UltraPure™ Agarose
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UltraPure™ Agarose
인용 및 참조 문헌 (20)
Invitrogen™

UltraPure™ Agarose

Green features
UltraPure™ Agarose는 agarose 겔 전기영동법에서 크기 기반 핵산 분리에 사용하는 polysaccharide (아래 구조 참조)입니다. UltraPure™ Agarose는 500 bp to >자세히 알아보기
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카탈로그 번호수량
16500500500 g
16500100100 g
카탈로그 번호 16500500
제품 가격(KRW)
911,000
線上優惠
Ends: 31-Dec-2025
1,012,000
할인액 101,000 (10%)
Each
카트에 추가하기
수량:
500 g
대량 주문 또는 맞춤형 요청
제품 가격(KRW)
911,000
線上優惠
Ends: 31-Dec-2025
1,012,000
할인액 101,000 (10%)
Each
카트에 추가하기
UltraPure™ Agarose는 agarose 겔 전기영동법에서 크기 기반 핵산 분리에 사용하는 polysaccharide (아래 구조 참조)입니다. UltraPure™ Agarose는 500 bp to > 20 kb DNA 및 RNA fragment 분해에 이상적입니다.

• 일상 어플리케이션에서 DNA 및 RNA 분석과 회수에 이상적
• 튼튼한 겔 구조로 취급이 편리하고 파손 위험이 적습니다.
• Ouchterlony (항원항체 상호작용 분석) 및 RID (radial immunodiffusion) (항원 정량법) 등 단백질 전기영동에 사용할 수 있습니다.

포장의 개선
친환경적인 새로운 포장으로 원래 병보다 플라스틱 사용량을 75% 줄였습니다. 즉, 제조 시 사용되는 에너지와 원료, 매립지 폐기물을 줄입니다. 또한 따르기 쉬운 입구로 흘릴 위험과 오염 가능성을 낮춥니다.

품질 검사 성능
UltraPure™ Agarose 성능은 성상, 수분 함량, 겔 강도, 겔화 온도, 융해 온도, 황함량, 전기삼투, DNase/RNase 분석 기준을 모두 만족합니다.

UltraPure™ Agarose (카탈로그 번호 16500-100)는 이전에 카탈로그 번호 15510-019로 판매되던 제품을 대체합니다.

본 제품은 연구용으로만 사용가능 합니다. 치료 또는 진단 목적으로 동물이나 인간에 사용할 수 없습니다.
For Research Use Only. Not for use in diagnostic procedures.
사양
용도(애플리케이션)Nucleic Acid Gel Electrophoresis, Protein Electrophoresis, Blotting
형태Powder
젤 호환성Agarose Gels
그린 기능Sustainable packaging
용융점Standard Melting Point
반응 수2500
제품라인UltraPure
제품 유형Agarose
수량500 g
배송 조건Room Temperature
분리 범위100 to >30000 bp
Unit SizeEach
구성 및 보관
Contents: 1 pouch containing 500 g of UltraPure™ Agarose
Storage: 15°C to 30°C

자주 묻는 질문(FAQ)

I want to pour my own gels. Which agarose should I use?

Our UltraPure Agarose is standard melting-point agarose designed for routine separation and analysis of DNA and RNA fragments in the 500-23,000 nt range. UltraPure Agarose 1000 is a specialized agarose that provides higher resolution of PCR fragments and other short DNA fragments. We also offer an UltraPure Low Melting Point Agarose, which is ideal for resolving DNA fragments from 10 to 1,000 bp with a low melting temperature of 65°C or less.

How can generation of replication competent adenoviruses be avoided when using your pSilencer adeno 1.0-CMV System?

Although there is only a very small chance of creating replication competent virus, steps should still be taken to avoid added risk. The virus is expanded in two rounds of amplification, and all secondary expansions should be performed from an initial expansion stock. Secondary amplifications in HEK293 cells should not be performed from the stock of another secondary expansion, as this could increase the chance of making replication competent virus. See the product manual for more detail and guidelines for screening.

Find additional tips, troubleshooting help, and resources within our RNAi Support Center.

인용 및 참조 문헌 (20)

인용 및 참조 문헌
Abstract
Proteomic analysis reveals presence of platelet microparticles in endothelial progenitor cell cultures.
Authors:Prokopi M, Pula G, Mayr U, Devue C, Gallagher J, Xiao Q, Boulanger CM, Westwood N, Urbich C, Willeit J, Steiner M, Breuss J, Xu Q, Kiechl S, Mayr M,
Journal:Blood
PubMed ID:19369228
'The concept of endothelial progenitor cells (EPCs) has attracted considerable interest in cardiovascular research, but despite a decade of research there are still no specific markers for EPCs and results from clinical trials remain controversial. Using liquid chromatography-tandem mass spectrometry, we analyzed the protein composition of microparticles (MPs) originating from ... More
A phantom for diffusion-weighted MRI (DW-MRI).
Authors:Lavdas I, Behan KC, Papadaki A, McRobbie DW, Aboagye EO,
Journal:J Magn Reson Imaging
PubMed ID:23576443
'PURPOSE: To develop tissue-equivalent diffusivity materials and build a spherical diffusion phantom which mimics the conditions typically found in biological tissues. Also, to assess the reproducibility of ADC measurements from a whole-body diffusion protocol. MATERIALS AND METHODS: Nickel-doped agarose/sucrose gels were manufactured and used to build a spherical diffusion phantom ... More
Determinants of nucleosome organization in primary human cells.
Authors:Valouev A, Johnson SM, Boyd SD, Smith CL, Fire AZ, Sidow A,
Journal:Nature
PubMed ID:21602827
'Nucleosomes are the basic packaging units of chromatin, modulating accessibility of regulatory proteins to DNA and thus influencing eukaryotic gene regulation. Elaborate chromatin remodelling mechanisms have evolved that govern nucleosome organization at promoters, regulatory elements, and other functional regions in the genome. Analyses of chromatin landscape have uncovered a variety ... More
Controlling cell position in complex heterotypic 3D microtissues by tissue fusion.
Authors:Rago AP, Dean DM, Morgan JR,
Journal:Biotechnol Bioeng
PubMed ID:19012266
'Tissue fusion and cell sorting are processes fundamental to developmental biology with applications in tissue engineering. We have designed a fusion assay to investigate the factors governing the fusion of microtissues and the cell sorting that occurs after fusion. Normal human fibroblast (NHF) spheroids were self-assembled and cultured for 1, ... More
Host alternation of chikungunya virus increases fitness while restricting population diversity and adaptability to novel selective pressures.
Authors:Coffey LL, Vignuzzi M,
Journal:J Virol
PubMed ID:21047966
'The mechanisms by which RNA arboviruses, including chikungunya virus (CHIKV), evolve and maintain the ability to infect vertebrate and invertebrate hosts are poorly understood. To understand how host specificity shapes arbovirus populations, we studied CHIKV populations passaged alternately between invertebrate and vertebrate cells (invertebrate ? vertebrate) to simulate natural alternation ... More
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