The ViraPower™ Adenoviral Promoterless Gateway™ Expression Kit combines Invitrogen’s ViraPower™ Adenoviral and Gateway™ technologies to facilitate easy recombination-based cloning and了解更多信息
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货号
数量
K494000
又称 K4940-00
1 kit
货号 K494000
又称 K4940-00
价格(CNY)
24,039.00
Each
添加至购物车
数量:
1 kit
价格(CNY)
24,039.00
Each
添加至购物车
The ViraPower™ Adenoviral Promoterless Gateway™ Expression Kit combines Invitrogen’s ViraPower™ Adenoviral and Gateway™ technologies to facilitate easy recombination-based cloning and adenoviral-based, transient expression of a target gene in dividing and non-dividing mammalian cells. The pAd⁄PL-DEST™ vector allows generation of an adenovirus containing the target gene where expression is driven by a promoter of choice. Alternatively, the vector may also be used to express small RNA molecules from their appropriate promoters.
Advantages • High efficiency and rapid recombination cloning • Produces high titer adenoviral stocks • Efficient delivery of the gene to dividing and non-dividing mammalian cells in vitro or in vivo • Allows gene of interest to be controlled by a promoter of choice • Produces replication-incompetent virus for enhanced biosafety of the system • Amenable for use in high-throughput applications
Key Features • Gateway™ Technology for efficient and rapid cloning • Promoterless vector that allows gene of interest to be controlled by a promoter of choice • Human Ad5 sequences (ΔE3) and Viral Inverted Terminal Repeats (ITRs) for packaging of the expression construct into virions • Ampicillin selection marker
Kit includes • pAd⁄PL-DEST™ Gateway™ Vector (6 μg. Cat. No. V493-20) • 293A Cell Line (3 x 106 cells, frozen. Cat. No. R705-07)
For research use only. Not intended for any therapeutic or diagnostic use.
仅供科研使用。不可用于诊断程序。
规格
构成或诱导系统组成型
输送类型腺病毒
适用于(应用)克隆您自己的启动子,病毒表达
产品类型Adenoviral Expression Kit
数量1 kit
载体pAd
克隆方法Gateway
产品线Gateway, ViraPower
促进剂None (Promoterless)
蛋白标记Untagged
Unit SizeEach
内容与储存
• pAd/PL-DEST Gateway™ Vector (Store at -20°C) • 293A Cell Line (Store in liquid nitrogen)
常见问题解答 (FAQ)
可以使用BP Clonase酶和LR Clonase酶替代BP Clonase II 酶LR Clonase II酶进行BP/LR Clonase反应的一步法实验方案吗?
在BP/LR Clonase反应的一步法实验方案中,不建议用BP Clonase酶和LR Clonase酶替代BP Clonase II 酶/LR Clonase II酶,因为这样的重组效率非常低。
Depletion of Chk1 leads to premature activation of Cdc2-cyclin B and mitotic catastrophe.
Authors:Niida H, Tsuge S, Katsuno Y, Konishi A, Takeda N, Nakanishi M,
Journal:J Biol Chem
PubMed ID:16159883
Mitotic catastrophe occurs as a result of the uncoupling of the onset of mitosis from the completion of DNA replication, but precisely how the ensuing lethality is regulated or what signals are involved is largely unknown. We demonstrate here the essential role of the ATM/ATR-p53 pathway in mitotic catastrophe from ... More