Gene: SFMBT1
Official Full Name: Scm like with four mbt domains 1provided by HGNC
Gene Summary: This gene shares high similarity with the Drosophila Scm (sex comb on midleg) gene. It encodes a protein which contains four malignant brain tumor repeat (mbt) domains and may be involved in antigen recognition. [provided by RefSeq, Jun 2012]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO22517 | SFMBT1 Knockout cell line (HeLa) | Human | SFMBT1 | 1:3~1:6 | Negative | Online Inquiry |
KO22518 | SFMBT1 Knockout cell line (HCT 116) | Human | SFMBT1 | 1:2~1:4 | Negative | Online Inquiry |
KO22519 | SFMBT1 Knockout cell line (HEK293) | Human | SFMBT1 | 1:3~1:6 | Negative | Online Inquiry |
KO22520 | SFMBT1 Knockout cell line (A549) | Human | SFMBT1 | 1:3~1:4 | Negative | Online Inquiry |
SFMBT1 Gene Knockout Cell Lines are genetically engineered cell lines characterized by the targeted deletion of the SFMBT1 gene, a critical player in cellular processes including cell differentiation, proliferation, and developmental regulation. By selectively disrupting the SFMBT1 gene, these knockout models serve as powerful tools for elucidating the gene's functional role within various biological contexts, particularly in studying its implications in cancer biology and developmental disorders.
The key functions of the SFMBT1 Gene Knockout Cell Lines lie in their ability to mimic the in vivo loss-of-function scenarios that allow researchers to dissect the molecular pathways mediated by SFMBT1. The mechanisms by which these knockout cell lines operate involve the elimination of gene expression through CRISPR/Cas9 or other gene-editing technologies, leading to observable phenotypic changes that can be analyzed for modifications in growth patterns, signaling pathways, and gene regulation.
From a scientific viewpoint, these cell lines hold significant importance in both basic and applied research. They provide essential insights into the roles of SFMBT1 in various cellular mechanisms, making them valuable for drug discovery, functional genomics studies, and the investigation of gene-environment interactions. In clinical settings, understanding the SFMBT1 regulatory network can inform therapeutic strategies for diseases where this gene is implicated.
Key advantages of our SFMBT1 Gene Knockout Cell Lines include their high specificity and reproducibility, which outperform conventional knockdown methods such as RNA interference that often result in incomplete knockouts and off-target effects. Furthermore, our product is validated through extensive characterization, ensuring reliability in experimental outcomes.
For researchers and clinicians aiming to deepen their understanding of gene function and its broader implications, the SFMBT1 Gene Knockout Cell Lines offer an unmatched resource that bridges experimental findings with potential clinical applications. With our commitment to advancing genetic research, we strive to provide high-quality, innovative biological products that empower the scientific community to make groundbreaking discoveries.
Please note that all services are for research use only. Not intended for any clinical use.
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