Gene: AP2M1
Official Full Name: adaptor related protein complex 2 subunit mu 1provided by HGNC
Gene Summary: This gene encodes a subunit of the heterotetrameric coat assembly protein complex 2 (AP2), which belongs to the adaptor complexes medium subunits family. The encoded protein is required for the activity of a vacuolar ATPase, which is responsible for proton pumping occurring in the acidification of endosomes and lysosomes. The encoded protein may also play an important role in regulating the intracellular trafficking and function of CTLA-4 protein. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2015]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO00468 | AP2M1 Knockout cell line (A549) | Human | AP2M1 | 1:3~1:4 | Negative | Online Inquiry |
KO38531 | AP2M1 Knockout cell line (HeLa) | Human | AP2M1 | 1:3~1:6 | Negative | Online Inquiry |
KO38532 | AP2M1 Knockout cell line (HCT 116) | Human | AP2M1 | 1:2~1:4 | Negative | Online Inquiry |
KO38533 | AP2M1 Knockout cell line (HEK293) | Human | AP2M1 | 1:3~1:6 | Negative | Online Inquiry |
AP2M1 Gene Knockout Cell Lines represent a specialized tool in cellular and molecular biology that enables researchers to study the function of the AP2M1 gene, which encodes a subunit of the adaptor protein complex 2 (AP-2). This complex plays a crucial role in clathrin-mediated endocytosis, a fundamental cellular process that facilitates the internalization of membrane receptors and other extracellular materials. By employing CRISPR-Cas9 technology, these cell lines allow for the precise knockout of the AP2M1 gene, enabling the dissection of its role in various physiological and pathological contexts.
The primary function of the AP2M1 Gene Knockout Cell Lines is to facilitate the investigation of downstream signaling pathways and cellular processes influenced by the absence of AP2M1. Researchers can examine changes in receptor recycling, membrane trafficking, and cellular responses to stimuli or therapeutic interventions. Additionally, the lack of AP2M1 expression can illuminate the gene's implications in diseases such as cancer, neurodegenerative disorders, and infectious diseases, where endocytic pathways may be disrupted.
In terms of scientific importance, these cell lines offer unparalleled value in both research and clinical settings. They enable the development of novel therapeutic strategies by providing a platform to test the efficacy of drugs targeting endocytic pathways or to unravel disease mechanisms tied to AP2M1 dysfunction. Moreover, their utility extends to pharmaceutical industries interested in drug development pipelines where alternative expression systems may not yield the desired physiological relevance.
Compared to traditional methods, the AP2M1 Gene Knockout Cell Lines provide unique advantages by offering precise genetic alterations, reducing off-target effects associated with older techniques. This enhances reproducibility and validity of experimental results, making them a reliable resource for high-throughput studies and screening assays.
Researchers and clinicians can leverage these cell lines for impactful discoveries, validating hypotheses about AP2M1’s role in disease biology, and potentially identifying biomarkers for therapeutic responses. By choosing our AP2M1 Gene Knockout Cell Lines, professionals gain access to a robust research tool backed by our extensive expertise in cell line development and molecular biology. Our commitment to quality and innovation positions us as a leader in providing critical biological resources that empower advances in health and science.
Please note that all services are for research use only. Not intended for any clinical use.
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