- 询价
- 辰辉创聚生物®️
- NBST-248081
- 2026年05月18日
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- 详细信息
- 文献和实验
- 技术资料
- 库存：
大量
- 供应商：
北京辰辉创聚生物技术有限公司
- 规格：
5x10^6 cells per vial
| 产品信息
品名：NebuTools™ Human FAM157B Cell Line
货号：NBST-248081
品牌：辰辉创聚生物®️
规格：5x10^6 cells per vial
| 产品描述
NebuTools™ Human FAM157B Cell Line (Cat# NBST-248081) is generated by constitutive overexpression of the human FAM157B gene via stable transfection. It exhibits sustained and reproducible expression of the target gene, and is suitable for in vitro functional studies, mechanistic research, and drug discovery or screening applications. Please feel free to contact us for technical details and supporting data.
| 产品属性
Species：Human
Gene：FAM157B
Host Cell：Stable cell lines are available across multiple cell types, including but not limited to HEK293, CHO, Jurkat, K562, Raji, HCT116, MC38, PANC-1, A549, A375, MDA-MB-231, L929, HepG2, and HeLa.
Stability：Validated for at least 10 passages
Quality Control：Negative for bacteria, yeast, fungi and mycoplasma.
Revival：After retrieving the cells from the liquid nitrogen tank, rapidly thaw them in a 37°C water bath. Transfer contents into a tube with pre-warmed media. Centrifuge cells and seed into a 25cm^2 flask containing pre-warmed media.
Applications：Widely used in mechanisms study, high-throughput screening, drug target validation and others.
Storage：Liquid nitrogen
Shipment：Dry Ice
For Research Use Only!
To get more information, please contact us freely.
郑重声明：仅用于科学研究，不可用于诊断及治疗。
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The main prerequisition for any research, development, or production programs involving cell lines is whether a cell line is authentic or not. Microsatellites in the human genome harboring short tandem repeat (STR) DNA markers allow
We document the protocols and methods for the production of immortalized cell lines of human neural stem cells from the human fetal central nervous system (CNS) cells by using a retroviral vector encoding v-myc oncogene. One of the human
Screening of compounds toxicity against human Monocytic cell line-THP-1 by flow cytometry
is human alveolar macrophages. Thus, evaluation of candidate drugs for macrophage toxicity is crucial. Protocols for high throughput drug toxicity screening of macrophages using flow cytometry are lacking in the literature. For this application we modified
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