SHC002

Sigma-Aldrich

MISSION® pLKO.1-puro Non-Mammalian shRNA Control Plasmid DNA

Targets no known mammalian genes

Synonim(y):
MISSION® Control Vectors
Numer MDL:
NACRES:
NA.51

Poziom jakości

200

linia produktu

MISSION®

stężenie

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

wysyłka w ciągu

dry ice

temp. przechowywania

−20°C

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Zastosowanie

MISSION® pLKO.1-puro non-mammalian shRNA control plasmid DNA has been used:
  • to transduce RLE-6TN cells
  • for the validation of Oct4-green fluorescent protein (GFP) mouse embryonic fibroblasts (MEFs)
  • as a negative control for RNA knockdown

MISSION®pLKO.1-puro Non-Mammalian shRNA Control Plasmid DNA has been used:
  • for the knockdown of transmembrane prostate androgen-induced RNA (TMEPAI)
  • in the infection mixture for lentivirus preparation
  • for generating the puromycin-resistant ST14A (rat striatal neuronal cell line) cell populations
  • to induce Ago2 (argonaute-2) down-regulation

Informacje prawne

Use of this product is subject to one or more license agreements. For details, please see http://sigmaaldrich.com/missionlicense.
MISSION is a registered trademark of Sigma-Aldrich Co. LLC

storage_class_code

12 - Non Combustible Liquids

WGK Germany

WGK 1

Temperatura zapłonu °F

Not applicable

Temperatura zapłonu °C

Not applicable

Środki ochrony indywidualnej

Eyeshields, Gloves

Certyfikat analizy

Świadectwo pochodzenia

TMEPAI/PMEPA 1 enhances tumorigenic activities in lung cancer cells
Vo Nguyen TT, et al.
Cancer Science, 105(3), 334-341 (2014)
SFPQ?NONO and XLF function separately and together to promote DNA double-strand break repair via canonical nonhomologous end joining.
Jaafar l
Nucleic Acids Research, 45(4), 1848-1859 (2017)
Platelet-independent adhesion of calcium-loaded erythrocytes to von Willebrand factor.
Smeets MW
PLoS ONE, 12.3 (2017)
JNK1 Deficient Insulin-Producing Cells Are Protected against Interleukin-1?-Induced Apoptosis Associated with Abrogated Myc Expression.
Prause M
Journal of Diabetes Research (2016)
TRIM28 is an Epigenetic Barrier to Induced Pluripotent Stem Cell Reprogramming.
Miles DC
Stem Cells (2017)

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