产品名称
MISSION® esiRNA, targeting human ATMIN
description
Powered by Eupheria Biotech
product line
MISSION®
form
lyophilized powder
esiRNA cDNA target sequence
GCCACTGCTGATTCCTCTGTGTCGTCTTGTTCTCAAACTGATTTGTCGTTTGATTCTCAAGTGTCTCTTCCCATTAGTGTTCACACTCAGACATTTTTGCCCAGCTCTAAGGTAACTTCATCTATAGCTGCTCAGACTGATGCATTTATGGACACCTGTTTCCAGTCAGGTGGGGTCTCCAGAGAAACTCAAACCAGTGGGATAGAAAGTCCAACGGATGACCATGTACAGATGGACCAAGCTGGAATGTGCGGAGACATTTTTGAGAGTGTTCATTCATCATATAATGTTGCTACAGGTAACATTATAAGCAACAGTTTAGTAGCAGAGACAGTAACTCATAGTTTGTTACCTCAGAATGAGCCTAAGACTTTAAATCAAGATATTGAGAAATCTGCACCAATTATAAATTTCAGTGCACAGAATAGTATGCTTCCTTCACAGAACATGA
Ensembl | human accession no.
NCBI accession no.
shipped in
ambient
storage temp.
−20°C
Quality Level
Gene Information
human ... ATMIN(23300), ATMIN(23300)
General description
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.
Legal Information
MISSION is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
10 - Combustible liquids
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
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Artem K Velichko et al.
Nucleic acids research, 47(13), 6811-6825 (2019-05-23)
The contribution of nucleoli to the cellular stress response has been discussed for over a decade. Stress-induced inhibition of RNA polymerase I-dependent transcription is hypothesized as a possible effector program in such a response. In this study, we report a
Caiyun G Li et al.
Cell reports, 26(5), 1333-1343 (2019-01-31)
Using proteomic approaches, we uncovered a DNA damage response (DDR) function for peroxisome proliferator activated receptor γ (PPARγ) through its interaction with the DNA damage sensor MRE11-RAD50-NBS1 (MRN) and the E3 ubiquitin ligase UBR5. We show that PPARγ promotes ATM
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