Gene: ADRA1D
Official Full Name: adrenoceptor alpha 1Dprovided by HGNC
Gene Summary: Alpha-1-adrenergic receptors (alpha-1-ARs) are members of the G protein-coupled receptor superfamily. They activate mitogenic responses and regulate growth and proliferation of many cells. There are 3 alpha-1-AR subtypes: alpha-1A, -1B and -1D, all of which signal through the Gq/11 family of G-proteins and different subtypes show different patterns of activation. This gene encodes alpha-1D-adrenergic receptor. Similar to alpha-1B-adrenergic receptor gene, this gene comprises 2 exons and a single intron that interrupts the coding region. [provided by RefSeq, Jul 2008]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO08082 | ADRA1D Knockout cell line (A549) | Human | ADRA1D | 1:3~1:4 | Negative | Online Inquiry |
ADRA1D Gene Knockout Cell Lines are specialized cellular models engineered to specifically disrupt the adrenergic receptor alpha-1D (ADRA1D) gene, which encodes a G protein-coupled receptor involved in various physiological processes, including smooth muscle contraction and neurotransmitter release. These cell lines are invaluable tools for researchers aiming to elucidate the molecular mechanisms underlying alpha-1D adrenergic signaling and its role in health and disease states.
The key function of ADRA1D Gene Knockout Cell Lines lies in their ability to simulate a loss-of-function scenario for the ADRA1D receptor, allowing for in-depth analysis of the receptor's biological pathways. Mechanistically, this knockout approach results in diminished responsiveness to adrenergic agonists, providing insights into receptor-mediated effects on pathways such as vasoconstriction, cardiovascular responses, and the modulation of neurogenic inflammation. Researchers can utilize these models to investigate the implications of ADRA1D signaling in conditions like hypertension, heart failure, and other cardiovascular disorders.
From a scientific perspective, the applications of these cell lines extend beyond basic research; they hold significant potential in drug discovery and therapeutic development. By employing ADRA1D knockout models, researchers gain valuable insights into receptor-specific signaling pathways, possibly informing clinical strategies to target dysregulated adrenergic signaling in various diseases.
A compelling advantage of the ADRA1D Gene Knockout Cell Lines is their specificity and reliability, providing a clearer understanding of alpha-1D receptor function compared to traditional approaches such as pharmacological blockade or overexpression systems. Additionally, these cell lines offer a streamlined experimental design, facilitating reproducibility and robust data generation that can considerably expedite research timelines.
For researchers and clinicians alike, the availability of ADRA1D Gene Knockout Cell Lines represents an essential resource for advancing our knowledge of adrenergic signaling pathways. The insights gained from these models can lead to innovative therapeutic strategies aimed at conditions linked with aberrant receptor function.
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