推荐产品
生物来源
human coronary artery (normal, tunica intima and media)
质量水平
包装
pkg of 500,000 cells
制造商/商品名称
Cell Applications, Inc
生长模式
Adherent
核型
2n = 46
形态学
smooth muscle
技术
cell culture | mammalian: suitable
相关疾病
diabetes; stroke; cardiovascular diseases
运输
dry ice
相关类别
1 of 4
此商品 | A4414 | G2500 | C3400 |
---|---|---|---|
assay ≥70% protein basis (biuret) | assay ≥99% (agarose gel electrophoresis) | assay 70-90% (biuret) | assay 87-94% protein basis |
biological source Porcine muscle | biological source Porcine | biological source Porcine skin | biological source bovine milk |
technique(s) electrophoresis: suitable | technique(s) cell culture | mammalian: suitable | technique(s) cell culture | mammalian: suitable | technique(s) activity assay: suitable, electrophoresis: suitable, immunocytochemistry: suitable |
form lyophilized powder (contains Tris buffer salts) | form lyophilized powder | form powder | form powder |
storage temp. −20°C | storage temp. 2-8°C | storage temp. - | storage temp. - |
Quality Level 200 | Quality Level 200 | Quality Level 200 | Quality Level 200 |
一般描述
Human Coronary Artery Smooth Muscle Cells (HCASMC) provide an excellent model system to study all aspects of cardiovascular function and disease, especially those related to mechanisms of hyperplasia and hypertrophy of intimal smooth muscle cells leading to vascular occlusion in atherosclerosis and stent restenosis.
HCASMC has been utilized in a number of research studies, for example, to:
- Study signaling pathways regulating smooth muscle differentiation (Zhou, 2010); and chronic inflammation of arterial wall that leads to artherosclerosis (Kiyan, 2014)
- Demonstrate that STAT-1 and STAT-3 regulate VEGF production in smooth muscle cells by having opposing effects on HIF-1α expression (Albasanz-Puig, 2012); study the mechanisms of hypoxia and reoxigenation injuries in by demonstrating increased production of ROS and inflammatory cytokines, and further showing that DHA is not beneficial in this type of injuries (Feng, 2012)
- Investigate the gene expression differences between smooth muscle cells from different arteries, underlying their differential response to injuries and proliferation stimuli (Lange, 2013)
- Suggest the hypermethylation of SOCS3 gene as the connection between TNF-α and IGF-1 released in response to mechanical injury during coronary intervention, and the induction of cytokines leading to intimal hyperplasia and restenosis (Dhar, 2013)
- Develop a novel VEGFR/MET-targeted inhibitor with improved antitumor efficacy and decreased toxicity (Fujita, 2013); and investigate novel therapies and drug combinations to achieve optimal target selectivity (Lehar, 2009; Wo-Wong, 2013)
- Develop elastic scaffolds for tissue engineering (Nivison-Smith, 2010, 2012) and novel treatment strategies to prevent stent restenosis by designing new materials (Crowder, 2012), or drug therapies to preferentially inhibit smooth muscle cell growth (O’Neill, 2009; Mociornita, 2013)
Characterization: positive for smooth muscle cell specific alpha-actin expression.
细胞系来源
应用
组分
制备说明
- 2nd passage, >500,000 cells in Basal Medium containing 10% FBS & 10% DMSO
- Can be cultured at least 16 doublings
传代培养常规
免责声明
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
商品
Technical information for working with human coronary artery smooth muscle cells including thawing, subculturing and cryopreservation
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