Gene: RBM10
Official Full Name: RNA binding motif protein 10provided by HGNC
Gene Summary: This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO34277 | RBM10 Knockout cell line (HeLa) | Human | RBM10 | 1:3~1:6 | Negative | Online Inquiry |
KO34278 | RBM10 Knockout cell line (HCT 116) | Human | RBM10 | 1:2~1:4 | Negative | Online Inquiry |
KO34279 | RBM10 Knockout cell line (HEK293) | Human | RBM10 | 1:3~1:6 | Negative | Online Inquiry |
KO34280 | RBM10 Knockout cell line (A549) | Human | RBM10 | 1:3~1:4 | Negative | Online Inquiry |
RBM10 Gene Knockout Cell Lines are specialized cellular models designed to facilitate the study of the RBM10 gene's functional role in various biological processes. This innovative product involves the targeted gene editing of RBM10 using cutting-edge CRISPR/Cas9 technology, resulting in cell lines that exhibit loss of function of this gene. These knockout models are invaluable for researchers examining the gene's involvement in RNA processing, cellular stress responses, and its implications in diseases such as cancer.
The key mechanism behind these cell lines is the precise disruption of the RBM10 gene, leading to altered protein expression profiles and subsequent cellular pathways. By providing a clear framework for gene function and regulation, RBM10 knockout cell lines serve as powerful tools for elucidating the roles of RBM10 in cellular metabolism, proliferation, and differentiation. This genomic intervention allows researchers to explore downstream effects and contributions to pathological states without interference from the normal function of the gene.
The scientific importance of RBM10 Gene Knockout Cell Lines is underscored by their broad applications in both academic and clinical research. They enable the study of gene functionality, drug response, and the molecular underpinnings of diseases. Their use can lead to the identification of potential therapeutic targets, enhancing our understanding of health and disease states related to RBM10 malfunction.
What sets our RBM10 Gene Knockout Cell Lines apart from alternatives is the assurance of high efficiency and specificity in gene editing, which minimizes off-target effects—an essential aspect for producing reliable research data. Additionally, these cell lines come with comprehensive technical support, ensuring that researchers can maximize their experimental outcomes.
For researchers and clinicians seeking to dive deeper into the biological roles and clinical implications of the RBM10 gene, our products offer an essential gateway to new discoveries and innovations. With extensive experience in molecular biology product development, our company is dedicated to advancing research capabilities and enabling breakthroughs that can impact patient outcomes significantly.
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.