- ￥10266
- Lifeline Cell Technology
- 美国
- FC-0046
- 2026年01月20日
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- 详细信息
- 文献和实验
- 技术资料
- 英文名：
Normal Human Lung Smooth Muscle Cells
- 细胞类型：
人正常原代细胞
- 物种来源：
人源
- 器官来源：
人源
- 运输方式：
干冰或液氮
- 年限：
液氮储存10年以上
- 生长状态：
冻存
- 规格：
500,000 cells/vial
Product Description
Lifeline® normal Human Lung Smooth Muscle Cells, when grown in VascuLife® SMC Medium, provide an ideal culture model for the study of angiogenesis, atherosclerosis, diabetes or vascular/pulmonary biology.
Lifeline® Lung Smooth Muscle Cells are cryopreserved as primary cells to ensure the highest viability, purity and plating efficiency.
- The cells have been isolated from human lung, plated and expanded in culture vessels once before being harvested for cryopreservation.
Lung smooth muscle cells immunostained for smooth muscle a-actin (red), nuclei stained with Hoechst (blue)
Our Human Lung Smooth Muscle Cells are quality tested in VascuLife® SMC Medium and demonstrate optimal low serum growth over a period of at least 15 population doublings at rates equal to or greater than other serum-supplemented media.
- Lung smooth muscle cells can be grown without phenol red or antimicrobials when cultured in VascuLife® SMC Medium.
Lifeline® human smooth muscle cells are not exposed to antimicrobials or phenol red when cultured in VascuLife® SMC Medium, an advantage since these supplements can cause cell stress and “masking effects” that may negatively impact experimental results. Lifeline® offers these traditional supplements; however, they are not needed, or recommended, to achieve optimal cell performance in most research applications.
500,000 cells per vial
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文献和实验Culture of Human Smooth Muscle Cells
The wall of a human artery consists of three distinct tunics. The tunica intima is lined by a layer of endothelial cells facing the lumen. Smooth muscle cells (SMCs) are the predominant cell type in the tunica media of arteries
Isolation and Culture of Human Airway Smooth Muscle Cells
cell. The study of smooth muscle cell immunobiology has been facilitated by the development of a technique for isolating and maintaining nontransformed human airway smooth muscle cells (1 ). These cells retain the physiologic responsiveness to a wide
Isolation, Culture, and Characterization of Human Intestinal Smooth Muscle Cells
and, over the course of 20 yr, have refined techniques for the isolation, culture, and characterization of smooth muscle cells of the human intestinal muscularis propria (1 ). These methodologies have been adapted for isolation of similar cell types from liver
