Gene: DRAM1
Official Full Name: DNA damage regulated autophagy modulator 1provided by HGNC
Gene Summary: This gene is regulated as part of the p53 tumor suppressor pathway. The gene encodes a lysosomal membrane protein that is required for the induction of autophagy by the pathway. Decreased transcriptional expression of this gene is associated with various tumors. This gene has a pseudogene on chromosome 4. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO18164 | DRAM1 Knockout cell line (HeLa) | Human | DRAM1 | 1:3~1:6 | Negative | Online Inquiry |
KO18165 | DRAM1 Knockout cell line (HCT 116) | Human | DRAM1 | 1:2~1:4 | Negative | Online Inquiry |
KO18166 | DRAM1 Knockout cell line (HEK293) | Human | DRAM1 | 1:3~1:6 | Negative | Online Inquiry |
KO18167 | DRAM1 Knockout cell line (A549) | Human | DRAM1 | 1:3~1:4 | Negative | Online Inquiry |
DRAM1 Gene Knockout Cell Lines are specifically engineered cellular models that feature the targeted deletion of the DNA damage-regulated autophagy modulator 1 (DRAM1) gene. This gene plays a critical role in autophagy and cellular responses to stress, particularly in the context of DNA damage. By utilizing CRISPR-Cas9 technology, these cell lines allow researchers to investigate the functional implications of DRAM1 deficiency, thereby unraveling the complex mechanisms of autophagy regulation and its downstream effects on cellular homeostasis and survival.
The primary function of these knockout cell lines lies in their ability to mimic pathophysiological conditions where DRAM1 is aberrant, offering a platform to study the gene's role in essential processes such as apoptosis, cell proliferation, and response to oncogenic stress. Researchers can use these cell lines to elucidate how the loss of DRAM1 influences cellular pathways, particularly those related to cancer development and progression, as well as neurodegenerative diseases, thus providing significant insights into potential therapeutic targets.
In clinical and research settings, DRAM1 Gene Knockout Cell Lines are invaluable for understanding the multifaceted roles of autophagy in health and disease. Their application ranges from basic research in molecular biology to preclinical studies aimed at developing novel cancer therapies. Compared to traditional stable cell lines, these knockout models offer enhanced specificity and reproducibility for studying the direct effects of gene knockout, minimizing off-target effects commonly observed with pharmacological inhibitors.
The distinct advantage of using DRAM1 knockout cell lines is underscored by their ability to enable high-throughput screening for chemical compounds or genetic modifiers that can restore autophagic processes or sensitize cells to chemotherapeutic agents. By bridging gaps in understanding the DRAM1 pathway, these models assist researchers and clinicians in advancing personalized medicine strategies.
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