Dynabeads™ MyOne™ Streptavidin T1
Dynabeads™ MyOne™ Streptavidin T1
Invitrogen™

Dynabeads™ MyOne™ Streptavidin T1

Dynabeads MyOne Streptavidin T1은 바이오티닐화 핵산, 항체 또는 기타 바이오티닐화 리간드 및 타겟의 분리와 취급에 사용되는 gold standard입니다. streptavidin-biotin 상호작용의자세히 알아보기
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카탈로그 번호제품 유형수량
11205DDynabeads™ M-280 Streptavidin2 mL
65001Dynabeads™ MyOne™ Streptavidin C12 mL
65002Dynabeads™ MyOne™ Streptavidin C110 mL
65604DDynabeads™ MyOne™ Streptavidin T150 mL
65602Dynabeads™ MyOne™ Streptavidin T110 mL
65601Dynabeads™ MyOne™ Streptavidin T12 mL
65605DDynabeads™ Streptavidin for Target Enrichment2 mL
65606DDynabeads™ Streptavidin for Target Enrichment10 mL
65607DDynabeads™ Streptavidin for Target Enrichment50 mL
11206DDynabeads™ M-280 Streptavidin10 mL
60210Dynabeads™ M-280 Streptavidin100 mL
65305Dynabeads™ M-270 Streptavidin2 mL
65306Dynabeads™ M-270 Streptavidin10 mL
60101Dynabeads™ kilobaseBINDER™ Kit200 Isolations
65801DDynabeads™ Streptavidin Trial Kit4 x 1 mL
카탈로그 번호 11205D
제품 가격(KRW)
785,000
Online offer
Ends: 31-Dec-2025
872,000
할인액 87,000 (10%)
Each
카트에 추가하기
제품 유형:
Dynabeads™ M-280 Streptavidin
수량:
2 mL
제품 가격(KRW)
785,000
Online offer
Ends: 31-Dec-2025
872,000
할인액 87,000 (10%)
Each
카트에 추가하기

Dynabeads MyOne Streptavidin T1은 바이오티닐화 핵산, 항체 또는 기타 바이오티닐화 리간드 및 타겟의 분리와 취급에 사용되는 gold standard입니다. streptavidin-biotin 상호작용의 매우 높은 결합 친화도(Kd=10-15)는 수 많은 응용 분야에 사용됩니다. 장점 및 특징:

• 모든 바이오티닐화 분자의 직접 및 빠른 분리
• 부드럽고 효율적인 액상 반응 kinetics로 유연한 프로토콜
• 단백질, 펩타이드, 항체의 결합에 최적화된 low-charged 및 neutral 비드
• 크기가 작지만 균일하여 mg 비드당 표면적이 크고, 따라서 표적 분자에 대한 용량이 높음
• 낮은 침강 속도와 높은 철 함량을 바탕으로 빠른 마그네틱 분리가 가능함
• 바이오마그네틱(biomagnetic) 프로토콜은 자동화 플랫폼에 쉽게 적용 가능
• 높은 배치 간(batch-to-batch) 재현성으로 응용 분야에서 일관된 결과 보장

Dynabeads MyOne Streptavidin T1 정보
이 독특한 초상자성 비드는 지름이 1 µm이며, 다중 층이 아닌 단층의 재조합 스트렙타비딘(streptavidin)이 표면에 공유 결합되어 있으며 BSA로 블락되어 있습니다. 이 단층의 스트렙타비딘은 자유 비오틴 뿐만 아니라 바이오티닐화 리간드/타겟의 결합에도 이용가능한 입체적인 비오틴 결합 부위가 많이 있습니다. 이 비드는 빠른 액상 반응 속도를 보여줍니다. 이 비드의 특이적으로 정의된 표면은 효율적인 캡쳐, 분리, 다운스트림 핸들링( downstream handling)을 가능하게 합니다. 단층의 스트렙타비딘은 누출이 거의 없고 과도하게 흡수되는 스트렙타비딘이 없어 배치(batch) 일관성과 결과의 재현성을 보장합니다. 1 µm Dynabeads MyOne은 넓은 표면적, 고용량, 효율적인 마그네틱 끌어당김(magnetic pull), 인큐베이션 중 느린 침강 속도 등의 특징이 있습니다. 고처리량(High throughput)이 중요한 경우에는 자동화된 프로토콜을 사용하여 맞춤화가 가능합니다.

응용 분야
지난 15년 동안 streptavidin-coupled Dynabeads는 매우 다양한 응용 분야에 사용되어 왔습니다. 주요 응용 분야로는 단일 가닥 DNA 템플릿 준비, RNA 및 DNA 결합 단백질 분리, 큰 DNA fragment 고정, 시퀀싱(sequencing) 산물 정제, 특이적 핵산 캡쳐 등이 있습니다. 이 비드는 자동 프로세스에 쉽게 적용됩니다. Dynabeads는 전 세계에서 25,000개 이상의 일상적인 IVD 기기에 사용되고 있습니다.

결합 용량
분자의 크기와 바이오티닐화 절차는 결합 능력에 영향을 미칩니다. 이 결합 용량은 입체적 가용성(steric availability), 비드와 분자간 및 분자들 간의 전하 상호작용에 따라 달라집니다. 고정화 후 비드 표면 상에서 이용가능한 비오틴 결합 부위는 스트렙타비딘 분자당 2개 또는 3개입니다. 1 mg의 Dynabeads MyOne Streptavidin T1은 일반적으로 다음과 결합합니다.

• 950–1500 pmoles 자유 비오틴
• ∼20µg 바이오티닐화 IgG
• ∼400 pmol 바이오티닐화 펩타이드
• ∼20µg ds-DNA
• ∼400 pmol ss-올리고뉴클레오티드

연구용으로만 사용하십시오. 진단용으로는 사용할 수 없습니다.
사양
비드 유형Magnetic polystyrene-based beads covalently coupled with recombinant Streptavidin
결합 특성490-750 pmol free biotin/mg beads
인증/적합성ISO9001 and ISO13485
농도10 mg/mL
직경(미터법)2.8 μm (CV < 5%)
용도(애플리케이션)Immunoassays, biopanning, etc, requiring high specificity, low background binding, and ease of handling
용도(장비)KingFisher™ Sample Purification System, DynaMag™ magnets
고처리량 호환성High-throughput Compatible
제품라인Dynabeads
제품 유형Dynabeads™ M-280 Streptavidin
수량2 mL
규제 상태For Research Use Only
유통 기한36 months from date of manufacture
배송 조건Ambient Temperature
표면 기능성Tosylactivated hydrophobic surface blocked with BSA
형식Beads in Suspension
Isolation TechnologyMagnetic Bead
Unit SizeEach
구성 및 보관
Dynabeads M-280 Streptavidin is supplied in PBS, pH 7.4 with 0.02% NaN3. Store at 2°C to 8°C.

자주 묻는 질문(FAQ)

Can Dynabeads Streptavidin magnetic beads be boiled?

We do not recommend this as streptavidin becomes hydrophobic and aggregates during denaturation.

I am getting high background using Dynabeads M-280 Streptavidin magnetic beads. How can I prevent this from happening?

The background might be caused by nonspecific binding to the BSA on the bead surface. Alternatively, high background might be caused by nonspecific binding to streptavidin. Increasing either the pH or the salt concentration might help reduce the binding. Dynabeads M-270 Streptavidin magnetic beads might be a better alternative; these beads are not coated with BSA and are hydrophilic, as they are based upon carboxylic acid chemistry.

My Dynabeads magnetic beads are not pelleting well with the magnet. Do you have any suggestions for me?

Please review the following possibilities for why your Dynabeads magnetic beads are not pelleting:

- The solution is too viscous.
- The beads have formed aggregates because of protein-protein interaction.

Try these suggestions: - Increase separation time (leave tub on magnet for 2-5 minutes)
- Add DNase I to the lysate (~0.01 mg/mL)
- Increase the Tween 20 concentration to ~0.05% of the binding and/or washing buffer.
- Add up to 20 mM beta-merecaptoethanol to the binding and/or wash buffers.

Find additional tips, troubleshooting help, and resources within our Dynabeads Nucleic Acid Purification Support Center.

My Dynabeads M-280 Streptavidin magnetic beads were accidentally frozen. Can I still use them?

Yes, you can still use them. To test stability at low temperature in-house, the Dynabeads M-280 Streptavidin beads were placed at -20 degrees C for 24 hrs and then transferred to room temperature (15-25 degrees C) for 72 hrs. This freeze/thaw cycle was repeated 4 times and the beads were stored at 2-8 degrees C for 60 months. The biotin binding capacity was then tested and was seen to be within our specifications.

Find additional tips, troubleshooting help, and resources within our Dynabeads Nucleic Acid Purification Support Center.

Which streptavidin-conjugated Dynabeads magnetic beads are the right beads for my application?

Which product to choose depends on the properties of your sample, the buffers and solutions applied, as well as the downstream application. In general, all Dynabeads Streptavidin beads can be used in applications involving biotinylated ligands; however, some beads may perform better than others in particular applications due to their characteristics. Dynabeads M-280 Streptavidin beads and Dynabeads MyOne Streptavidin T1 beads are commonly used for protein and nucleic acid applications. Dynabeads M-270 Streptavidin beads and MyOne Streptavidin C1 beads are preferred for nucleic acid diagnostics, specifically with samples that have a high concentration of chaotropic salts, immunoassays involving small biotinylated antigens, and in applications that are not compatible with BSA, as these beads are not blocked with BSA. Dynabeads MyOne Streptavidin beads offer increased binding capacity and slower sedimentation rate, making them ideal for automated applications and when larger amounts of a biotinylated compound or its specific target need to be isolated. Please see the selection guide here ( https://www.thermofisher.com/us/en/home/brands/product-brand/dynal/streptavidin-coupled-dynabeads.html?icid=fr-strep-1).

인용 및 참조 문헌 (16)

인용 및 참조 문헌
Abstract
Detection of tyrosinase mRNA in melanoma by reverse transcription-PCR and electrochemiluminescence.
Authors:O&apos;Connell CD, Juhasz A, Kuo C, Reeder DJ, Hoon DS,
Journal:Clin Chem
PubMed ID:9625038
Increased sensitivity and improved quantitation of analytical tests used in biotechnology and clinical chemistry are goals of many laboratories. We have used tyrosinase primers to specifically amplify by RT-PCR the tyrosinase mRNA expressed by the M12 melanoma cell line in a background of mRNA from breast cancer cells. An electrochemiluminescence ... More
AID-induced decrease in topoisomerase 1 induces DNA structural alteration and DNA cleavage for class switch recombination.
Authors:Kobayashi M, Aida M, Nagaoka H, Begum NA, Kitawaki Y, Nakata M, Stanlie A, Doi T, Kato L, Okazaki IM, Shinkura R, Muramatsu M, Kinoshita K, Honjo T,
Journal:Proc Natl Acad Sci U S A
PubMed ID:20018730
'To initiate class switch recombination (CSR) activation-induced cytidine deaminase (AID) induces staggered nick cleavage in the S region, which lies 5'' to each Ig constant region gene and is rich in palindromic sequences. Topoisomerase 1 (Top1) controls the supercoiling of DNA by nicking, rotating, and religating one strand of DNA. ... More
Recommended mass spectrometry-based strategies to identify botulinum neurotoxin-containing samples.
Authors:Kalb SR, Baudys J, Wang D, Barr JR
Journal:
PubMed ID:25996606
'Botulinum neurotoxins (BoNTs) cause the disease called botulism, which can be lethal. BoNTs are proteins secreted by some species of clostridia and are known to cause paralysis by interfering with nerve impulse transmission. Although the human lethal dose of BoNT is not accurately known, it is estimated to be between ... More
Using phage and yeast display to select hundreds of monoclonal antibodies: application to antigen 85, a tuberculosis biomarker.
Authors:Ferrara F, Naranjo LA, Kumar S, Gaiotto T, Mukundan H, Swanson B, Bradbury AR
Journal:PLoS One
PubMed ID:23166701
'Current diagnostic methods for tuberculosis (TB), a major global health challenge that kills nearly two million people annually, are time-consuming and inadequate. During infection a number of bacterial molecules that play a role in the infective process are released and have been proposed as biomarkers for early TB diagnosis. Antigen ... More
PCR-free detection of genetically modified organisms using magnetic capture technology and fluorescence cross-correlation spectroscopy.
Authors:Zhou X, Xing D, Tang Y, Chen WR,
Journal:PLoS One
PubMed ID:19956680
'The safety of genetically modified organisms (GMOs) has attracted much attention recently. Polymerase chain reaction (PCR) amplification is a common method used in the identification of GMOs. However, a major disadvantage of PCR is the potential amplification of non-target DNA, causing false-positive identification. Thus, there remains a need for a ... More