- 询价
- 辰辉创聚生物®️
- NBST-248269
- 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 FAM72B Cell Line
货号：NBST-248269
品牌：辰辉创聚生物®️
规格：5x10^6 cells per vial
| 产品描述
NebuTools™ Human FAM72B Cell Line (Cat# NBST-248269) is generated by constitutive overexpression of the human FAM72B 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：FAM72B
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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文献和实验FAM caspase 8 and 9 binding assay for embryos
The FAM caspase binding assay kits from ATCC Corporation can be used to determine amounts of active caspases in cells. The FAM-labeled caspase inhibitor can freely diffuse into the cell. Active caspase irreversibly binds the inhibitor.
Online Verification of Human Cell Line Identity by STR DNA Typing
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
再获新进展！Mol Cell：施一公团队完善人类剪接体结构「地图」，揭示外显子连接机制
真核生物细胞中，基因编码区（exon）由内含子（intron）隔断，在转录翻译过程中，内含子需要经过 pre-mRNA 剪接来去除。RNA 剪接是真核生物「中心法则」的关键步骤之一，是蛋白质多样性、复杂性的分子基础。RNA 剪接体缺陷是导致人类疾病的重要原因之一，据估计可能超过 60% 的疾病与 Pre-mRNA 剪接有关。[1,2] 西湖大学施一公课题组十多年来聚焦酵母及人源剪接体结构解析及分子机制研究，取得了丰硕的成果。其中包括 10 篇 Science、4 篇 Cell、1 篇
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