Dynabeads™ M-280 Sheep Anti-Rabbit IgG
Dynabeads™ M-280 Sheep Anti-Rabbit IgG
Invitrogen™

Dynabeads™ M-280 Sheep Anti-Rabbit IgG

Dynabeads™ヒツジ 抗-ウサギIgGは、簡単にまた効果的に免疫グロブリン(Ig)あるいは他のターゲット分子を結合することを可能にします。 どのバッチでも均一な2.8μμm粒径のビーズ が、アフィニティ精製されたヒツジ抗-ウサギのポリクロナール抗体と共有結合します詳細を見る
製品番号(カタログ番号)VolumeMetric
11204D
11203D
製品番号(カタログ番号) 11204D
価格(JPY)
-
見積もりを依頼する
Dynabeads™ヒツジ 抗-ウサギIgGは、簡単にまた効果的に免疫グロブリン(Ig)あるいは他のターゲット分子を結合することを可能にします。 どのバッチでも均一な2.8μμm粒径のビーズ が、アフィニティ精製されたヒツジ抗-ウサギのポリクロナール抗体と共有結合します。 これら抗体が全てのウサギIgGサブクラスに結合します。

アプリケーション
  • 免疫グロブリン(Ig)の結合
  • タンパク質精製
  • サンドイッチ免疫測定
  • 免疫沈降
  • 共免疫沈降(Co-IP)
  • 微生物の分離
  • 細胞枯渇、ネガティブおよびポジティブ分離(ネガティブ分離後、細胞はフローサイトメトリーに適応)
  • 様々なアプリケーションに対応する柔軟な製品

長所:
  • 手順が素早く、高い回復
  • 便利で簡単な使用方法カラムや調整の必要なし流動性のある磁気ビーズで物理吸着
  • 迅速かつ穏やかな磁気による方法溶離中に抗体または
  • ペプチドを捕らえません

自動化に最適:
Dynabeads™は、バッチ内バッチ間共に、均一なサイズ、またシャープな結合能力が非常に一貫しており、自動化に最適です。 磁気による手法と磁石は、タンパク質サンプルの分離において高効率で極度なハイスループットのために設計されています。

Dynabeadsの特徴™:
Dynabeads™は均一球状な単分散の無孔の超常磁性ビーズであり、様々な表面コーティングを施された製品がございます。 水溶液内で高い分散性があり、吸着表面が自由かつ連続的にサンプル全体と接触することが可能です。 最初の吸着後、チューブを強力磁界を有すラックに移動させる事で、磁気ビーズはチューブ壁面に引き寄せられます(Dynal Magnetsを参照ください)。 強力な磁界が素早くDynabeads™をチューブ壁面に引きつけるので、簡単かつ完璧にペプチドによる上清の除去ができます。 洗浄ステップも同様に行えます。
研究用途にのみご使用ください。診断目的には使用できません。
仕様
認証/コンプライアンスISO9001 and ISO13485
Brown
濃度10 mg/mL
概要Polyclonal sheep anti-rabbit IgG covalently bound to Dynabeads
直径(メートル法)2.8 μm
使用対象(アプリケーション)Protein Purification
使用対象 (装置)KingFisher™ Sample Purification Systems, DynaMag™ Magnets
高スループット適合性High-throughput Compatible
リガンドタイプ抗体
材料ポリスチレン
純度または品質グレード研究グレード
数量10 mL
反応性Binds all rabbit IgG's
規制状況For Research Use Only
品質保持期間製造日から36カ月
出荷条件Ambient temperature
ヒツジ
ターゲットProteins
均一性Monosized 2.8 μm (CV <5%)
タイプ抗体コーティングビーズ
Unit SizeEach
組成および保存条件
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.

よくあるご質問(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.

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

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.

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

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.

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

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.

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

引用および参考文献 (4)

引用および参考文献
Abstract
CTCF binds the proximal exonic region of hTERT and inhibits its transcription.
Authors:Renaud S, Loukinov D, Bosman FT, Lobanenkov V, Benhattar J,
Journal:Nucleic Acids Res
PubMed ID:16326864
The expression of the catalytic subunit (hTERT) represents the limiting factor for telomerase activity. Previously, we detected a transcriptional repressor effect of the proximal exonic region (first two exons) of the hTERT gene. To better understand the mechanism involved and to identify a potential repressor, we further characterized this region. ... More
Heparan sulfate degradation products can associate with oxidized proteins and proteasomes.
Authors:Mani K, Cheng F, Fransson LA,
Journal:J Biol Chem
PubMed ID:17540770
The S-nitrosylated proteoglycan glypican-1 recycles via endosomes where its heparan sulfate chains are degraded into anhydromannose-containing saccharides by NO-catalyzed deaminative cleavage. Because heparan sulfate chains can be associated with intracellular protein aggregates, glypican-1 autoprocessing may be involved in the clearance of misfolded recycling proteins. Here we have arrested and then ... More
The heme activator protein Hap1 represses transcription by a heme-independent mechanism in Saccharomyces cerevisiae.
Authors:Hon T, Lee HC, Hu Z, Iyer VR, Zhang L,
Journal:Genetics
PubMed ID:15654089
The yeast heme activator protein Hap1 binds to DNA and activates transcription of genes encoding functions required for respiration and for controlling oxidative damage, in response to heme. Hap1 contains a DNA-binding domain with a C6 zinc cluster motif, a coiled-coil dimerization element, typical of the members of the yeast ... More
The luminal Vps10p domain of sortilin plays the predominant role in targeting to insulin-responsive Glut4-containing vesicles.
Authors:Shi J, Kandror KV,
Journal:J Biol Chem
PubMed ID:17220298
In fat and skeletal muscle cells, insulin-responsive vesicles, or IRVs, deliver glucose transporter Glut4 and several associated proteins to the plasma membrane in response to hormonal stimulation. Although the protein composition of the IRVs is well studied, the mechanism of their formation is unknown. It is believed, however, that the ... More