New England Biolabs
To access your account, log in or register.
Products Technical Reference Customer Service My NEB Account
Contact NEB About Us Site Map Request a Catalog OEM at NEB International Orders Freezer Program Quick Order
Related Information
Protocols for Estrogen Receptor α ShortCut® siRNA Mix
FAQs for RNAi and RNA Enzymes
Technical Reference for RNAi and RNA Enzymes
Favorite Tools
Enzyme Finder
NEBcutter
NEBuffer Chart
Double Digest Finder
Isoschizomers
DNA Sequences
and Maps
REBASE
Related Products
Companion Products
Estrogen Receptor β ShortCut® siRNA Mix
Fluorescein-siRNA Transfection Control
Lit28i Polylinker ShortCut® siRNA Mix
TransPass™ R1 Transfection Reagent
TransPass™ R2 Transfection Reagent
Estrogen Receptor α ShortCut® siRNA Mix
Catalog # Size Concentration Price Qty  
N2010S 1 nmol 10 μM $195.00
Prices are in US dollars and valid only for US orders.
Download:MSDS PDF


Description:
A heterogeneous mixture of 21-23 bp short interfering RNAs (siRNA) that induces effective silencing (RNAi) of Estrogen Receptor a in mammalian cell lines.

Estrogen Receptor α is an estrogen-activated transcription factor involved in maintenance and regulation of reproductive tissues and the central nervous system (1,2).

Recommended Usage Concentration: 5 to 20 nM





Figure 1: 15 ng (1 pmol) of ShortCut siRNA mix is run along with synthetic 17, 21 and 25 bp siRNA markers (NEB #N2101) on a 20% TBE polyacrylamide gel electrophoresis.





Figure 2: U2OS cells stably transfected with an inducible estrogen receptor α construct were transfected with different concentrations of Estrogen Receptor α ShortCut siRNA Mix (+) (3). Effective silencing of Estrogen Receptor α is achieved at low concentrations 24 hours post-transfection. Estrogen Receptor α was detected in a Western blot of cell lysates using Dako (M7047) anti-Estrogen Receptor α Antibody and actin loading control was detected using (Sigma A-2066) Antibody.



Background:
ShortCut® siRNA Mixes are highly potent, validated silencing mixtures generated by NEB's proprietary ShortCut RNase III technology. The section of mRNA sequence that each mixture targets has been selected to ensure no significant sequence identity to other genes. Each mixture is a unique combination of many individual siRNAs that work collectively to knock down the target gene. As a result, the mixtures can be used at extremely low concentration (typically 1-20 nM) which minimizes the potential for off-target effects.

Source:
A 537 bp DNA template derived from human Estrogen Receptor α cDNA (accession number NM_000125, coordinates 369-905) was used to generate dsRNA which was processed by ShortCut RNase III to produce the siRNA Mix.


Reaction & Storage Conditions


Concentration:
10 μM

Storage Conditions:
20 mM KCl
0.5 mM EDTA
10 mM Na-HEPES
pH 7.0 @ 25°C

Storage Temperature:
-20°C


Notes


General notes:
  1. It is important to maintain healthy cells. Some cell lines become more sensitive to transfection agents after a large number of passages. It is advisable to use cells subjected to a similar number of passages to ensure reproducible transfection results in different experiments.
  2. It is recommended that control transfections be performed by varying cell confluence and using different amounts of TransPass Transfection Reagent. In general, low cell density or too much transfection reagent increase the risk of cell toxicity. The medium may be replaced 24 hours after transfection with fresh complete medium to increase cell viability.
    In order to easily estimate the efficiency of transfection of particular cell lines use the Fluorescein-siRNA Transfection Control (NEB #N2100S).
  3. TransPass R1 Transfection Reagent has been used to successfully transfect siRNAs in many cell lines including: A549, C6, CHO, COS-7, HEK293, NIH 3T3, HepG2, HCT116, HeLa, Jurkat, MCF-7, U2OS, 3T3-L1 preadipocytes.
  4. Transfection of siRNA Mixtures: The transfection of siRNA must be optimal in order to obtain maximum silencing of a target gene. Optimizing the following parameters may be necessary in order to maximize the transfection efficiency for a particular cell line: the cell density at the time of transfection, the amount of transfection reagent, the amount of siRNA and the culture incubation time before analysis.

Quality Control for Current Lot


Quality control values for a specific lot can be found on the datacard which accompanies each product.

Quality Assurance Statement:
Purified by ion exchange chromatography free of contaminating large molecular weight dsRNA, ssRNA, DNA, bacteria and protein.


References


  1. Mangelsdorf, D.J. et.al. (1995) Cell, 83, 835-839.
  2. Glass, C.K. and Rosenfeld, M.G. (2000) Genes Dev., 14, 121-141.
  3. Tzagarakis-Foster, C., (UCSF), unpublished observations.


Companion Products


Estrogen Receptor β ShortCut® siRNA Mix
Fluorescein-siRNA Transfection Control
Lit28i Polylinker ShortCut® siRNA Mix
TransPass™ R1 Transfection Reagent
TransPass™ R2 Transfection Reagent


Legal


Licenses/Patents/Disclaimers:
Notice to Buyer/User: Commercial use of ShortCut® siRNA Mixes may require a license from New England Biolabs, Inc. Use of ShortCut® siRNA Mixes for RNA interference may require a license from the Carnegie Institution of Washington. For further information, contact the Director of Administration and Finance at the Carnegie Institute of Washington at 1530 P Street N.W., Washington, DC 20005-1910. Tel: 202-939-1118.

Privacy, Limitations, Warranty, Disclaimer, Copyright & Trademark