LightShift™ Chemiluminescent EMSA Kit
LightShift™ Chemiluminescent EMSA Kit
Thermo Scientific™

LightShift™ Chemiluminescent EMSA Kit

Thermo Scientific LightShift Chemiluminescent EMSA Kit는 EMSA(electrophoretic mobility shift assay)를 실행하여 단백질-DNA 결합 상호작용을 확인하고 특성을 분석하는 매우 견고하고 민감도자세히 알아보기
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카탈로그 번호 20148
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100 reactions
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대량 주문 또는 맞춤형 요청
제품 가격(KRW)
937,000
Online offer
Ends: 31-Dec-2025
1,041,000
할인액 104,000 (10%)
100 reactions
카트에 추가하기
Thermo Scientific LightShift Chemiluminescent EMSA Kit는 EMSA(electrophoretic mobility shift assay)를 실행하여 단백질-DNA 결합 상호작용을 확인하고 특성을 분석하는 매우 견고하고 민감도 높은 시스템입니다. 이 키트에는 DNA 결합 상호작용을 설정하고 맞춤화하는 시약, 키트 시스템을 검사할 수 있는 DNA와 단백질 추출물로 구성된 대조군 세트, 비오틴이 표지된 DNA 표적을 프루빙(probing)할 수 있는 안정화된 streptavidin-HRP 접합체, 검출을 위한 매우 민감한 화학발광 기질 모듈이 들어 있습니다.

LightShift Chemiluminescent EMSA Kit의 특징:

• 핵 추출물에서 미량 단백질을 검출하는 우수한 성능
• 방사성 방식과 다이곡시제닌(digoxigenin) 방식보다 우수한 민감도
• 유명한 DNA-단백질 상호작용에 대해 이전에 수립한 결합 조건 적용 가능
• 신규 사용자가 우수한 분석법을 개발하고 결합 상호작용 특이성을 확인하는 데 사용되는 방법을 이해하는 데 유용한 EBNA 제어 시스템 포함

LightShift EMSA 검출 원리는 웨스턴 블롯(Western Blot)과 비슷합니다. 비오틴 말단 표지 duplex DNA는 핵 추출물이나 정제 인자를 사용해 배양되고 네이티브 겔에서 전기영동시킵니다. 그리고 나면 DNA는 신속하게(30분) 양의 나일론 막으로 전달되고, UV 교차연결되고, streptavidin-HRP 접합체로 조사되고 나서 기질을 사용해 배양됩니다. 표지부터 결과에 이르는 프로토콜을 단 하루만에 실시할 수 있습니다.

DNA와 단백질의 상호작용은 DNA 복제, 재조합 및 수복, 전사, 바이러스 어셈블리를 포함한 많은 세포 과정을 통제하는 데 있어 핵심적인 부분입니다. 유전자 조절 연구와 단백질:DNA 상호작용 확인에 핵심적인 한 가지 기법은 EMSA(electrophoretic mobility shift assay)입니다.

EMSA 기법은 비변성 polyacrylamide 또는 agarose 겔 전기영동을 적용하면 단백질:DNA 복합체가 자유 DNA 분자보다 느리게 이동한다는 관찰을 토대로 합니다. 단백질 결합 시 DNA 이동 속도는 바뀌거나 느려지기 때문에 이 분석을 겔 전이 또는 겔 지연 분석이라고도 합니다. EMSA의 개념이 정립되기 전에는 단백질:DNA 상호작용은 주로 nitrocellulose 필터-결합 분석을 사용해 연구되었습니다.

이 분석을 실시하려면 비오틴으로 말단 표지된 정제 DNA 표적, 검사할 단백질 추출물, 나일론 막(membrane), 기본 전기영동 장비만 있으면 됩니다. DNA 표적은 5' 또는 3' 비오틴 표지로 합성되거나 Thermo Scientific Biotin 3' End DNA Labeling Kit(제품 번호 89818)를 사용해 합성한 후 표지될 수 있습니다. 핵, 세포질, 전체 세포 단백질 추출물은 Thermo Scientific NE-PER Nuclear and Cytoplasmic Extraction Reagent Kit(제품 번호 78833)를 비롯한 다양한 방법으로 채취할 수 있습니다.

관련 자료:

단백질-핵산 상호작용 기술 가이드
단백질-DNA 상호작용 검출 기술 가이드
겔 전이 분석(EMSA) 기술 가이드

관련 제품:
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

추가 제품 데이터
Pierce G2 Fast Blotter를 사용한 Transfer EMSA 겔
For Research Use Only. Not for use in diagnostic procedures.
사양
어세이EMSA Assay
반응 수100
제품라인LightShift™
제품 유형Protein-DNA binding Interaction Assay Kit
수량100 Reactions
타겟 특이도Not Target-Specific
기술Enhanced Chemiluminescence, Membrane Blot, Gel Shift
검출 방법Chemiluminescent
형식Kit
Unit Size100 reactions

자주 묻는 질문(FAQ)

If the LightShift Chemiluminescent EMSA kit has been improperly stored (i.e., at room temperature, -20°C or +4°C), will it still work correctly?

The LightShift Chemiluminescent EMSA Kit is composed of two sets of components that require different storage temperatures. One component set consists of the chemiluminescent substrates and various buffers that are stored at 4°C. The other component set consists of the control DNAs and various optimization reagents that are stored at -20°C. The EBNA extract must be maintained at -20°C or it will lose activity (proteins will degrade). Short-term storage (overnight) of the other kit components at temperatures ranging from room temperature to -20°C will not adversely affect kit performance.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

I am using the LightShift Chemiluminescent EMSA kit. Can I probe for the proteins by performing a Western blot?

This has not been tested but may be possible. A better alternative is to perform a DNA binding protein pull-down assay using a probe. The following journal article is a good example of how the LightShift Chemiluminescent EMSA Kit and pull-down assays were used to detect a transcription factor bound to a DNA probe: Ragione, A.L., et al. (2003), J. Biol. Chem. 278(26):23360-8.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

I am using the LightShift Chemiluminescent EMSA kit. How much protein do I need for each reaction?

The amount of protein extract needed for a binding reaction depends on how much active DNA binding protein is in the sample. The LightShift Kit is sensitive and will easily detect 5 fmol of active protein bound to 5 fmol of biotinylated probe. If the protein being studied is abundant, 0.25 µg of a cell lysate may be sufficient for each binding reaction. However, if the protein of interest is rare, 10 µg or more of cell lysate may be needed. Using a large excess of protein extract may lead to high background signal and non-specific bands.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

What is a "supershift"?

A supershift assay is a method for positively identifying a protein:DNA interaction on an EMSA. An antibody (typically 1 µg) is added to the binding reaction. During electrophoresis, the antibody:protein:DNA complex migrates slowly, causing a “supershift” compared to the “shift” caused by a protein:DNA complex. Not all antibodies will cause a supershift. Some antibodies do not bind to proteins once they are bound to DNA. Some antibodies can prevent protein:DNA interactions but can still be used to confirm the identity of a protein that causes a shift in the absence of the antibody.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

Can the LightShift Chemiluminescent EMSA Kit be used to perform supershifts?

Yes, the LightShift Chemiluminescent EMSA Kit can be used to detect supershifts. However, not all antibodies will work for supershift assays. Some antibodies will prevent protein:DNA interactions. In addition, the order in which the components of the binding reaction are assembled may affect the results of a supershift assay. Generally, 1 µg antibody is added as the last component in the binding reaction. For examples of how the LightShift Chemiluminescent EMSA Kit was used to detect supershifts, see the following:

Adimoolam, S. and Ford, J.M. (2002). PNAS. 99(20):12985-90
Magid, R., et al. (2003). J. Biol. Chem. 278(35):32994-9
Ragione, F.D., et al. (2003). J. Biol. Chem. 278(26):23360-8
Rinaldi, A.L., et al. (2002). Cancer Research. 62(19):5451-6


Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

인용 및 참조 문헌 (26)

인용 및 참조 문헌
Abstract
Salidroside inhibits migration, invasion and angiogenesis of MDA‑MB 231 TNBC cells by regulating EGFR/Jak2/STAT3 signaling via MMP2.
Authors:Kang DY,Sp N,Kim DH,Joung YH,Lee HG,Park YM,Yang YM
Journal:International journal of oncology
PubMed ID:29901185
The major hallmarks of tumor progression are angiogenesis, migration and metastasis. Among the components of Rhodiola rosea, salidroside (p‑hydroxyphenethyl-β‑d-glucoside) is one of the most potent, and is present in all Rhodiola species. Recent data have revealed the anticancer effects of salidroside; however, the mechanism underlying its ability to inhibit tumor ... More
Exo70 is transcriptionally up-regulated by hepatic nuclear factor 4α and contributes to cell cycle control in hepatoma cells
Authors:Zhao Y, Hou J, Mi P, Mao L, Xu L, Zhang Y, Xiao L, Cao H, Zhang W, Zhang B, Song G, Hu T, Zhan YY.
Journal:Oncotarget
PubMed ID:26848864
Exo70, a member of the exocyst complex, is involved in cell exocytosis, migration, invasion and autophagy. However, the expression regulation and function of Exo70 in hepatocellular carcinoma are still poorly understood. In this study, we found Exo70 expression in human hepatoma cells was greatly reduced after knocking down hepatic nuclear ... More
Disruption of chaperone-mediated autophagy-dependent degradation of MEF2A by oxidative stress-induced lysosome destabilization.
Authors:Zhang L,Sun Y,Fei M,Tan C,Wu J,Zheng J,Tang J,Sun W,Lv Z,Bao J,Xu Q,Yu H
Journal:Autophagy
PubMed ID:24879151
Oxidative stress has been implicated in both normal aging and various neurodegenerative disorders and it may be a major cause of neuronal death. Chaperone-mediated autophagy (CMA) targets selective cytoplasmic proteins for degradation by lysosomes and protects neurons against various extracellular stimuli including oxidative stress. MEF2A (myocyte enhancer factor 2A), a ... More
Estrogen Regulates Angiotensin II Receptor Expression Patterns and Protects the Heart from Ischemic Injury in Female Rats.
Authors:Xue Q, Xiao D, Zhang L
Journal:
PubMed ID:25972014
'Previous studies have shown that female offspring are resistant to fetal stress-induced programming of ischemic-sensitive phenotype in the heart; however, the mechanisms responsible remain unclear. The present study tested the hypothesis that estrogen plays a role in protecting females in fetal programming of increased heart vulnerability. Pregnant rats were divided ... More
The solution structure of the forkhead box-O DNA binding domain of Brugia malayi DAF-16a.
Authors:Casper SK, Schoeller SJ, Zgoba DM, Phillips AJ, Morien TJ, Chaffee GR, Sackett PC, Peterson FC, Crossgrove K, Veldkamp CT
Journal:
PubMed ID:25297652
Brugia malayi is a parasitic nematode that causes lymphatic filariasis in humans. Here the solution structure of the forkhead DNA binding domain of Brugia malayi DAF-16a, a putative ortholog of Caenorhabditis elegans DAF-16, is reported. It is believed to be the first structure of a forkhead or winged helix domain ... More