Dynabeads™ Sheep anti-Rabbit IgG는 면역글로불린 또는 다른 표적 분자를 간단하고 효율적으로 결합하게 도와주는 고형 보조제입니다. 균일하게 배치된 beads는 지름이 2.82.8자세히 알아보기
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카탈로그 번호
VolumeMetric
11203D
11204D
2 개 옵션
카탈로그 번호 11203D
제품 가격(KRW)
691,000
キャンペーン価格
Ends: 31-Dec-2025
767,000
할인액 76,000 (10%)
Each
카트에 추가하기
제품 가격(KRW)
691,000
キャンペーン価格
Ends: 31-Dec-2025
767,000
할인액 76,000 (10%)
Each
카트에 추가하기
Dynabeads™ Sheep anti-Rabbit IgG는 면역글로불린 또는 다른 표적 분자를 간단하고 효율적으로 결합하게 도와주는 고형 보조제입니다. 균일하게 배치된 beads는 지름이 2.82.8 µm 이며, 양에서 분리된 anti-rabbit 폴리클로널 항체와 결합되어 있습니다. 이들 항체는 모든 종류의 rabbit IgG군들과 결합합니다. 이들 항체는 모든 토끼 IgG 하위군을 결합시킵니다.
어플리케이션
면역글로불린(Ig) 결합
단백질 정제
Sandwich immunoassay
면역침전
공동-면역침전(Co-IP)
미생물 분리
세포 제거, 음성 및 양성 분리(음성 분리 후 세포를 유세포분석에 이용가능)
다양한 어플리케이션에 사용할 수 있는 융통성있는 산물
장점:
빠른 절차와 높은 수율
편리하고 쉬운 사용
컬럼이나 원심분리 단계 불필요
이동성 자기 beads의 물리적 포획
신속하고 강하지 않은 자기 취급 절차
용출 중 항체나 펩티드 비포획
자동화에 완벽: Dynabeads™는 배치내 및 배치간 크기, 형태, 결합력이 매우 균일하여 자동화에 이상적입니다. 자기 취급 절차와 자석은 단백질 샘플의 효율적인 고속 분획화를 위해 개발되었습니다.
Dynabeads™ 소개: Dynabeads™는 균일한 구형의 단분산, 비기공 superparamagnetic bead로 여러 가지 표면 코팅에 이용할 수 있습니다. 이들은 용액에서 매우 이동성이 높아 포획 표면이 자유롭게 지속적으로 전체 샘플 용량과 상호작용할 수 있습니다. 첫 포획 후, tube를 강력한 자기장이 흐르는 거치대로 옮기면 superparamagnetic bead가 tube 벽쪽으로 당겨집니다. 강력한 자기장이 Dynabeads™를 tube 벽으로 빠르게 끌어당겨 피펫으로 상층액을 쉽고 완벽하게 빼낼 수 있게 합니다. 세척 단계도 마찬가지로 실시합니다.
For Research Use Only. Not for use in diagnostic procedures.
사양
인증/적합성ISO9001 and ISO13485
색상Brown
농도10 mg/mL
설명Polyclonal sheep anti-rabbit IgG covalently bound to Dynabeads
Dynabeads M-280 Sheep Anti-Rabbit IgG is supplied in PBS, pH 7.4 w/0.1% BSA, 0.02% NaN3 Store at 2°C to 8°C.
자주 묻는 질문(FAQ)
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.
I have a long double-stranded DNA fragment I would like to isolate. What product do you recommend?
For biotin-labeled DNA that is less than 1 kb, we recommend you use Dynabeads M270 Streptavidin (Cat. No. 65305) and MyOne C1 magnetic beads (Cat. No. 65001). We recommend our Dynabeads KilobaseBINDER Kit (Cat. No. 60101), which is designed to immobilize long (>1 kb) double-stranded DNA molecules. The KilobaseBINDER reagent consists of M-280 Streptavidin-coupled Dynabeads magnetic beads along with a patented immobilization activator in the binding solution to bind to long, biotinylated DNA molecules for isolation. Please see the following link (https://www.thermofisher.com/us/en/home/life-science/dna-rna-purification-analysis/napamisc/capture-of-biotinylated-targets/immobilisation-of-long-biotinylated-dna-fragments.html) for more information in regards to long biotinylated DNA fragment isolation.
Can I use Dynabeads magnetic beads to isolate single-stranded DNA templates?
Yes, Dynabeads magnetic beads can be used to isolate single-stranded DNA. Streptavidin Dynabeads magnetic beads can be used to target biotinylated DNA fragments, followed by denaturation of the double-stranded DNA and removal of the non-biotinylated strand. The streptavidin-coupled Dynabeads magnetic beads will not inhibit any enzymatic activity. This enables further handling and manipulation of the bead-bound DNA directly on the solid phase. Please see the following link (https://www.thermofisher.com/us/en/home/life-science/dna-rna-purification-analysis/napamisc/capture-of-biotinylated-targets/preparing-single-stranded-dna-templates.html) for more information in regards to single-stranded DNA capture.
What is the magnetic susceptibility for Dynabeads magnetic beads?
Magnetic susceptibility is a measure of how quickly the beads will migrate to the magnet. This will depend on the iron content and the character of the iron oxide. The magnetic susceptibility given for the Dynabeads magnetic beads is the mass susceptibility, given either as cgs units/g or m^3/kg (the latter being an SI unit). For ferri- and ferromagnetic substances, the magnetic mass susceptibility is dependent upon the magnetic field strength (H), as the magnetization of such substances is not a linear function of H but approaches a saturation value with increasing field. For that reason, the magnetic mass susceptibility of the Dynabeads magnetic beads is determined by a standardized procedure under fixed conditions. The magnetic mass susceptibility given in our catalog is thus the SI unit. Conversion from Gaussian (cgs, emu) units into SI units for magnetic mass susceptibility is achieved by multiplying the Gaussian factor (emu/g or cgs/g) by 4 pi x 10^-3. The resulting unit is also called the rationalized magnetic mass susceptibility, which should be distinguished from the (SI) dimensionless magnetic susceptibility unit. In general, magnetic mass susceptibility is a measure of the force (Fz) influencing an object positioned in a nonhomogenous magnetic field. The magnetic mass susceptibility of the Dynabeads magnetic beads is measured by weighing a sample, and then subjecting the sample to a magnetic field of known strength. The weight (F1) is then measured, and compared to the weight of the sample when the magnetic field is turned off (F0). The susceptibility is then calculated as K x 10^-3 = [(F1-F0) x m x 0.335 x 10^6], where K is the mass susceptibility of the sample of mass m. The susceptibility is then converted to SI units.
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