Gene: IMMP2L
Official Full Name: inner mitochondrial membrane peptidase subunit 2provided by HGNC
Gene Summary: This gene encodes a protein involved in processing the signal peptide sequences used to direct mitochondrial proteins to the mitochondria. The encoded protein resides in the mitochondria and is one of the necessary proteins for the catalytic activity of the mitochondrial inner membrane peptidase (IMP) complex. Two variants that encode the same protein have been described for this gene. [provided by RefSeq, Sep 2011]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00427 | IMMP2L Knockout cell line (HEK293) | Human | IMMP2L | 1:3~1:6 | Negative | Online Inquiry |
KO25290 | IMMP2L Knockout cell line (HeLa) | Human | IMMP2L | 1:3~1:6 | Negative | Online Inquiry |
KO25291 | IMMP2L Knockout cell line (HCT 116) | Human | IMMP2L | 1:2~1:4 | Negative | Online Inquiry |
KO25292 | IMMP2L Knockout cell line (A549) | Human | IMMP2L | 1:3~1:4 | Negative | Online Inquiry |
IMMP2L Gene Knockout Cell Lines are genetically engineered cell lines where the IMMP2L gene has been specifically targeted and disrupted to study its role in cellular processes and disease mechanisms. The IMMP2L gene encodes for an integral membrane protein that is believed to be involved in mitochondrial function and protein regulation within the cell. By utilizing CRISPR-Cas9 gene editing technology, these cell lines provide a powerful tool for researchers to investigate the functional consequences of IMMP2L loss and its implications in various biological pathways.
The key function of IMMP2L Gene Knockout Cell Lines lies in their ability to emulate the gene's absence, allowing researchers to monitor biochemical alterations, changes in signaling pathways, and cellular behavior typically influenced by the presence of this gene. Furthermore, these knockout cell lines serve as a critical mechanism to elucidate correlations between IMMP2L and various diseases, such as neurodegenerative conditions where mitochondrial dysfunction plays a prominent role.
Scientifically, IMMP2L Gene Knockout Cell Lines hold substantial importance for both basic and translational research. They can be invaluable for drug discovery, biomarker identification, and understanding the pathophysiology of disorders where the IMMP2L gene may be implicated. Their ability to facilitate assays related to mitochondrial function, cellular metabolism, and apoptosis positions them as a vital asset in research laboratories and clinical investigations.
Among the advantages of using IMMP2L Gene Knockout Cell Lines is their precise and reliable genetic modification, which mitigates the variability typically associated with natural cell lines. Unlike other knockout models that may introduce off-target effects or require complex validation, these cell lines provide researchers with a streamlined approach to study specific gene functions effectively.
The investment in IMMP2L Gene Knockout Cell Lines translates to significant value for researchers, clinicians, and pharmaceutical developers aiming to drive forward innovative therapies and research paradigms. As an advanced offering from our company, which specializes in high-quality biological products and genetic engineering technologies, we ensure that our cell lines are rigorously verified for accuracy and reproducibility, thus empowering our clients to achieve their research ambitions more efficiently.
Please note that all services are for research use only. Not intended for any clinical use.
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