Gene: PAPSS1
Official Full Name: 3'-phosphoadenosine 5'-phosphosulfate synthase 1provided by HGNC
Gene Summary: Three-prime-phosphoadenosine 5-prime-phosphosulfate (PAPS) is the sulfate donor cosubstrate for all sulfotransferase (SULT) enzymes (Xu et al., 2000 [PubMed 10679223]). SULTs catalyze the sulfate conjugation of many endogenous and exogenous compounds, including drugs and other xenobiotics. In humans, PAPS is synthesized from adenosine 5-prime triphosphate (ATP) and inorganic sulfate by 2 isoforms, PAPSS1 and PAPSS2 (MIM 603005).[supplied by OMIM, Mar 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO33618 | PAPSS1 Knockout cell line (HeLa) | Human | PAPSS1 | 1:3~1:6 | Negative | Online Inquiry |
KO33619 | PAPSS1 Knockout cell line (HCT 116) | Human | PAPSS1 | 1:2~1:4 | Negative | Online Inquiry |
KO33620 | PAPSS1 Knockout cell line (HEK293) | Human | PAPSS1 | 1:3~1:6 | Negative | Online Inquiry |
KO33621 | PAPSS1 Knockout cell line (A549) | Human | PAPSS1 | 1:3~1:4 | Negative | Online Inquiry |
PAPSS1 Gene Knockout Cell Lines are specifically engineered cellular systems in which the PAPSS1 gene has been inactivated. This gene encodes for the enzyme 3'-phosphoadenosine-5'-phosphosulfate synthase 1, which plays a crucial role in the biosynthesis of sulfate-containing compounds necessary for various biological processes. By removing the functional PAPSS1 gene, these cell lines allow researchers to explore the downstream effects of sulfation deficiencies, providing insights into various metabolic pathways and cellular functions influenced by sulfation, including those involved in cell signaling, extracellular matrix formation, and hormonal regulation.
The primary mechanism by which these knockout cell lines operate is through the complete disruption of PAPSS1 enzymatic activity, resulting in altered cellular metabolism and impaired synthesis of sulfated molecules. This molecular alteration can be utilized by researchers to investigate the physiological consequences of sulfate deprivation, thus contributing to the understanding of diseases linked with sulfation dysregulation.
PAPSS1 Gene Knockout Cell Lines hold significant scientific importance in both basic and applied research, especially in the context of drug development, genetic disorders, and metabolic diseases. They can serve as valuable models for studying conditions such as osteogenesis imperfecta, where sulfation processes are implicated in disease mechanisms. In clinical settings, these knockout lines can aid in identifying potential therapeutic targets, and in the screening of drug candidates that may restore normal sulfation pathways.
What sets our PAPSS1 Gene Knockout Cell Lines apart from other genetic models is their high specificity and validated performance, ensuring reliable and reproducible results. Our cell lines are meticulously characterized and sourced from recognized standards, providing researchers with a baseline for experimental comparisons. The ready-to-use nature of our cell lines minimizes setup time and resource allocation, enabling faster progress in research projects.
For researchers and clinicians aiming to unravel the complexities of sulfate metabolism and its implications on health and disease, PAPSS1 Gene Knockout Cell Lines offer an essential and powerful tool. Our commitment to excellence in biological research products ensures you receive high-quality materials that are backed by extensive scientific expertise and support. Choose our PAPSS1 Gene Knockout Cell Lines to advance your research with confidence.
Please note that all services are for research use only. Not intended for any clinical use.
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