跳转至内容
Merck
CN

ESG1107

ESGRO®重组小鼠LIF蛋白

ESGRO Leukemia Inhibitory Factor (LIF) supplement for mouse ES cell culture. Each vial contains 10^7 units/ml.

别名:

Mouse LIF, Mouse Leukemia Inhibitory Factor, Murine LIF, Murine LIF, Mouse LIF, mLIF, mLIF

登录 查看组织和合同定价。

选择尺寸

变更视图

关于此项目

UNSPSC Code:
12352202
NACRES:
NA.75
eCl@ss:
32160801
Form:
liquid
Assay:
>95% (active component mLIF, SDS-PAGE)
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助


Quality Level

assay

>95% (active component mLIF, SDS-PAGE)

form

liquid

manufacturer/tradename

Chemicon®

concentration

10000000 units/mL

technique(s)

cell culture | stem cell: suitable

input

sample type induced pluripotent stem cell(s)
sample type: mouse embryonic stem cell(s)

NCBI accession no.

UniProt accession no.

shipped in

wet ice

storage temp.

2-8°C

Gene Information

mouse ... LIF(16878)

General description

ESGRO 小鼠 LIF 培养基补充剂以有效单位/mL 的形式提供,以确保批次之间的性能一致。 每批 ESGRO 补充剂均经过严格的质量控制测试,以确保能可靠地抑制小鼠多能干细胞分化。 ESGRO 小鼠 LIF 补充剂可用于小鼠胚胎干(ES)和诱导性多能干(iPS)细胞的基于饲养层和无饲养层的培养。
小鼠白血病抑制因子(LIF,mLIF)通过抑制自发分化,促进多能小鼠胚胎干(ES)和诱导多能干(iPS)细胞的自我更新和长期维持。

Application

ESGRO 补充剂的应用包括用作体外维持鼠 ES 细胞多能表型的试剂。

建议的实验方案:

ES 细胞:在 D3 和 MBL-1 多能 ES 细胞培养物中,研究发现,通常每 1.0 mL 组织培养基需要 1000 U ESGRO 补充剂来维持具有干细胞表型的 ES 细胞。 相似浓度的 mLIF 也已用于遗传修饰的 ES 细胞的种系传递(E3)。

在推荐浓度下,107 单位的 ESGRO 足以用于 10.0 L 的组织培养基,而 106 单位的 ESGRO 补充剂足以用于 1.0 L 的组织培养基。

Physical form

ESGRO 补充剂以液体形式提供,含量为 107 单位,溶于 1.0 mL 磷酸盐缓冲盐水,含 1%w/v 牛血清白蛋白 BSA 为载体以确保稳定性。
形式:纯化

Preparation Note

ESGRO 补充剂在环境温度下运输。出于客户关系,可能包含一个冰袋,但确实没必要。开发期间已使用 ESGRO 补充剂进行了广泛的稳定性测试。 该产品自生产之日起,以浓缩形式或在无菌组织培养基中稀释后至少可稳定保存 18 个月,且对 ES 细胞没有活性损失。 若要长期储存,建议将 ESGRO 补充剂储存于 4°C。 冻融会降低效力。建议在使用前,将 ESGRO 补充剂在无菌组织培养基中稀释并等分至合适的浓度,然后储存于 4°C。应避免冻融。在 ES 细胞培养期间,该产品在 37°C,5% CO2 培养箱中可稳定至少 7 天。
提供的 ESGRO® 补充剂经 0.22 微米无菌过滤,并在支原体检测中呈阴性。

Analysis Note

比活度:ESGRO® 补充剂在小鼠胚胎干细胞(D3 & MBL-1)和鼠 M1 髓样白血病细胞上进行了评估(4)。50 单位的标准定义为在 1.0mL 组织培养基中可诱导 50% 的 M1 菌落分化的 ESGRO 补充剂的浓度(4)。 10E7 单位相当于大约 100 μg 的纯蛋白质,足以处理 10L 的 ES 细胞培养基。

胚胎干细胞测定:分化抑制测定,浓度为 1000 单位/mL 小鼠骨髓白血病细胞 M1:比活度 >/= 108 单位/mg

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany
ESGRO is a registered trademark of Merck KGaA, Darmstadt, Germany


Still not finding the right product?

Explore all of our products under ESGRO®重组小鼠LIF蛋白


存储类别

12 - Non Combustible Liquids

flash_point_f

Not applicable

flash_point_c

Not applicable



分析证书(COA)

输入产品批号来搜索 分析证书(COA) 。批号可以在产品标签上"批“ (Lot或Batch)字后找到。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库


实验方案

Stem Cell protocols for cryopreservation, thawing of cryopreserved stem cells and media preparation.

商品

Leukemia Inhibitory Factor (LIF) is a stem cell growth factor used for the in vitro culture of pluripotent mouse embryonic stem cells (ES cells).

Naive pluripotent stem cells cultured in vitro using specialized media and inhibitors mimic "ground-state" cells from blastocysts.

Read types of stem cells including multipotent stem cells, Pluripotent stem cells and iPSCs and their applications in basic stem cell research, stem cell therapy and disease modelling

相关内容

Millipore’s new STEMCCA lentivirus reprogramming kits make it easier than ever to generate induced pluripotent stem (iPS) cells. Unlike traditional iPS generation which requires simultaneous co-infection by four separate expression vectors, the STEMCCA kits use a single polycistronic lentiviral vector to improve efficiency and reduce the number of viral integrations. The STEMCCA vector is comprised of the transcription factors Oct-4, Klf4, SOX-2, and c-Myc (OKSM), separated by the self-cleaving 2A peptide and IRES sequences 1,2. It is also available with flanking LoxP sites incorporated for Cre-mediated excision of the exogenous reprogramming transgenes. STEMCCA Vector Advantages: (1) Efficient: uses a single vector with four transcription factors rather than co-transducing four separate expression vectors (2) Minimizes viral integrations: single vector reduces the risks of insertional mutagenesis and viral reactivation and (3) Excisable: Cre/LoxP-regulated version enables removal of reprogramming transgenes.

查看所有相关内容

Isolation and characterization of neural crest-derived stem cells from dental pulp of neonatal mice.
Janebodin, Kajohnkiart, et al.
Testing, 6, e27526-e27526 (2011)
Novel hyperactive transposons for genetic modification of induced pluripotent and adult stem cells: a nonviral paradigm for coaxed differentiation.
Belay, Eyayu, et al.
Stem Cells, 28, 1760-1771 (2010)
Zhonghan Li et al.
Nature communications, 3, 1085-1085 (2012-09-27)
Somatic cells can be reprogrammed to form embryonic stem cell-like induced pluripotent stem cells (iPSCs), but the process suffers from low efficiency and the underlying molecular mechanisms that control reprogramming remain poorly understood. Here we perform an inhibitor screen to



全球贸易项目编号

货号GTIN
ESG110708436037124310