Gene: PLEKHM1
Official Full Name: pleckstrin homology and RUN domain containing M1provided by HGNC
Gene Summary: The protein encoded by this gene is essential for bone resorption, and may play a critical role in vesicular transport in the osteoclast. Mutations in this gene are associated with autosomal recessive osteopetrosis type 6 (OPTB6). Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Sep 2009]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO32672 | PLEKHM1 Knockout cell line (HeLa) | Human | PLEKHM1 | 1:3~1:6 | Negative | Online Inquiry |
KO32673 | PLEKHM1 Knockout cell line (HCT 116) | Human | PLEKHM1 | 1:2~1:4 | Negative | Online Inquiry |
KO32674 | PLEKHM1 Knockout cell line (HEK293) | Human | PLEKHM1 | 1:3~1:6 | Negative | Online Inquiry |
KO32675 | PLEKHM1 Knockout cell line (A549) | Human | PLEKHM1 | 1:3~1:4 | Negative | Online Inquiry |
PLEKHM1 Gene Knockout Cell Lines are genetically modified cell lines wherein the PLEKHM1 gene has been targeted and disrupted to elucidate its function and impact within biological systems. This gene encodes a protein that plays a crucial role in intracellular transport and secretion processes, particularly in the context of lysosomal function and cell signaling pathways. By creating knockout models, researchers can investigate the physiological and pathological roles of PLEKHM1, providing invaluable insights into diverse biological processes.
The primary mechanism by which PLEKHM1 Gene Knockout Cell Lines function is through the complete abrogation of the PLEKHM1 protein, which allows for the study of cellular responses and compensatory mechanisms induced by its absence. This is particularly relevant for understanding diseases linked to lysosomal dysfunction, such as neurodegenerative diseases and certain genetic disorders. In research contexts, these knockout cell lines facilitate the exploration of the gene’s role in various cellular activities, including autophagy, endocytosis, and immune responses.
The scientific importance of utilizing PLEKHM1 Gene Knockout Cell Lines extends to both basic research and clinical application. Mainly, they serve as a model for drug discovery and therapeutic development by enabling researchers to screen for novel compounds that target pathways associated with PLEKHM1. Moreover, the availability of these cell lines can accelerate the identification of biomarkers and therapeutic targets relevant to conditions in which PLEKHM1 is implicated.
Compared to other gene knockout models, PLEKHM1 Gene Knockout Cell Lines offer specific advantages, including validated stability, reproducibility, and seamless integration into existing experimental workflows. The specificity of the knockout allows researchers to obtain clearer, more definitive results, which is often a challenge with partial knockdowns or non-targeted approaches.
For researchers and clinicians alike, the value of PLEKHM1 Gene Knockout Cell Lines lies in their ability to provide decisive evidence on the biological functions of PLEKHM1 and its alteration in disease states. Our company specializes in the production and characterization of genetically modified cell lines, ensuring reliable and high-quality products that support pioneering research. By leveraging cutting-edge genetic engineering techniques, we commit to providing tools that empower advancements in the life sciences field.
Please note that all services are for research use only. Not intended for any clinical use.
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