Gene: STX10
Official Full Name: syntaxin 10provided by HGNC
Gene Summary: This gene belongs to the syntaxin family and encodes a soluble N-ethylmaleimide sensitive factor attachment protein receptor (SNARE). The encoded protein is involved in docking and fusion events at the Golgi apparatus. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2012]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO05497 | STX10 Knockout cell line (HeLa) | Human | STX10 | 1:3~1:6 | Negative | Online Inquiry |
KO05498 | STX10 Knockout cell line (HCT 116) | Human | STX10 | 1:2~1:4 | Negative | Online Inquiry |
KO05499 | STX10 Knockout cell line (HEK293) | Human | STX10 | 1:3~1:6 | Negative | Online Inquiry |
KO05500 | STX10 Knockout cell line (A549) | Human | STX10 | 1:3~1:4 | Negative | Online Inquiry |
STX10 Gene Knockout Cell Lines are specifically engineered cellular models designed to investigate the role of the syntaxin 10 (STX10) gene in various biological processes. These cell lines are developed through the CRISPR/Cas9 genome editing technology, which allows for precise gene disruption, enabling researchers to study the functional consequences of the loss of STX10 expression. By providing a controlled system for gene knockout, these cell lines facilitate the elucidation of STX10’s contributions to cellular mechanisms, such as exocytosis and vesicular transport, which are critical in both normal physiology and disease states.
The primary mechanism underlying the functionality of STX10 Gene Knockout Cell Lines involves the targeted alteration of the STX10 gene, resulting in complete absence of the protein it encodes. This knockout enables researchers to assess changes in cellular behavior, biochemical pathways, and interactions with other proteins, thus painting a clearer picture of STX10’s role in health and disease. Such insights are particularly pertinent in the fields of neurobiology, cancer research, and immunology, where the dysregulation of vesicle transport can have profound effects.
Scientifically, these cell lines hold significant value in research and clinical settings. They may be employed to explore drug responses, identify novel therapeutic targets, or even develop gene therapy strategies by providing insight into how STX10 knockout influences disease phenotypes. Compared to other available models, STX10 Gene Knockout Cell Lines offer unparalleled specificity, reproducibility, and the potential for high-throughput applications, making them a more efficient tool for gene functional studies.
The advantages of using STX10 Gene Knockout Cell Lines are further exemplified by their ease of use, as they can be cultured under standard conditions and are compatible with most assays, including high-content screening. Their availability allows researchers to bypass the time-consuming and costly processes associated with creating custom genetic models. For researchers and clinicians alike, the ability to precisely study the implications of STX10 deletion positions these cell lines as an essential asset in molecular biology investigations.
Our company specializes in the development of innovative biological products, underscored by a commitment to quality and scientific rigor. Our expertise in gene editing technologies ensures that products like the STX10 Gene Knockout Cell Lines adhere to stringent standards, providing researchers with reliable tools that accelerate discovery and contribute to advancing biological science.
Please note that all services are for research use only. Not intended for any clinical use.
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