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20148-- LightShift Chemiluminescent EMSA Kit

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  • 公司名稱 北京華夏遠(yuǎn)洋科技有限公司
  • 品牌 Thermofisher Scientific/賽默飛世爾
  • 型號 20148--
  • 產(chǎn)地 Thermo pierce
  • 廠商性質(zhì) 代理商
  • 更新時間 2017/8/13 23:13:12
  • 訪問次數(shù) 1814
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LightShift Chemiluminescent EMSA Kit

 

The Thermo Scientific LightShift Chemiluminescent EMSA Kit is an extraordinarily robust and sensitive system for performing electrophoretic mobility shift assays (EMSA) to identify and characterize protein-DNA binding interactions.
The kit includes reagents for setting up and customizing DNA binding reactions, a control set of DNA and protein extract to test the kit system, stabilized streptavidin-HRP conjugate to probe for the biotinlabeled DNA target, and an exceptionally sensitive chemiluminescent substrate module for detection.
Highlights:
  • Excellent for detecting low-abundance proteins in nuclear extracts
  • Sensitivity that surpasses radioactive and digoxigenin methods
  • Compatible with previously established binding conditions for popular DNA-protein interactions
  • Includes EBNA control system to help new users develop a working assay and understand the methods used to confirm binding interaction specificity
Product Details:
The principle for LightShift EMSA Detection is similar to a Western blot. Biotin end-labeled duplex DNA is incubated with a nuclear extract or purified factor and electrophoresed on a native gel. The DNA is then rapidly (30 minutes) transferred to a positive nylon membrane, UV crosslinked, probed with streptavidin-HRP conjugate and incubated with the substrate. The protocol from labeling to results can be accomplished in a single day.

Summary of chemiluminescent nonradioactive EMSA protocol for gel shift assays
Procedure summary for the Thermo Scientific LightShift EMSA Kit.

The interaction of proteins with DNA is central to the control of many cellular processes including DNA replication, recombination and repair, transcription, and viral assembly. One technique that is central to studying gene regulation and determining protein:DNA interactions is the electrophoretic mobility shift assay (EMSA).
The EMSA technique is based on the observation that protein:DNA complexes migrate more slowly than free DNA molecules when subjected to non-denaturing polyacrylamide or agarose gel electrophoresis. Because the rate of DNA migration is shifted or retarded upon protein binding, the assay is also referred to as a gel shift or gel retardation assay. Until conception of the EMSA protein:DNA interactions were studied primarily by nitrocellulose filter-binding assays.
All that is needed to perform the assay is purified DNA target that has been end-labeled with biotin, the protein extract to be tested, nylon membrane and basic electrophoresis equipment. DNA targets can be synthesized with 5' or 3' biotin labels or they can be labeled after synthesis using the Thermo Scientific Biotin 3' End DNA Labeling Kit (Product No. 89818). Nuclear, cytosolic or whole cell protein extracts can be obtained by a variety of methods, including the Thermo Scientific NE-PER Nuclear and Cytoplasmic Extraction Reagent Kit (Product No. 78833).

EMSA results using the EBNA control system. Biotin-labeled 60 bp duplex bearing the EBNA-1 binding sequence was incubated with an extract in which the EBNA-1 protein was overexpressed. The binding buffer was supplemented with 50 ng/µl poly(dI•dC), 10% glycerol and 0.05% NP-40. Exposure time was 30 seconds with X-ray film.
Control system for EMSA detection method validation
 
Example application data for chemiluminescent EMSA and gel shift assays.
Chemiluminescent EMSA of four different DNA:protein complexes. Biotin-labeled target duplexes ranged in size from 21-25 bp. The EBNA reactions were supplemented with 2.5% glycerol and 0.05% NP-40, and the AP1 reactions were supplemented with 10% glycerol. The source of the Oct-1, AP1 and NF-kB transcription factors was a HeLa nuclear extract. EBNA-1 extract is provided as a control in the kit. Unlabeled specific competitor sequences (where used) were present at a 200-fold molar excess over labeled target. X-ray film exposure times for each system ranged from 2 minutes for EBNA, Oct-1 and AP1, and 5 minutes for NF-kB.
 
 sensitivity
 
More sensitive EMSA detection than other gel shift assay methods. Comparison of the LightShift EMSA Kit to a popular digoxigenin-based EMSA kit and a radioactive method. Serial dilutions of a labeled DNA duplex were electrophoresed on a 6% polyacrylamide gel and detected according to the manufacturer’s instructions. Comparable sensitivity (<50 attomoles) was achieved with the LightShift EMSA Kit and radioactivity (2,000 cpm 32-P/fmol), although a significantly longer exposure was required for the 32P-labeled DNA. Equivalent exposures using the two chemiluminescent kits showed that the sensitivity of the LightShift EMSA Kit was approximay eight-fold greater than that of the digoxigenin kit.
 
Better EMSA results in less time. Comparison of the LightShift EMSA Kit to a popular digoxigenin-based EMSA kit and a radioactive method. A 22-bp duplex containing the binding sequence for the transcription factor Oct-1 was labeled for use in either the LightShift EMSA Kit, a digoxigenin-based EMSA kit or with 32P using T4 polynucleotide kinase (40,000 cpm/reaction) for use in traditional radioactive EMSA. Binding reactions were equivalent in that 20 fmol duplex was incubated with 6.8 µg HeLa cell NE-PER Nuclear Extract (where indicated). The chemiluminescent kits were used according to the manufacturer’s instructions. For the radioactive EMSA, the gel was exposed directly to X-ray film using screens.
Performance of the  vs. radioactive (32P) EMSA

References:
  1. Guadix J. A. et al. (2011) Wt1 controls retinoic acid signalling in embryonic epicardium through transcriptional activation of Raldh2. Development. 138, 1093-7.
  2. Gau B.-H. et al. (2011) FUBP3 interacts with FGF9 3' microsalite and positively regulates FGF9 translation. Nucleic Acids Res., gkq1295.
  3. Cai Q. et al. (2011) Replication and functional genomic analyses of the breast cancer susceptibility locus at 6q25.1 Generalize its importance in women of Chinese, Japanese, and European ancestry. Cancer Res. 71, 1344-55.
  4. Yoo C. Y. et al. (2010) The Arabidopsis GTL1 transcription factor regulates water use efficiency and drought tolerance by modulating stomatal density via transrepression of SDD1. Plant Cell. 22, 4128-41.
  5. Sultana H. et al. (2010) Anaplasma phagocytophilum induces actin phosphorylation to selectively regulate gene transcription in Ixodes scapularis ticks. J. Exp. Med. 207, 1727-43.
  6. Husain M. et al. (2010) Redox sensor SsrB Cys203 enhances Salmonella fitness against nitric oxide generated in the host immune response to oral infection. PNAS. 107, 14396-401.

Related Resources:
Tech Tip: Modify and label oligonucleotide 5´ phosphate groups
Tech Tip: Anneal complementary pairs of oligonucleotides
LightShift Chemiluminescent EMSA FAQ
Related Products:
Biotin 3´ End DNA Labeling Kit
NE-PER Nuclear and Cytoplasmic Protein Extraction Reagent Kit
Biodyne B Nylon Membrane for Chemiluminescent EMSA
Chemiluminescent Nucleic Acid Detection Module
LightShift Chemiluminescent RNA EMSA Kit
Pierce Protocols App
Ordering Information
 
 
Product # Description Pkg. Size Instructions MSDS CofA Price
20148
Sufficient components for 100 binding reactions and detection reagents for ~800 cm2 of membrane.

Kit Contents:

LightShift EMSA Optimization and Control Kit (20148X, available separay)
10X Binding Buffer, 1mL
Biotin-EBNA Control DNA, 50µL
Unlabeled EBNA DNA, 50µL
EBNA Extract, 125µL
Poly (dI•dC), 125µL
50% Glycerol, 500µL
1% NP-40, 500µL
1 M KCl, 1mL
100 mM MgCl2, 500µL
200 mM EDTA pH 8.0, 500µL
5X Loading Buffer, 1mL

Chemiluminescent Nucleic Acid Detection Module (89880, available separay)
Stabilized Streptavidin-Horseradish Peroxidase Conjugate, 1.5mL
Luminol/Enhancer Solution, 80mL
Stable Peroxide Solution, 80mL
Blocking Buffer, 500mL
4X Wash Buffer, 500mL
Substrate Equilibration Buffer, 500mL
Kit Product Instructions for product #20148 MSDS for product #20148 Certificate of Analysis for product #20148

Local contact
20148X LightShift EMSA Optimization and Control Kit
Kit Contents:
10X Binding Buffer, 1mL
Biotin-EBNA Control DNA, 50µL
Unlabeled EBNA DNA, 50µL
EBNA Extract, 125µL
Poly (dI•dC), 125µL
50% Glycerol, 500µL
1% NP-40, 500µL
1 M KCl, 1mL
100 mM MgCl2, 500µL
200 mM EDTA pH 8.0, 500µL
5X Loading Buffer, 1mL
Kit Product Instructions for product #20148X LightShift EMSA Optimization and Control Kit MSDS for product #20148X LightShift EMSA Optimization and Control Kit Certificate of Analysis for product #20148X LightShift EMSA Optimization and Control Kit

Local contact
20148E LightShift Poly (dI-dC)
1µg/µL solution
125 µL MSDS for product #20148E LightShift Poly (dI-dC)

Local contact



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