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- 详细信息
- 文献和实验
- 技术资料
- 库存:
100
- 供应商:
上海酶研生物科技有限公司
- 英文名:
AdM (Adipocyte Medium)
- 规格:
500ml/T
|
货号 |
7201 |
|
产地 |
美国 |
|
缩写 |
AdM |
|
规格 |
500ml |
|
用途 |
科研 |
|
储存 |
4度,-20度 |
|
运输 |
胶冰 |
脂肪细胞培养基是为正常人类脂肪细胞体外培养设计的适于其生长的培养基。是经灭菌的液体培养基,包含所有培养脂肪细胞必需营养物质。该培养基缓冲体系为重碳酸盐,在含5%CO2的细胞培养箱中平衡后pH值为7.4。
脂肪细胞培养基包含500 ml基础培养基,12.5ml胎牛血清(FBS,目录编号0012),5m脂肪细胞生长添加物(AdGS,目录编号7262)和5 ml青霉素/链霉素溶液(P/S,目录编号0503)
19.) Liu Q, Hou J, Chen X, Liu G, Zhang D, Sun H, Zhang J. (2014) "P-Glycoprotein Mediated Efflux Limits the Transport of the Novel Anti-Parkinson's Disease Candidate Drug FLZ across the Physiological and PD Pathological In Vitro BBB Models."?PloS one. 9: e102442.
20.) Tong X, Lv P, Mathew AV, Liu D, Niu C, Wang Y, Ji L, Li J, Fu Z, Pan B, Pennathur S, Zheng L, Huang Y. (2014) "The compensatory enrichment of sphingosine-1-phosphate harbored on glycated high-density lipoprotein restores endothelial protective function in type 2 diabetes mellitus."?Cardiovascdiabetol. 13: 82.
21.) Umar MI, Asmawi MZ, Sadikun A, Majid AMSA, Al-Suede FSR, Hassan LEA, Altaf R, Ahamed MBK. (2014) "Ethyl-p-methoxycinnamate isolated from kaempferiagalanga inhibits inflammation by suppressing interleukin-1, tumor necrosis factor-&aplha;, and angiogenesis by blocking endothelial functions."?Clinics. 69: 134-44.
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文献和实验
19.) Liu Q, Hou J, Chen X, Liu G, Zhang D, Sun H, Zhang J. (2014) "P-Glycoprotein Mediated Efflux Limits the Transport of the Novel Anti-Parkinson's Disease Candidate Drug FLZ across the Physiological and PD Pathological In Vitro BBB Models."?PloS one. 9: e102442.
20.) Tong X, Lv P, Mathew AV, Liu D, Niu C, Wang Y, Ji L, Li J, Fu Z, Pan B, Pennathur S, Zheng L, Huang Y. (2014) "The compensatory enrichment of sphingosine-1-phosphate harbored on glycated high-density lipoprotein restores endothelial protective function in type 2 diabetes mellitus."?Cardiovascdiabetol. 13: 82.
21.) Umar MI, Asmawi MZ, Sadikun A, Majid AMSA, Al-Suede FSR, Hassan LEA, Altaf R, Ahamed MBK. (2014) "Ethyl-p-methoxycinnamate isolated from kaempferiagalanga inhibits inflammation by suppressing interleukin-1, tumor necrosis factor-&aplha;, and angiogenesis by blocking endothelial functions."?Clinics. 69: 134-44.
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