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重要文件

EMU001571

Sigma-Aldrich

MISSION® esiRNA

targeting mouse Rasa2

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About This Item

分類程式碼代碼:
41105324
NACRES:
NA.51

描述

Powered by Eupheria Biotech

產品線

MISSION®

形狀

lyophilized powder

esiRNA cDNA 標靶序列

TTCCTTTCATCAAGCCTGGTACTTGCTACAGCCAAGAGACAATGGAAACAAATCATCTAAAACCGATGACCTGGGATCTCTTCTGTTAACTCTCTGCTATACAGAAGACTGCGTGCTTCCATCAGAGTACTATGGACCGCTGAAAACTTTGCTGCTAAAGTCACCAGATGTTCAGCCAGTATCCGCCTCAGCTGCTTATATTTTGGGTGAAATATGTCAAGATCAAAAGGATGCTGTTTTGCCCCTTGTACGACTGTTGCTGCATCACAATAAACTTGTCCCTTTTATCACTGCGGTGGCCGAGCTGGACTTGAAGGATACTCCAGATGCCAACGCAATATTTAGAGGAAACTCCCTGGCTACCCAGTGTCTGACTGAGATGATGAAGATAGTGGGAGGGCAC

Ensembl | 小鼠類登錄號

ENSMUSG00000032413

NCBI登錄號

NM_053268

運輸包裝

ambient

儲存溫度

−20°C

基因資訊

mouse ... RASA2(114713) , Rasa2(114713)

一般說明

MISSION® esiRNA are endoribonuclease prepared siRNA. They are a heterogeneous mixture of siRNA that all target the same mRNA sequence. These multiple silencing triggers lead to highly-specific and effective gene silencing.

For additional details as well as to view all available esiRNA options, please visit SigmaAldrich.com/esiRNA.

法律資訊

MISSION is a registered trademark of Merck KGaA, Darmstadt, Germany

儲存類別代碼

10 - Combustible liquids

閃點（°F）

Not applicable

閃點（°C）

Not applicable

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Peng-Chieh Chen et al.
Proceedings of the National Academy of Sciences of the United States of America, 111(31), 11473-11478 (2014-07-23)
Noonan syndrome (NS) is a relatively common genetic disorder, characterized by typical facies, short stature, developmental delay, and cardiac abnormalities. Known causative genes account for 70-80% of clinically diagnosed NS patients, but the genetic basis for the remaining 20-30% of

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