Merck

M9309

Sigma-Aldrich

McCoy 5A培养基

Modified, with L-glutamine and sodium bicarbonate, liquid, sterile-filtered, suitable for cell culture

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别名:
5A basal medium
MDL编号:

无菌性

sterile-filtered

形式

liquid

technique(s)

cell culture | mammalian: suitable

杂质

endotoxin, tested

组分

NaHCO3: 2.2 g/L
L-glutamine: 0.21 g/L
phenol red: 0.011 g/L
glucose: 3.0 g/L (Dextro)

运输

ambient

储存温度

2-8°C

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McCoy 5A培养基

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SAFC

SAFC

N1140

NCTC 109 Medium

form

liquid

form

liquid

form

liquid

form

liquid

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

impurities

endotoxin, tested

impurities

endotoxin, tested

impurities

Endotoxin, tested

impurities

endotoxin, tested

components

NaHCO3: 2.2 g/L
L-glutamine: 0.21 g/L
phenol red: 0.011 g/L
glucose: 3.0 g/L (Dextro)

components

phenol red: yes
sodium pyruvate: no
L-glutamine: no
HEPES: no
NaHCO3: yes
Earle’s salts (5% CO2): yes

components

glucose: 1.0 g/L
L-glutamine: 0.292 g/L
phenol red: 0.011 g/L
NaHCO3: 2.2 g/L

components

glucose: 1.0 g/L
phenol red: 0.02 g/L
L-glutamine: no
NaHCO3: 2.2 g/L

shipped in

ambient

shipped in

ambient

shipped in

ambient

shipped in

ambient

一般描述

McCoy 及其同事报道了体外培养 Novikoff 肝癌细胞所需的氨基酸。这些实验使用的是基础培养基 5A,该培养基后来被改良产生 McCoy′s 5A 培养基。

应用

McCoy′s 5A 培养基已用于:
  • 培养 HCT-116?细胞
  • 培养透明细胞肾细胞癌(ccRCC)细胞 Caki-1
  • 维持和培养人骨肉瘤 Saos-2 细胞系,用于体外细胞研究

生化/生理作用

McCoys 5A培养基起初是通过修改BME中的氨基酸,用来支持肝肿瘤细胞。 该配方还被用来支持骨髓、皮肤、牙龈、肾脏、大网膜、肾上腺、肺、脾、大鼠胚胎和其他细胞类型原代培养的生长。

储存分类代码

12 - Non Combustible Liquids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Aleksandr Ianevski et al.
Cancers, 12(6) (2020-07-08)
The evidence that pan-Bcl-2 or Bcl-xL-specific inhibitors prematurely kill virus-infected or RNA/DNA-transfected cells provides rationale for investigating these apoptotic inducers further. We hypothesized that not only invasive RNA or DNA (biological factors) but also DNA/RNA-damaging chemical or physical factors could
Alison Roth et al.
Nature communications, 9(1), 1837-1837 (2018-05-11)
Malaria liver stages represent an ideal therapeutic target with a bottleneck in parasite load and reduced clinical symptoms; however, current in vitro pre-erythrocytic (PE) models for Plasmodium vivax and P. falciparum lack the efficiency necessary for rapid identification and effective
Xiang-Ping Liu et al.
Journal of experimental & clinical cancer research : CR, 28, 52-52 (2009-04-21)
RhoA and RhoC are deregulated by over expression in many human tumors, including colorectal cancer. Some reports show that they play a pivotal role in the carcinogenesis, tumor development and infiltration metastasis. In this study, for the first time we
Nengquan Sheng et al.
Cancer medicine, 6(6), 1331-1340 (2017-04-26)
MicroRNA-145 (miR-145), as a tumor-suppressive miRNA, has been demonstrated down-regulated in colorectal cancer (CRC) cells, and could inhibit CRC cells growth. However, the molecular pathway in which miR-145 modulates CRC malignant transformation has not been fully revealed. Here, we reported
Qiao Zhang et al.
International journal of oncology, 57(1), 197-212 (2020-04-23)
Glucose‑6‑phosphate dehydrogenase (G6PD) is crucial rate‑limiting enzyme of the pentose phosphate pathway (PPP). G6PD dysregulation has been reported in various types of human cancer, and the role of G6PD in cancer progression was demonstrated in numerous studies. A previous study

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