Gene: Ddr1
Official Full Name: discoidin domain receptor family, member 1provided by MGI
Gene Summary: Enables collagen binding activity. Involved in several processes, including regulation of extracellular matrix disassembly; smooth muscle cell-matrix adhesion; and wound healing, spreading of cells. Acts upstream of or within several processes, including collagen-activated tyrosine kinase receptor signaling pathway; mammary gland development; and neuron projection development. Located in plasma membrane. Is expressed in several structures, including central nervous system; future hindbrain; genitourinary system; mammary gland; and retina. Human ortholog(s) of this gene implicated in breast carcinoma; idiopathic pulmonary fibrosis; lung non-small cell carcinoma; osteosarcoma; and skin melanoma. Orthologous to human DDR1 (discoidin domain receptor tyrosine kinase 1). [provided by Alliance of Genome Resources, Apr 2025]
Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
---|---|---|---|---|---|---|
KO01360 | DDR1 Knockout cell line (HeLa) | Human | DDR1 | 1:3~1:6 | Negative | Online Inquiry |
KO05463 | DDR1 Knockout cell line (HCT 116) | Human | DDR1 | 1:2~1:4 | Negative | Online Inquiry |
KO05464 | DDR1 Knockout cell line (HEK293) | Human | DDR1 | 1:3~1:6 | Negative | Online Inquiry |
KO05465 | DDR1 Knockout cell line (A549) | Human | DDR1 | 1:3~1:4 | Negative | Online Inquiry |
Ddr1 Gene Knockout Cell Lines are genetically modified cell lines in which the Ddr1 (Discoidin domain receptor 1) gene has been inactivated or deleted. This product serves as a crucial tool for researchers investigating the role of Ddr1 in various biological processes. Under normal physiological conditions, Ddr1 is involved in cell adhesion, migration, and the modulation of cellular responses to the extracellular matrix, particularly in the context of fibrosis and tumor progression. By utilizing these knockout cell lines, scientists can elucidate the specific pathways and mechanisms through which Ddr1 contributes to cellular functions and disease states.
The key function of Ddr1 revolves around its receptor tyrosine kinase activity, which activates several downstream signaling cascades upon binding to collagen. The knockout of Ddr1 allows researchers to assess the resultant changes in cellular behavior, including altered proliferation, migration, and survival rates, providing insight into how Ddr1 might influence pathology in diseases such as cancer and fibrosis. As a result, these cell lines are invaluable in both basic research and potential therapeutic development.
The scientific importance of Ddr1 Gene Knockout Cell Lines extends to their application in drug screening, pathway analysis, and the development of targeted therapies aimed at modulating the effects of Ddr1 in pathological conditions. With the increasing relevance of personalized medicine, understanding the genetic profile of diseases at the molecular level, facilitated by these knockout lines, is critical for the advancement of clinical interventions.
What sets our Ddr1 Gene Knockout Cell Lines apart from alternatives is their reliable performance and stringent validation processes, ensuring that researchers work with high-quality models that accurately reflect the Ddr1 knockout phenotype. The ease of use in various experimental setups further enhances their accessibility to laboratories of all sizes.
Researchers and clinicians will find immense value in these cell lines as they pave the way for translational research and novel therapeutic approaches. By investing in understanding and manipulating the Ddr1 pathway, users can contribute to the fight against diseases with substantial fibroproliferative components.
At [Your Company Name], we specialize in providing cutting-edge biological research tools, backed by our team of experts dedicated to advancing scientific discovery. Our commitment to quality and innovation ensures that our products, such as the Ddr1 Gene Knockout Cell Lines, meet the evolving needs of the research community.
Please note that all services are for research use only. Not intended for any clinical use.
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