Gene: LHFPL2
Official Full Name: LHFPL tetraspan subfamily member 2provided by HGNC
Gene Summary: This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in one LHFP-like gene result in deafness in humans and mice, and a second LHFP-like gene is fused to a high-mobility group gene in a translocation-associated lipoma. Alternatively spliced transcript variants have been found, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO32183 | LHFPL2 Knockout cell line (HeLa) | Human | LHFPL2 | 1:3~1:6 | Negative | Online Inquiry |
KO32184 | LHFPL2 Knockout cell line (HCT 116) | Human | LHFPL2 | 1:2~1:4 | Negative | Online Inquiry |
KO32185 | LHFPL2 Knockout cell line (HEK293) | Human | LHFPL2 | 1:3~1:6 | Negative | Online Inquiry |
KO32186 | LHFPL2 Knockout cell line (A549) | Human | LHFPL2 | 1:3~1:4 | Negative | Online Inquiry |
LHFPL2 Gene Knockout Cell Lines represent a cutting-edge tool in genetic research, specifically designed for the study of the LHFPL2 gene, which is implicated in various cellular processes, including cell adhesion, signaling, and differentiation. These cell lines are engineered to lack functional copies of the LHFPL2 gene, enabling researchers to investigate its role in physiological and pathological contexts by observing the cellular and molecular changes that occur in its absence.
The key functions of these cell lines encompass a broad spectrum of investigations into gene function, signal transduction pathways, and cellular behavior. By utilizing CRISPR/Cas9 technology for precise gene editing, these knockout lines facilitate robust experimentation, allowing for the dissection of gene interactions and the modeling of diseases linked to LHFPL2 dysregulation. Ultimate insights can be gained regarding cellular responses, including alterations in growth patterns, apoptosis, and immune responses.
The scientific importance of LHFPL2 Gene Knockout Cell Lines extends to both basic research and clinical applications. In biomedical studies, these lines can be used to model neurological disorders, providing a platform for drug development and therapeutic strategies. They can also serve as valuable resources for understanding tissue development and regenerative medicine.
Compared to traditional methods of gene disruption, such as homologous recombination or RNA interference, LHFPL2 Gene Knockout Cell Lines offer several advantages, including higher specificity, reduced off-target effects, and the ability to create stable mutations in a more streamlined manner. This advancement ensures that researchers obtain reliable and reproducible data, essential for furthering scientific knowledge.
For researchers and clinicians looking to deepen their understanding of LHFPL2's role in human health and disease, these knockout cell lines are an invaluable asset. They empower users to explore novel therapeutic avenues and elucidate complex biological mechanisms with confidence.
Our company stands at the forefront of genetic research innovation, providing high-quality biological products that enable groundbreaking discoveries. With extensive experience in gene editing technologies, we are committed to supporting the scientific community through our robust offerings, including the LHFPL2 Gene Knockout Cell Lines.
Please note that all services are for research use only. Not intended for any clinical use.
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