Gene: MBNL2
Official Full Name: muscleblind like splicing regulator 2provided by HGNC
Gene Summary: This gene is a member of the muscleblind protein family which was initially described in Drosophila melanogaster. This gene encodes a C3H-type zinc finger protein that modulates alternative splicing of pre-mRNAs. Muscleblind proteins bind specifically to expanded dsCUG RNA but not to normal size CUG repeats and may thereby play a role in the pathophysiology of myotonic dystrophy. Several alternatively spliced transcript variants have been described but the full-length natures of only some have been determined. [provided by RefSeq, Mar 2012]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00144 | MBNL2 Knockout cell line (Vips) | Human | MBNL2 | Negative | Online Inquiry | |
KO32232 | MBNL2 Knockout cell line (HeLa) | Human | MBNL2 | 1:3~1:6 | Negative | Online Inquiry |
KO32233 | MBNL2 Knockout cell line (HCT 116) | Human | MBNL2 | 1:2~1:4 | Negative | Online Inquiry |
KO32234 | MBNL2 Knockout cell line (HEK293) | Human | MBNL2 | 1:3~1:6 | Negative | Online Inquiry |
KO32235 | MBNL2 Knockout cell line (A549) | Human | MBNL2 | 1:3~1:4 | Negative | Online Inquiry |
MBNL2 Gene Knockout Cell Lines are engineered cellular models designed to facilitate the study of the MBNL2 (muscleblind-like splicing regulator 2) gene, which is crucial in various biological processes including RNA splicing and development. These genetically modified cell lines enable researchers to explore the functional consequences of MBNL2 deficiency, providing insights into its role in pathological conditions such as myotonic dystrophy and other splicing-related disorders.
The key mechanism of MBNL2 knockout cell lines involves the targeted deletion of the MBNL2 gene using advanced genome-editing techniques, such as CRISPR-Cas9. By removing MBNL2, researchers can investigate the downstream effects on gene expression, alternative splicing events, and the overall cellular phenotype. This range of applications is vital for understanding the underlying molecular mechanisms of diseases linked to mis-splicing and aberrant gene regulation.
Scientifically, MBNL2 gene knockout cell lines are invaluable tools for both fundamental research and translational studies. They facilitate the development of potential therapeutic strategies aimed at correcting splicing defects and offer a platform for drug screening and validation. Compared to other models, these knockout cell lines provide a more accurate representation of the gene's loss-of-function effects, thus enhancing the reliability of experimental data.
One of the primary advantages of our MBNL2 knockout cell lines is their versatility; they can be used in various applications, including gene expression studies, drug target validation, and mechanisms underlying disease progression. Their reproducibility and reliability ensure that researchers can achieve consistent results, thereby enhancing the overall quality of their work.
For researchers, clinicians, and the biomedical community, investing in MBNL2 gene knockout cell lines is a strategic decision that could accelerate discoveries in the field of gene regulation and splicing disorders. With an unwavering commitment to quality and innovation, our company specializes in developing advanced biological products that empower scientific discovery and translational medicine.
Please note that all services are for research use only. Not intended for any clinical use.
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