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Merck

SHC007

Sigma-Aldrich

MISSION® pLKO.1-puro 荧光素酶 shRNA 对照质粒 DNA

shRNA sequence targeting luciferase

别名:

MISSION® 对照载体

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About This Item

MDL號碼:
分類程式碼代碼:
41106609
NACRES:
NA.51

品質等級

產品線

MISSION®

濃度

500 ng/μL in TE buffer; DNA (10μg of plasmid DNA)

運輸包裝

dry ice

儲存溫度

−20°C

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一般說明

MISSION ® 荧光素酶 shRNA 对照载体是一个 7,091 碱基对的慢病毒质粒载体,含有靶向来自 Photinus pyralis 荧光素酶的 shRNA 序列(GenBank 登记号:M15077)。荧光素酶 shRNA 对照载体在使用表达萤火虫荧光素酶的细胞系的实验中作为阳性敲除对照十分有用。其也可作为阴性对照载体。

氨苄西林和嘌呤霉素抗生素抗性基因分别在细菌或哺乳动物细胞中提供选择。此外,通过与相容的包装质粒共转染,可在包装细胞 (HEK293T) 中产生自我失活复制无能的病毒颗粒,MISSION ® 慢病毒包装混合物(产品编号:SHP001)。荧光素酶 shRNA 对照载体以 10μg 质粒 DNA,溶于 Tris-EDTA (TE) 缓冲液中,浓度为 500 ng/μl.

應用

想要查看更多应用数据、实验方案和载体图谱,请访问 sigma.com/shrna

法律資訊

使用本产品需遵守一个或多个许可协议。有关详细信息,请参阅http://sigmaaldrich.com/missionlicense
MISSION is a registered trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Islands of spatially discordant APD alternans underlie arrhythmogenesis by promoting electrotonic dyssynchrony in models of fibrotic rat ventricular myocardium.
Majumder R
Scientific Reports, 6 (2016)
Ivana Horvathova et al.
Molecular cell, 68(3), 615-625 (2017-10-24)
RNA degradation plays a fundamental role in regulating gene expression. In order to characterize the spatiotemporal dynamics of RNA turnover in single cells, we developed a fluorescent biosensor based on dual-color, single-molecule RNA imaging that allows intact transcripts to be
Deepak Bararia et al.
Nature communications, 7, 10968-10968 (2016-03-24)
CCAAT/enhancer-binding protein alpha (C/EBPα) is an essential transcription factor for myeloid lineage commitment. Here we demonstrate that acetylation of C/EBPα at lysine residues K298 and K302, mediated at least in part by general control non-derepressible 5 (GCN5), impairs C/EBPα DNA-binding
Gundula Streubel et al.
Molecular cell, 70(2), 371-379 (2018-04-03)
The Polycomb repressor complex 2 (PRC2) is composed of the core subunits Ezh1/2, Suz12, and Eed, and it mediates all di- and tri-methylation of histone H3 at lysine 27 in higher eukaryotes. However, little is known about how the catalytic
The epigenetic regulators CBP and p300 facilitate leukemogenesis and represent therapeutic targets in acute myeloid leukemia.
Giotopoulos G
Oncogene, 35(3), 279-289 (2016)

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