Gene: FMR1
Official Full Name: fragile X messenger ribonucleoprotein 1provided by HGNC
Gene Summary: The protein encoded by this gene binds RNA and is associated with polysomes. The encoded protein may be involved in mRNA trafficking from the nucleus to the cytoplasm. A trinucleotide repeat (CGG) in the 5' UTR is normally found at 6-53 copies, but an expansion to 55-230 repeats is the cause of fragile X syndrome. Expansion of the trinucleotide repeat may also cause one form of premature ovarian failure (POF1). Multiple alternatively spliced transcript variants that encode different protein isoforms and which are located in different cellular locations have been described for this gene. [provided by RefSeq, May 2010]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00028 | FMR1 Knockout cell line (SH-SY5Y) | Human | FMR1 | 1:2-1:3 | Negative | Online Inquiry |
KO00372 | FMR1 Knockout cell line(293T) | Human | FMR1 | 1:3~1:6 | Negative | Online Inquiry |
KO02883 | FMR1 Knockout cell line (HeLa) | Human | FMR1 | 1:3~1:6 | Negative | Online Inquiry |
KO02884 | FMR1 Knockout cell line (HCT 116) | Human | FMR1 | 1:2~1:4 | Negative | Online Inquiry |
KO02885 | FMR1 Knockout cell line (HEK293) | Human | FMR1 | 1:3~1:6 | Negative | Online Inquiry |
KO02886 | FMR1 Knockout cell line (A549) | Human | FMR1 | 1:3~1:4 | Negative | Online Inquiry |
FMR1 Gene Knockout Cell Lines are specialized cell lines engineered to lack the Fragile X Mental Retardation 1 (FMR1) gene, which plays a crucial role in synaptic function and neural development. These knockout models are pivotal for studying Fragile X syndrome (FXS), the most common heritable form of intellectual disability, and they serve as a powerful tool in understanding the molecular mechanisms underlying various neurodevelopmental disorders.
The primary function of these cell lines is to facilitate investigations into the pathways affected by the absence of FMR1, which is known to be involved in mRNA translation and synaptic plasticity. By using FMR1 knockout cell lines, researchers can delve deeper into the dysfunctions that arise in neuronal signaling and connectivity, providing insights into the pathophysiology of FXS and related conditions. This empowers scientists to assess potential therapeutic interventions aimed at restoring normal cellular functions.
The scientific importance of FMR1 Gene Knockout Cell Lines extends beyond basic research; they are invaluable in preclinical studies for drug development and the evaluation of novel therapeutic strategies. Their ability to mimic the physiological conditions of FXS enables researchers to screen compounds that could enhance synaptic function or ameliorate cognitive deficits.
Compared to traditional cell models, FMR1 knockout cell lines offer distinct advantages, including precise genetic modification, consistent reproducibility, and the capability to assess complex biological processes in controlled environments. Their specificity for the FMR1 gene provides enhanced reliability for researchers seeking to make significant contributions to the field of neurobiology.
Ultimately, FMR1 Gene Knockout Cell Lines are a vital resource for researchers and clinicians focused on neurodevelopmental disorders. Their unique capabilities not only facilitate advanced scientific inquiry but also foster the development of targeted therapies that can improve patient outcomes. By choosing FMR1 Gene Knockout Cell Lines, you leverage our company’s extensive expertise in producing high-quality biological products, underpinned by rigorous research and development efforts that ensure the reliability and effectiveness of our offerings.
Please note that all services are for research use only. Not intended for any clinical use.
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