Gene: LMBR1L
Official Full Name: limb development membrane protein 1 likeprovided by HGNC
Gene Summary: Enables transmembrane signaling receptor activity. Involved in receptor-mediated endocytosis and signal transduction. Located in endoplasmic reticulum membrane and plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO16519 | LMBR1L Knockout cell line (HeLa) | Human | LMBR1L | 1:3~1:6 | Negative | Online Inquiry |
KO16520 | LMBR1L Knockout cell line (HCT 116) | Human | LMBR1L | 1:2~1:4 | Negative | Online Inquiry |
KO16521 | LMBR1L Knockout cell line (HEK293) | Human | LMBR1L | 1:3~1:6 | Negative | Online Inquiry |
KO16522 | LMBR1L Knockout cell line (A549) | Human | LMBR1L | 1:3~1:4 | Negative | Online Inquiry |
LMBR1L Gene Knockout Cell Lines are genetically engineered cell lines that specifically lack the expression of the LMBR1L (Limb Development Membrane Protein 1-like) gene. These cell lines are invaluable tools in molecular biology and genetics research, enabling scientists to explore the role of the LMBR1L gene in various biological processes, including limb development, cellular signaling pathways, and disease mechanisms. By removing the expression of LMBR1L, researchers can study the resultant phenotypic changes and assess the gene's contribution to cellular functions.
The key function of LMBR1L Gene Knockout Cell Lines lies in their ability to facilitate targeted investigations into gene function through loss-of-function analysis. The knockout mechanism offers researchers a powerful tool to elucidate the significance of the LMBR1L gene in developmental biology and pathophysiology. This is crucial for identifying potential therapeutic targets for congenital abnormalities and other disorders associated with limb development.
Scientifically, these cell lines are significant for their applications in both research and clinical settings. They serve as critical models for studying genetic mutations, enabling researchers to better understand the loci associated with developmental disorders, raise awareness about the implications of gene interactions during limb development, and enhance drug discovery processes aimed at ameliorating related conditions.
What sets LMBR1L Gene Knockout Cell Lines apart from other cell models is their specificity and reliability in yielding consistent, reproducible results. Compared to alternative models, such as transient knockdowns or less specific knockouts, the stable expression of the knockout ensures that researchers are able to observe the full implications of LMBR1L gene loss over extended experimental durations.
For researchers and clinicians aiming to pioneer advancements in genetic understanding and therapeutic approaches, these cell lines represent an essential asset. By incorporating LMBR1L Gene Knockout Cell Lines into their studies, they can gain profound insights into gene functionality and related pathologies, ultimately contributing to targeted developments in clinical applications.
Our company possesses extensive expertise in genetic engineering, offering a suite of high-quality biological products designed to facilitate cutting-edge research. We are committed to providing tools that empower scientists to advance their understanding of genetics and its implications in health and disease.
Please note that all services are for research use only. Not intended for any clinical use.
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