Gene: SMARCD1
Official Full Name: SWI/SNF related BAF chromatin remodeling complex subunit D1provided by HGNC
Gene Summary: The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI and has sequence similarity to the yeast Swp73 protein. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO05949 | SMARCD1 Knockout cell line (HeLa) | Human | SMARCD1 | 1:3~1:6 | Negative | Online Inquiry |
KO05950 | SMARCD1 Knockout cell line (HCT 116) | Human | SMARCD1 | 1:2~1:4 | Negative | Online Inquiry |
KO05951 | SMARCD1 Knockout cell line (HEK293) | Human | SMARCD1 | 1:3~1:6 | Negative | Online Inquiry |
KO05952 | SMARCD1 Knockout cell line (A549) | Human | SMARCD1 | 1:3~1:4 | Negative | Online Inquiry |
SMARCD1 Gene Knockout Cell Lines are genetically engineered human cell lines designed to specifically eliminate the expression of the SMARCD1 gene, which plays a crucial role in chromatin remodeling and gene expression regulation. These knockout cell lines utilize CRISPR/Cas9 technology to achieve precise disruption of the SMARCD1 gene, providing a robust tool for researchers investigating the molecular mechanisms of gene regulation, cellular differentiation, signal transduction, and other essential biological processes.
The key function of SMARCD1 is its involvement in the assembly of the SWI/SNF chromatin remodeling complex, which modulates the accessibility of chromatin to transcription factors, thereby influencing gene expression patterns. By utilizing these knockout cell lines, researchers can explore the resultant phenotypic changes attributable to the absence of SMARCD1. This includes studies on cellular proliferation, apoptosis, and differentiation pathways that may be altered due to modifications in chromatin structure.
The scientific importance of SMARCD1 Gene Knockout Cell Lines extends across various research domains, including cancer biology, developmental biology, and epigenetics. In clinical settings, understanding the role of SMARCD1 can aid in deciphering its implications in tumorigenesis and potential therapeutic targets, making these cell lines a vital resource for both basic and applied research.
Compared to traditional methods of gene silencing, such as RNA interference or chemical inhibitors, our SMARCD1 Gene Knockout Cell Lines provide a permanent and precise genetic alteration, ensuring more reproducible results and enabling long-term studies on stable cell populations. This specificity allows for a better understanding of the functional consequences of the gene's loss, minimizing off-target effects that can confound experimental outcomes.
Researchers and clinicians alike will find value in eliminating guesswork regarding gene function through these knockout lines, facilitating clear hypothesis testing in cellular and molecular biology. Ultimately, our company is committed to advancing research in genetics and cell biology, backed by expert knowledge and a broad portfolio of related genetic tools, ensuring customers have access to high-quality products that meet the demands of cutting-edge scientific inquiry.
Please note that all services are for research use only. Not intended for any clinical use.
If your question is not addressed through these resources, you can fill out the online form below and we will answer your question as soon as possible.
There is no product in your cart. |
CD Biosynsis is a leading customer-focused biotechnology company dedicated to providing high-quality products, comprehensive service packages, and tailored solutions to support and facilitate the applications of synthetic biology in a wide range of areas.