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ARSB Knockout Cell Lines

Gene: ARSB

Official Full Name: arylsulfatase Bprovided by HGNC

Gene Summary: Arylsulfatase B encoded by this gene belongs to the sulfatase family. The arylsulfatase B homodimer hydrolyzes sulfate groups of N-Acetyl-D-galactosamine, chondriotin sulfate, and dermatan sulfate. The protein is targeted to the lysozyme. Mucopolysaccharidosis type VI is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Dec 2016]

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Products Background

Products

Catalog Number Product Name Species Gene Passage ratio Mycoplasma testing Price
GP00591 ARSB gRNA1-gRNA2 KO plasmid ARSB $850
KO04296 ARSB Knockout cell line (HeLa) Human ARSB 1:3~1:6 Negative Online Inquiry
KO04297 ARSB Knockout cell line (HCT 116) Human ARSB 1:2~1:4 Negative Online Inquiry
KO04298 ARSB Knockout cell line (HEK293) Human ARSB 1:3~1:6 Negative Online Inquiry
KO04299 ARSB Knockout cell line (A549) Human ARSB 1:3~1:4 Negative Online Inquiry

Background

ARSB Gene Knockout Cell Lines are expertly engineered cell lines designed to provide researchers with the ability to study the biological functions and pathways associated with the arylsulfatase B (ARSB) gene. By using CRISPR/Cas9 gene-editing technology, these cell lines exhibit a complete knockout of the ARSB gene, enabling a thorough investigation into the physiological and pathological roles of ARSB in various cellular processes.

The primary function of ARSB involves the degradation of sulfated glycosaminoglycans, which are crucial for various cellular functions, including cell signaling and extracellular matrix maintenance. Understanding ARSB’s role within these pathways allows researchers to explore its implications in diseases such as mucopolysaccharidosis type VI (MPS VI), a lysosomal storage disorder linked to ARSB deficiency. These knockout cell lines therefore serve as powerful models for elucidating the molecular mechanisms underlying ARSB-related dysfunction and for screening therapeutic candidates aimed at correcting these deficiencies.

The scientific importance of ARSB Gene Knockout Cell Lines is underscored by their diverse applications in both basic research and clinical settings. Utilizing these cell lines can significantly enhance the understanding of ARSB's role in various disease mechanisms, leading to novel therapeutic strategies. Furthermore, these lines facilitate insights into the broader implications of sulfated glycosaminoglycans in physiological homeostasis, making them invaluable to researchers focused on cell biology, genetics, and therapeutic drug discovery.

Compared to traditional models, ARSB Gene Knockout Cell Lines offer precise and reliable gene-editing capabilities that allow for reproducibility and efficient studies of gene function without the confounding variables often present in wild-type cell lines. Additionally, they are readily available, enabling researchers to initiate their studies with minimal setup delays.

These cell lines stand out not only for their robust design but also for their adaptability across various experimental conditions, providing a vital resource for academics and clinicians alike. Researchers and healthcare professionals can gain a deeper understanding of ARSB-related pathologies, thereby improving patient outcomes through targeted therapies.

Our company brings extensive expertise in genetic engineering and cell line development, ensuring that all products, including the ARSB Gene Knockout Cell Lines, are of the highest quality and reliability. We are committed to supporting the scientific community's quest for knowledge with innovative and accessible biological products.

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

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