the scientific community’s quest for discovery through innovative biological products.

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

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