Gene: SLC26A11
Official Full Name: solute carrier family 26 member 11provided by HGNC
Gene Summary: This gene encodes a member of the solute linked carrier 26 family of anion exchangers. Members of this family of proteins are essential for numerous cellular functions including homeostasis and intracellular electrolyte balance. The encoded protein is a sodium independent sulfate transporter that is sensitive to the anion exchanger inhibitor 4,4'-diisothiocyanostilbene-2,2'-disulfonic acid. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Oct 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO14045 | SLC26A11 Knockout cell line (HeLa) | Human | SLC26A11 | 1:3~1:6 | Negative | Online Inquiry |
KO14046 | SLC26A11 Knockout cell line (HCT 116) | Human | SLC26A11 | 1:2~1:4 | Negative | Online Inquiry |
KO14047 | SLC26A11 Knockout cell line (HEK293) | Human | SLC26A11 | 1:3~1:6 | Negative | Online Inquiry |
KO14048 | SLC26A11 Knockout cell line (A549) | Human | SLC26A11 | 1:3~1:4 | Negative | Online Inquiry |
SLC26A11 Gene Knockout Cell Lines are specifically designed cellular models that have undergone targeted gene modification to inactivate the SLC26A11 gene. This gene encodes a member of the solute carrier family, known to play pivotal roles in anion transport, particularly in the exchange processes involving bicarbonate and chloride ions. By utilizing CRISPR-Cas9 technology for precise gene editing, these knockout cell lines serve as essential tools for elucidating the biological functions and pathways associated with SLC26A11.
The primary mechanisms governing the knockout functionality revolve around the complete absence of SLC26A11 protein, allowing researchers to investigate the subsequent physiological and biochemical alterations in cellular behavior. By examining changes in ion transport, cellular pH regulation, and subsequent metabolic effects, scientists can gain valuable insights into the gene's role in various physiological and pathological conditions, including its implications in metabolic disorders and diseases related to transport dysfunction.
The scientific importance of SLC26A11 Gene Knockout Cell Lines extends to fields such as pharmacology, genetics, and cell biology. These models are indispensable in research settings for studying the effectiveness of drug candidates targeting ion transport mechanisms and understanding disease pathways linked to SLC26A11 dysfunction. In clinical laboratories, these cell lines can facilitate the development and validation of novel therapeutics aimed at enhancing or correcting the ion transport processes essential for maintaining homeostasis.
What sets our SLC26A11 Gene Knockout Cell Lines apart from alternative offerings is their high specificity, reproducibility, and meticulous validation. Each cell line undergoes rigorous characterizations to confirm knockout efficiency and assess functional alterations, ensuring that researchers receive reliable models for their experiments. Moreover, our lines are compatible with various culture conditions, making them versatile tools for a wide range of biological investigations.
In a landscape where precise cellular models are critical for advancing scientific discovery, the SLC26A11 Gene Knockout Cell Lines provide unparalleled opportunities for researchers and clinicians alike. With our dedicated expertise in gene editing technologies and a commitment to delivering high-quality biological products, we empower scientists to uncover novel insights that can ultimately lead to innovative solutions in health and medicine.
Please note that all services are for research use only. Not intended for any clinical use.
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