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Merck

SHC016

Sigma-Aldrich

MISSION® pLKO.1-puro 非靶 shRNA 对照质粒DNA

Targets no known genes from any species

别名:

MISSION® 对照载体, shRNA对照, 阴性shRNA对照, 阴性对照, 非靶shRNA, 非靶shRNA对照, 非靶对照

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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 pLKO.1-puro非靶标shRNA对照质粒DNA是一种慢病毒质粒载体。载体含有不靶向任何物种任何已知基因的shRNA(小发卡状RNA)插入片段,适合在使用MISSION shRNA文库克隆的实验中用作阴性对照。可用于检测转染的小发卡RNA对基因表达的影响,并解读shRNA克隆的敲低效应。氨苄青霉素和嘌呤霉素抗生素抗性基因分别用于细菌和哺乳动物细胞的选择性筛选。此外,利用表达载体与相容包装质粒共转染包装细胞(HEK293T),可生产自灭活复制缺陷病毒颗粒。非靶标shRNA对照质粒DNA产品为溶于Tris-EDTA(TE)缓冲液的500 ng/μl溶液,含有10 μg质粒DNA。

應用

MISSION® pLKO.1-puro非靶标shRNA对照质粒DNA已用作以下应用的转导对照:
  • 转导肿瘤细胞用于多色成像
  • 转导成人低钙诱导角质形成(HaCaT)细胞
  • 转导小鼠胚胎成纤维细胞,研究IP6K1(肌醇六磷酸激酶)的生物学功能
  • 研究星形胶质细胞分化中的Zac1(调节细胞凋亡和细胞周期阻滞的锌指蛋白)表达
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 2

閃點(°F)

Not applicable

閃點(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Zac1 regulates astroglial differentiation of neural stem cells through Socs3
Schmidt EU, et al.
Stem Cells, 31(8), 1621-1632 (2013)
Peroxiredoxin 2 nuclear levels are regulated by circadian clock synchronization in human keratinocytes
Avitabile D, et al.
The International Journal of Biochemistry & Cell Biology, 53(7580), 24-34 (2014)
Brain tumour cells interconnect to a functional and resistant network
Osswald M, et al.
Nature, 528(7580), 93-93 (2015)
Ryusuke Nakajima et al.
PloS one, 12(6), e0179585-e0179585 (2017-06-29)
A search for early response genes that are activated following germ cell induction from mouse embryonic stem cells in vitro led us to the isolation of a long noncoding RNA that contains a SINE (short interspersed element)-B1F motif that was
Sophie Weil et al.
Neuro-oncology, 19(10), 1316-1326 (2017-04-19)
Primary and adaptive resistance against chemo- and radiotherapy and local recurrence after surgery limit the benefits from these standard treatments in glioma patients. Recently we found that glioma cells can extend ultra-long membrane protrusions, "tumor microtubes" (TMs), for brain invasion

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