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SCNN1B Knockout Cell Lines

Gene: SCNN1B

Official Full Name: sodium channel epithelial 1 subunit betaprovided by HGNC

Gene Summary: Nonvoltage-gated, amiloride-sensitive, sodium channels control fluid and electrolyte transport across epithelia in many organs. These channels are heteromeric complexes consisting of 3 subunits: alpha, beta, and gamma. This gene encodes the beta subunit, and mutations in this gene have been associated with pseudohypoaldosteronism type 1 (PHA1), and Liddle syndrome. [provided by RefSeq, Apr 2009]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
KO35488 SCNN1B Knockout cell line (A549) Human SCNN1B 1:3~1:4 Negative Online Inquiry

Background

SCNN1B Gene Knockout Cell Lines represent a cutting-edge tool in molecular biology, designed to facilitate the study of the epithelial sodium channel (ENaC) family by providing researchers with genetically modified cell lines lacking the SCNN1B gene. ENaC plays a crucial role in ion transport and regulation of epithelial cell function, particularly in tissues such as the kidney and lung, where sodium balance is essential for physiological homeostasis. The knockout of the SCNN1B gene disrupts the normal function of ENaC, allowing for in-depth analysis of its role in various biological processes and disease states.

These cell lines operate through a precise CRISPR/Cas9 gene-editing approach, which ensures specific and reliable disruption of the SCNN1B gene. Researchers can observe changes in ion transport, cellular metabolism, and signaling pathways that are downstream of ENaC activity. This capability is particularly valuable in studies related to hypertension, cystic fibrosis, and pulmonary edema, where SCNN1B and ENaC function is implicated.

The scientific significance of SCNN1B Gene Knockout Cell Lines extends well into translational medicine, where understanding the pathology of diseases linked to ENaC dysfunction can aid the development of targeted therapies. Compared to traditional methodologies such as RNA interference or chemical inhibitors, utilizing knockout cell lines provides a more stable and reproducible model, ensuring that observed effects are directly attributed to the absence of the SCNN1B gene.

Advantages include high specificity, reduced off-target effects, and the ability to explore phenotype changes over time in a controlled environment. For researchers and clinicians focused on ion channel physiology and related pathologies, these knockout cell lines offer a unique and powerful resource that can expedite experimental timelines and enhance data quality.

Our company specializes in the development and provision of innovative biological tools for the scientific community. With extensive expertise in gene editing technologies and a commitment to advancing research, we are dedicated to supporting the advancement of knowledge in genetics and cell biology, ensuring our users stay at the forefront of scientific discovery.

Please note that all services are for research use only. Not intended for any clinical use.

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