描述
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产品线
MISSION®
表单
lyophilized powder
esiRNA cDNA靶序列
GGGATGGATTCACCATTCTGTCTTCTAAGAGCCTTGTTCTGGGACAGAAGCTGTCCTTAACCCAGAGTGACATCAGCCATATTGGCTCCATGAGAGTGGAGGGCATTGTCCACCCAACCACAGCCGAAATTGACCTCAAAGAAGATATAGGTAAAGCCTTGGAAAAGGCTGGGGGAAAAGAGTTCTTGGAAACGGTAAAGGAGCTTCGCAAATCCCAAGGCCCTTTGGAAGTCGCCGAAGCCGCCGTCAGCCAATCCAGTGGACTCGCAGCCAAATTTGTCATCCACTGTCACATCCCTCAGTGGGGCTCCGACAAATGTGAAGAACAGCTTGAAGAGACCATCAAAAACTGCCTGTCAGCGGCGGAGGACAAGAAGCTAAAGTCCGTCGCGTTCCCGCCTTTCCCCAGCGGCAGAAACTGCTTTCCCAAACAGACTGCGGCCCAGGTGACCCTCAAAGCCATCTCAGCCCACTTTGATGACTCGAGCGCGTCCTCGCTGAAGAACGTGTACTTCCTGCTCTTCGACAGC
基因组数据库 |人类登记号
NCBI登记号
运输
ambient
储存温度
−20°C
基因信息
human ... H2AFY2(55506), H2AFY2(55506)
一般描述
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.
For additional details as well as to view all available esiRNA options, please visit SigmaAldrich.com/esiRNA.
法律信息
MISSION is a registered trademark of Merck KGaA, Darmstadt, Germany
储存分类代码
10 - Combustible liquids
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
新产品
此项目有
Kai Ni et al.
Nature communications, 11(1), 5647-5647 (2020-11-08)
The human Immunodeficiency Centromeric Instability Facial Anomalies (ICF) 4 syndrome is a severe disease with increased mortality caused by mutation in the LSH gene. Although LSH belongs to a family of chromatin remodeling proteins, it remains unknown how LSH mediates
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