Gene: SCML1
Official Full Name: Scm polycomb group protein like 1provided by HGNC
Gene Summary: Predicted to enable chromatin binding activity and histone binding activity. Predicted to be involved in negative regulation of DNA-templated transcription. Predicted to be located in female germ cell nucleus and male germ cell nucleus. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO35504 | SCML1 Knockout cell line (HeLa) | Human | SCML1 | 1:3~1:6 | Negative | Online Inquiry |
KO35505 | SCML1 Knockout cell line (HCT 116) | Human | SCML1 | 1:2~1:4 | Negative | Online Inquiry |
KO35506 | SCML1 Knockout cell line (HEK293) | Human | SCML1 | 1:3~1:6 | Negative | Online Inquiry |
KO35507 | SCML1 Knockout cell line (A549) | Human | SCML1 | 1:3~1:4 | Negative | Online Inquiry |
SCML1 Gene Knockout Cell Lines are specialized laboratory models that have undergone precise genomic editing to eliminate the SCML1 gene, a key player in cellular processes such as proliferation, differentiation, and gene expression regulation. These knockout cell lines allow researchers to investigate the role of SCML1 in various biological contexts, providing insights into its function in cellular pathways and its implications in disease mechanisms.
The primary function of the SCML1 Gene Knockout Cell Lines lies in their ability to facilitate the study of cellular responses in the absence of SCML1. By removing this gene, researchers can examine alterations in gene expression patterns, cell cycle regulation, and differentiation processes. This knockout model serves as a powerful tool to elucidate the functional consequences of SCML1 deficiency and contributes to understanding its involvement in oncogenesis and other pathologies.
In research and clinical settings, SCML1 Gene Knockout Cell Lines provide valuable insights into tumor biology, development, and therapeutic responses. They enable scientists to explore drug efficacy, mechanisms of resistance, and potential therapeutic targets by mimicking clinical conditions devoid of the SCML1 gene. This knowledge is vital for advancing targeted therapies and improving patient outcomes in cancer treatment.
Compared to alternatives such as RNA interference or overexpression models, SCML1 Gene Knockout Cell Lines offer a more permanent and stable alteration of the gene, allowing for long-term study of cellular effects without the transient changes seen in other methods. Additionally, these knockout lines can be utilized across various platforms, including in vitro assays and in vivo studies, providing researchers with flexibility in experimental design.
The value of SCML1 Gene Knockout Cell Lines extends beyond basic research; they are instrumental for pharmaceutical companies, academic researchers, and clinical laboratories aiming to develop novel therapies. By enabling a deeper understanding of SCML1-related mechanisms, these cell lines can drive innovation in drug discovery, ultimately leading to more effective treatments for diseases where SCML1 plays a critical role.
Our company specializes in providing high-quality, fully characterized genetic tools, including SCML1 Gene Knockout Cell Lines, to support groundbreaking research and development in the life sciences. Our expertise in genetic engineering and commitment to quality ensures that our products meet the highest standards, empowering researchers to advance their work with confidence.
Please note that all services are for research use only. Not intended for any clinical use.
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