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一般說明
FBS仍然是一种常用的培养基补充剂，因为它在细胞培养中提供了广泛的功能。FBS提供营养、生长和附着因子，并通过难以在无血清培养基（SFM）系统中复制的机制保护细胞免受氧化损伤和细胞凋亡。
應用
胎牛血清在不同类型的细胞培养物中用作补充剂，例如：
该产品用于进一步的制造用途。本产品不用于人类或治疗用途。
- 在添加胎牛血清和其它成分的 Dulbecco ′改良 Eagle′培养基中PC12 细胞的生长。
- HeLa 细胞是在含有胎牛血清和其它成分的罗斯威尔公园纪念研究所 (RPMI) 1640 培养基中供养。
- BaF3 细胞培养物（细胞在补充胎牛血清和其它成分的 RPMI 1640 培养基中供养）。
- 原代海马细胞培养物（细胞在补充有热灭活胎牛血清和其它成分的Eagle′最低必需培养基供养）。
- HeLa、Cos1 和 Cos7 细胞在含有胎牛血清和其它成分的 Dulbecco 改良 Eagle 培养基 （DMEM） 中培养。
该产品用于进一步的制造用途。本产品不用于人类或治疗用途。
分析報告
- 内毒素和血红蛋白测试
- 检测了是否存在细菌、病毒和支原体
- 在无菌条件下用0.1微米膜过滤三次
儲存類別代碼
10 - Combustible liquids
水污染物質分類（WGK）
WGK 3
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves
R J Mark et al.
Journal of neurochemistry, 68(1), 255-264 (1997-01-01)
Peroxidation of membrane lipids results in release of the aldehyde 4-hydroxynonenal (HNE), which is known to conjugate to specific amino acids of proteins and may alter their function. Because accumulating data indicate that free radicals mediate injury and death of
Joseph E Rabinowitz et al.
Journal of virology, 76(2), 791-801 (2001-12-26)
The serotypes of adeno-associated virus (AAV) have the potential to become important resources for clinical gene therapy. In an effort to compare the role of serotype-specific virion shells on vector transduction, we cloned each of the serotype capsid coding domains
Julie L Webb et al.
The Journal of biological chemistry, 278(27), 25009-25013 (2003-04-30)
Parkinson's disease (PD) is characterized by the loss of dopaminergic neurons in the substantia nigra and the formation of aggregates (Lewy bodies) in neurons. alpha-Synuclein is the major protein in Lewy bodies and rare mutations in alpha-synuclein cause early-onset PD.
Maria C Cuitiño et al.
Cell reports, 27(12), 3547-3560 (2019-05-28)
Orchestrating cell-cycle-dependent mRNA oscillations is critical to cell proliferation in multicellular organisms. Even though our understanding of cell-cycle-regulated transcription has improved significantly over the last three decades, the mechanisms remain untested in vivo. Unbiased transcriptomic profiling of G0, G1-S, and S-G2-M
Tadepally Lakshmikanth et al.
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The human immune system varies extensively between individuals, but variation within individuals over time has not been well characterized. Systems-level analyses allow for simultaneous quantification of many interacting immune system components and the inference of global regulatory principles. Here, we
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