당신은 주제를 찾고 있습니까 “pierce streptavidin magnetic beads – How to Isolate Proteins and Peptides with Streptavidin Magnetic Beads“? 다음 카테고리의 웹사이트 https://chewathai27.com/you 에서 귀하의 모든 질문에 답변해 드립니다: https://chewathai27.com/you/blog. 바로 아래에서 답을 찾을 수 있습니다. 작성자 Phenomenex 이(가) 작성한 기사에는 조회수 4,359회 및 좋아요 21개 개의 좋아요가 있습니다.
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Phenomenex is excited to introduce streptavidin coated bioZen MagBeads. These uniform paramagnetic beads are ideal for isolating proteins and peptides in less time with a higher response.
The video will take you through the process of how to best isolate your proteins and peptides to get you desired results. First you take your biotinylated antibodies and interferences and add it to the pre-treated bioZen MagBeads, then mix and incubate. While using a magnetic stand, you will need to discard all remaining liquid. Wash with phosphate buffered saline (PBS), then make sure to repeat as needed. Add your sample to a separate well of a low-bind collection plate, add in the pre-treated MagBeads, then mix and incubate. Again, discard the liquid using a magnetic stand. Wash with PBS once more and repeat as needed. Add the elution solvent, then mix and use a magnetic stand to separate the isolated sample from the MagBeads. Finally remove your cleaned-up sample and transfer it for LC-MS analysis using a bioZen LC peptide column.
To learn more about this process or any bioZen LC and sample preparation solutions, visit www.phenomenex.com/biozen.
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Thermo Scientific Pierce Streptavidin Magnetic Beads Beads
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Pierce streptavidin magnetic beads – Sigma-Aldrich
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Thermo Scientific™ Pierce™ Streptavidin Magnetic Beads
Pierce Streptavin Magnetic Beads accelerate throughput for automated magnetic purification of biotinylated molecules.
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Pierce Streptavidin Magnetic Beads – Fisher Scientific
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What streptavidin magnetic beads are you using?
Anybody has used this beads before? And what’s the difference between Dynabeads Streptavin Magnetic Beads and Pierce™ Streptavin Magnetic …
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주제와 관련된 더 많은 사진을 참조하십시오 How to Isolate Proteins and Peptides with Streptavidin Magnetic Beads. 댓글에서 더 많은 관련 이미지를 보거나 필요한 경우 더 많은 관련 기사를 볼 수 있습니다.
주제에 대한 기사 평가 pierce streptavidin magnetic beads
- Author: Phenomenex
- Views: 조회수 4,359회
- Likes: 좋아요 21개
- Date Published: 2019. 9. 25.
- Video Url link: https://www.youtube.com/watch?v=PhFyHs0iWR8
How do you use streptavidin magnetic beads?
Aliquot 125 µl (500 µg) of Streptavidin Magnetic Beads per 100 µg of total RNA into a clean RNase-free microcentrifuge tube. Add 100 µl of Wash/Binding Buffer and vortex to suspend beads. Apply magnet to side of tube for approximately 30 seconds. Remove and discard supernatant.
Are streptavidin beads magnetic?
These streptavidin magnetic beads are validated and optimized for use with high-throughput magnetic platforms, such as the Thermo Scientific KingFisher 96 and KingFisher Flex Instruments, but the beads also enable premium performance for simple benchtop applications using an appropriate magnetic stand.
How do you elute from streptavidin beads?
To minimize streptavidin leaching, do not exceed 10 minutes for the elution step in either manual or automated protocols. Boiling the magnetic beads in SDS-PAGE reducing sample buffer is acceptable for single-use applications. Boiling will cause bead aggregation and loss of binding activity.
Can you reuse streptavidin beads?
For most applications involving dissociation of biotinylated molecules from streptavidin it is not possible to reuse the beads. The streptavidin-biotin bond is one of the strongest biological bonds known, and the conditions necessary to break this bond also destroy the streptavidin.
What are streptavidin magnetic beads?
Streptavidin Magnetic Beads are 1 µm superparamagnetic particles covalently coupled to a highly pure form of streptavidin. The beads can be used to capture biotin labeled substrates including antigens, antibodies and nucleic acids.
How do you separate biotin and streptavidin?
The biotinylated antibody-antigen complexes bind tightly to Streptavidin Sepharose and the antigen can then be eluted separately using milder elution conditions, leaving behind the biotinylated antibody.
What is the difference between NeutrAvidin and streptavidin?
Avidin, streptavidin, and neutravidin are functional and structural analogues that bind to biotin with extremely high affinity. Avidin is derived from eggs of oviparous vertebrates17, while streptavidin is derived from Streptomyces avidinii. Neutravidin is a chemically modified avidin without glycosylation.
Is biotin magnetic?
Description. Biotin Magnetic Beads are densely coated with Biotin. They are utilized in the magnetic separation and isolation of avidin-labeled proteins and nucleic acids for protein interaction studies, DNA-protein pulldowns, and purification of avidin-labeled proteins and nucleic acids.
How does biotin streptavidin work?
Avidin, Streptavidin or NeutrAvidin proteins can bind up to four biotin molecules, which are normally conjugated to an enzyme, antibody or target protein to form an Avidin-biotin complex.
How do you purify Avi protein tags?
For example, after coupling your protein onto the streptavidin beads, wash it several times with the binding buffer and heat the protein coupled beads up to 90°C in 10 mM EDTA pH 8.2 with 95% formamide for 3-5 min, this should give you a good amount of the protein.
What is streptavidin used for?
Streptavidin is widely used in Western blotting and immunoassays conjugated to some reporter molecule, such as horseradish peroxidase. Streptavidin has also been used in the developing field of Nanobiotechnology, the use of biological molecules such as proteins or lipids to create nanoscale devices/structures.
What is the difference between Neutravidin and streptavidin?
Avidin, streptavidin, and neutravidin are functional and structural analogues that bind to biotin with extremely high affinity. Avidin is derived from eggs of oviparous vertebrates17, while streptavidin is derived from Streptomyces avidinii. Neutravidin is a chemically modified avidin without glycosylation.
What is streptavidin HRP?
Streptavidin HRP conjugate is a recombinant protein purified from E. coli. It is supplied as a purified product conjugated to the enzyme horseradish peroxidase (HRP). This reagent may be used as a detection reagent for biotin-conjugated primary antibodies for immunoassay applications.
How many binding sites for biotin does streptavidin possess?
Streptavidin has four biotin binding sites, and with only two of them bound to the biotin at the terminal end of the PEO chains. The two other sites are thus free and suitable for binding other biotin functionalized molecules or proteins that can be used for assembly of more complex structures.
mRNA Isolation using Streptavidin Magnetic Beads (NEB #S1420 and NEB #S1421)
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Pierce™ Streptavidin Magnetic Beads
Thermo Scientific Pierce Streptavidin Magnetic Beads accelerate throughput for automated magnetic purification of biotinylated molecules.
Features of Streptavidin Magnetic Beads:
• High-performance beads—non-aggregating, pre-blocked, iron oxide, superparamagnetic microparticles provide exceptional uniformity for automated HTS and manual applications alike
• Stable immobilization chemistry—streptavidin is immobilized using leach-resistant chemistry
• High capacity—superior quality beads with high binding capacity provide rapid and efficient biomolecule purification from complex samples
• Low non-specific binding—stable, pre-blocked beads provide clean purification products (e.g., antigen eluted in IP with biotinylated antibody) that are compatible with mass spectrometry analysis and other downstream analyses
• Superior performance—nearly three times higher binding capacity than typical beads from other suppliers, allowing the use of smaller amounts per experiment
Applications:
• Immunoprecipitate antigens (using biotinylated antibodies) from a wide variety of sources
• Co-immunoprecipitate interaction complexes using biotinylated antibodies
• Capture protein-protein interactions in pull-down assays using biotinylated ‘bait’ proteins
• Isolate biotin-labeled DNA-protein complexes from cell or tissue extracts
• Capture single-stranded biotinylated DNA oligos
• Isolate biotinylated PCR products
These streptavidin magnetic beads are validated and optimized for use with high-throughput magnetic platforms, such as the Thermo Scientific KingFisher 96 and KingFisher Flex Instruments, but the beads also enable premium performance for simple benchtop applications using an appropriate magnetic stand. The iron oxide, super-paramagnetic particles offer superior performance (high capacity and low nonspecific binding) compared with other commercial magnetic beads.
Pierce Streptavidin Magnetic Beads use a recombinant form of streptavidin with a mass of 53kDa and a near-neutral isoelectric point (pI). The protein is a tetramer having four biotin-binding sites. Unlike avidin, streptavidin has no carbohydrate groups, resulting in low nonspecific binding. The high-affinity interaction between streptavidin and biotin cannot be dissociated efficiently except with very harsh conditions, such as boiling in sample loading buffer for SDS-PAGE or 8M guanidine·HCl, pH 1.5. Consequently, it is often possible to elute binding partners in an interaction complex without also eluting the biotinylated component.
For Research Use Only. Not for use in diagnostic procedures.
Thermo Fisher Scientific – VN
Frequently asked questions
Which Streptavidin-Coupled Dynabeads are best for my application?
This will depend on the properties of your sample, the buffers and solutions used and your downstream application. For an overview, see Invitrogen Streptavidin-Coupled Dynabeads. In general, they can all be used, but some may perform better than others in particular applications due to their characteristics. Invitrogen Dynabeads M-280 Streptavidin and Invitrogen Dynabeads MyOne Streptavidin T1 are used for both protein and nucleic acids applications. Invitrogen Dynabeads M-270 Streptavidin and Invitrogen Dynabeads MyOne Streptavidin C1 are preferred for molecular diagnostics and for handling samples with high concentration of chaotropic salt, as well as in immunoassays involving small biotinylated antigens and in applications that are not compatible with BSA as these beads are not blocked with BSA. The Dynabeads Streptavidin Trial Kit allows you to try 1 mL of all four (while supplies last). The Dynabeads MyOne Streptavidin C1/T1 offer an increased binding capacity and slower sedimentation rate, making them ideal for automated applications and/or for when larger amount of biotinylated molecules or their specific target need to be isolated.
What do M-280, M-270 or MyOne mean?
‘M’ stands for ‘magnetic’ and 280 /270 indicates the diameter of the beads. Both are 2.8 micron. M-280 denotes the hydrophobic 2.8 micron beads, while M-270 denotes the hydrophilic 2.8 micron beads. MyOne beads are 1 micron in diameter.
What is the Dynabeads kilobaseBINDER Kit?
The Invitrogen Dynabeads kilobaseBINDER Kit is designed to bind large (>2 kb) biotinylated DNA or RNA fragments. The kit contains Dynabeads M-280 Streptavidin plus a unique, patented Binding Solution. The Binding Solution enables efficient capture of long fragments of biotinylated DNA as well as small biotinylated probe hybridized with long non-biotinylated DNA.
Can I purchase the Binding Solution in the Dynabeads kilobaseBINDE Kit separately?
Currently, this buffer is only sold as part of the kit and is not available separately
How many biotin binding-sites are there per streptavidin molecule?
Streptavidin is a protein composed of four identical subunits, each containing a high affinity binding site for biotin (K D = 10 -15 M) . Streptavidin has the same biotin binding properties as avidin, but it has a low isoelectric point (pI=5) and no carbohydrate groups, resulting in low nonspecific binding.
Which buffers are recommended for immobilizing biotinylated molecules?
PBS is the recommended immobilization buffer for biotinylated proteins or other molecules. For immobilization of biotinylated nucleic acids, we recommend the following Binding and Wash (B&W): 10.0 mM Tris-HCl (pH 7.5) 1.0 mM EDTA 2.0 M NaCl.
Which Streptavidin-Coupled Dynabeads do I use to isolate RNA/DNA binding proteins?
Dynabeads M-280 Streptavidin has been extensively used for this application so this is the product we recommend.
How do I measure the binding of biotinylated molecules on streptavidin beads?
Assay the supernatant for unbound molecules. This will determine the amount of molecule bound to the Dynabeads. For nucleic acids, the concentration can be checked by OD-readings, or by running a gel. For proteins, the concentration in the supernatant can be determined by a spectrometer using a protein assay like BCA. Alternatively you can label the molecule with radioactivity or fluorescence and measure the concentration of molecule directly on the beads (former) or in the supernatant (latter).
Can the Streptavidin-Coupled Dynabeads be used directly in a PCR reaction?
Yes, the beads can be used directly in PCR, as they do not inhibit enzymatic reaction. Slight PCR-inhibition has been seen when 75–100 µg of Dynabeads M-280 Streptavidin was used in 50 µL PCR reaction, and a concentration over 100 µg per 50 µL reaction seems to inhibit PCR completely. Dynabeads M-270 Streptavidin do not show any inhibitory effect on PCR at these concentrations.
I have a dsDNA biotinylated on the beads. How can I dissociate the non-biotinylated DNA strand from the biotinylated one?
There are two methods to dissociate the non-biotinylated DNA from the biotinylated DNA strand. The following protocols are based on using 20 µL of Dynabeads Streptavidin, but are scalable. Both methods may release very small amounts of complementary biotinylated strand from streptavidin. If it is critical that no biotinylated strand is released, either adopt a different biotin modification using dual biotin (two biotin groups in sequence) or covalently bind DNA to e.g., Dynabeads M-270 Carboxylic Acid.
Using heat:
Wash the DNA coated Dynabeads in 50 µL 1 x SSC.*
Resuspend the beads in another 50 µL of 1 x SSC Incubate at 95 °C for 5 minutes.
Quickly put the tube in magnet stand for 1–2 minutes and transfer the supernatant to a new tube.
The supernatant contains your non-biotinylated DNA strand.
Using NaOH:
Wash the DNA coated Dynabeads in 50 µL 1 x SSC.*
Resuspend the beads in 20 µl of freshly prepared 0.15 M NaOH.
Incubate at room temperature for 10 minutes. Put the tube in magnet stand for 1–2 minutes and transfer the supernatant to a new tube.
The supernatant contains your non-biotinylated DNA strand. Neutralize the probe by adding 2.2 µL 10 x TE, pH 7.5 and 1.3 µL 1.25 M acetic acid.
Wash the Dynabeads coated with biotinylated strand once with 50 µL 0.1M NaOH, once with 50 µL of B&W buffer and once with 50 µL TE buffer.
*1 x SSC (0.15 M NaCl, 0.015 M sodium citrate. Dissolve the reagents in 800 mL water. Adjust pH to 7.0 with NaOH. Adjust the volume to 1 liter with water).
How do I dissociate my biotinylated molecule from Streptavidin-Coupled Dynabeads?
The streptavidin-biotin interaction is the strongest known non-covalent, biological interaction between a protein and molecule. The bond formation between biotin and avidin is very rapid and, once formed, is unaffected by wide extremes of pH, temperature, organic solvents and other denaturing agents. Unless derivative forms of biotin or modified streptavidin have been adopted for your experiment, requiring a specific form and normally gentle way to dissociate biotin from streptavidin, often very harsh methods are required to dissociate the biotin from streptavidin which will denature the streptavidin. A couple of these methods are discussed below.
Biotinylated nucleic acids:
To dissociate biotinylated nucleic acids from Streptavidin-Coupled Dynabeads, incubate the beads in 95% formamide + 10mM EDTA, pH 8.2 for 5 minutes at 65°C or for 2 minutes at 90°C. Pull the beads to the tube wall with the magnet and remove the supernatant containing the biotinylated nucleic acid from the tube. Holmberg et al. (Electrophoresis 2005, 26, 501–510), report release of biotinylated DNA from streptavidin beads after short incubation in de-ionized H 2 O but this method has not been tested by our R&D department.
Biotinylated proteins:
For biotinylated proteins, boil the beads in 0.1% SDS or SDS-PHAGE buffer for 3 min.
Are the Streptavidin-Coupled Dynabeads reusable?
For most applications involving dissociation of biotinylated molecules from streptavidin it is not possible to reuse the beads. The streptavidin-biotin bond is one of the strongest biological bonds known, and the conditions necessary to break this bond also destroy the streptavidin. However, if the Dynabeads Streptavidin have been used in applications such as isolation of DNA binding proteins and release of proteins from DNA is done by gentle methods like using high salt buffers that do not interfere with biotin-streptavidin interaction, the beads with immobilized probe may be reused.
I am using Dynabeads M-280 Streptavidin to isolate DNA binding proteins and added my biotinylated oligo to my protein sample first. I am afraid the B&W buffer could break my DNA-protein interaction?
This buffer is intended for immobilizing oligo on to the beads in the absence of protein or when the direct method is applied. For the indirect method, when the oligo is first mixed with the protein sample and Dynabeads M-280 Streptavidin are added to capture DNA-protein complex, a buffer with salt concentration as low as 150 mM should be applied. The most common methods are to use either a high salt buffer or boil the Dynabeads with DNA-protein complex in SDS sample buffer for 3–4 minutes. With a high salt buffer, a salt concentration higher than 1 M is normally applied to break DNA-protein interaction. The exact amount of salt required depends on the affinity of the protein for oligonucleotides and should be determined for each application.
How do I elute my target from biotinylated antibody without eluting the antibody off the Dynabeads?
You need to use mild elution methods like buffer with high salt (>1 M salt) or low pH. Low pH elution buffers such as 0.1 M glycine•HCl, pH 2.5–3.0 are effective for most antibody-antigen interactions. Note that boiling in SDS will also elute the antibody.
As a negative control I mixed my uncoated Streptavidin-Coupled Dynabeads with my sample but got lots of non-specific binding to the beads. Why?
When exposed to a sample consisting of different types of molecules, any solid phase matrix can interact with these molecules due to hydrophobicity, charge or other types of interactions. It is not surprising that you get non-specific binding to the beads. This method is actually used for pre-clearing of sample and is not considered a good negative control. When pre-blocked and coated with a specific molecule, beads show a lot less non-specific binding than when they are not coated. As a negative control, you could try beads that are coated with an irrelevant molecule.
Can streptavidin leak from the Streptavidin-Coupled Dynabeads?
The streptavidin molecule is covalently attached to the bead’s surface. However, not all of the four streptavidin subunits are covalently coupled to the beads, typically only one or two. Streptavidin is like other proteins; if heated it can denature and dissociate into subunits. If streptavidin-coupled Dynabeads are boiled, some of the streptavidin subunits may be released (as monomers or aggregates) from the beads. The covalently bound streptavidin subunits will not be affected by such treatment. When streptavidin is bound to biotin, the streptavidin-biotin complex is more stable than the streptavidin itself. Under normal, recommended conditions, only negligible leakage of streptavidin from the beads is detected (less than 0.2% of total attached streptavidin after 2 months at 37°C).
Thermo Scientific Pierce Streptavidin Magnetic Beads Beads; 5mL:Protein
Description
Accelerate throughput for automated magnetic purification of biotinylated molecules with Thermo Scientific™ Pierce Streptavidin Magnetic Beads.
Magnetic streptavidin beads enable affinity purification of biotin-labeled target molecules without columns or centrifugation. The platform provides a fast and convenient method for manual or automated immunoprecipitation, protein interaction analysis, DNA-protein pull-down, and purification involving biotin-labeled proteins and nucleic acids. The iron oxide superparamagnetic particles offer superior performance (high capacity and low nonspecific binding) compared with other commercial magnetic beads. Biotinylated molecules are simply added to the streptavidin-coated magnetic beads for binding. Pierce Streptavidin Magnetic Beads are validated and optimized for use with high-throughput magnetic platforms, such as the Thermo Scientific KingFisher™ 96 and KingFisher Flex Instruments, but the beads also enable premium performance for simple benchtop applications using an appropriate magnetic stand.
Highlights:
High-performance beads – non-aggregating, pre-blocked, iron oxide, superparamagnetic microparticles provide exceptional uniformity for automated HTS and manual applications alike
Stable immobilization chemistry – streptavidin is immobilized using leach-resistant chemistry
High capacity – superior quality beads with high binding capacity provide rapid and efficient biomolecule purification from complex samples
Low non-specific binding – stable, pre-blocked beads provide clean purification products (e.g., antigen eluted in IP with biotinylated antibody) that are compatible with mass spectrometry analysis and other downstream analyses
Superior performance – nearly three times higher binding capacity than typical beads from other suppliers, allowing the use of smaller amounts per experiment
Properties of Streptavidin Magnetic Beads:
Composition: ion oxide particles covalently coated with a monolayer of streptavidin protein
Magnetization: superparamagnetic (no magnetic memory)
Bead size: 1μm (nominal mean diameter)
Density: 2g/cm 3
Concentration: 10mg beads per milliliter of slurry in 0.05% sodium azide
Binding capacity: approx. 55μg biotinylated rabbit IgG per mg of beads; approx. 3500pmol biotinylated fluorescein per milliliter of beads
RNase: these bead solutions are NOT tested and certified to be RNAse-free
Requires:
Thermo Scientific KingFisher 96 or KingFisher Flex Instrument or other magnetic separator device
Recommended for:
Immunoprecipitate antigens (using biotinylated antibodies) from a wide variety of sources; Co-immunoprecipitate interaction complexes using biotinylated antibodies; Capture protein-protein interactions in pull-down assays using biotinylated bait proteins; Isolate biotin-labeled DNA-protein complexes from cell or tissue extracts; Capture single-stranded biotinylated DNA oligos; Isolate biotinylated PCR products
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Pierce™ Streptavidin Magnetic Beads, Thermo Scientific
Pierce
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Pierce™ Streptavidin Magnetic Beads, Thermo Scientific
Beads Magnetic Beads
Thermo Scientific Pierce Streptavidin Magnetic Beads accelerate throughput for automated magnetic purification of biotinylated molecules.
High-Performance Beads—non-aggregating, Pre-Blocked, Iron Oxide, Superparamagnetic Microparticles Provide Exceptional Uniformity for Automated HTS and Manual Applications Alike
Stable Immobilization Chemistry—Streptavidin is Immobilized using Leach-Resistant Chemistry
High Capacity—Superior Quality Beads with High Binding Capacity Provide Rapid and Efficient Biomolecule Purification from Complex Samples
Low Non-Specific Binding—Stable, Pre-Blocked Beads Provide Clean Purification Products (e.g., Antigen Eluted in IP with Biotinylated Antibody) that are Compatible with Mass Spectrometry Analysis and other Downstream Analyses
Superior Performance—Nearly Three Times Higher Binding Capacity than Typical Beads from other Suppliers, Allowing the use of Smaller Amounts Per Experiment
These streptavidin magnetic beads are validated and optimized for use with high-throughput magnetic platforms, such as the Thermo Scientific KingFisher 96 and KingFisher Flex Instruments, but the beads also enable premium performance for simple benchtop applications using an appropriate magnetic stand
Pierce Streptavidin Magnetic Beads use a recombinant form of streptavidin with a mass of 53kDa and a near-neutral isoelectric point (pI). The protein is a tetramer having four biotin-binding sites. Unlike avidin, streptavidin has no carbohydrate groups, resulting in low nonspecific binding. The high-affinity interaction between streptavidin and biotin cannot be dissociated efficiently except with very harsh conditions, such as boiling in sample loading buffer for SDS-PAGE or 8M guanidine∙HCl, pH 1.5. Consequently, it is often possible to elute binding partners in an interaction complex without also eluting the biotinylated component.
The iron oxide, super-paramagnetic particles offer superior performance (high capacity and low nonspecific binding) compared with other commercial magnetic beads.
Ordering information: Upon receipt store at 4?C. Product is shipped on an ice pack.
Caution: For Research Use Only. Not for use in diagnostic procedures.
pierce streptavidin magnetic beads
PureProteome Streptavidin Magnetic Beads provide researchers with a powerful bead system to help purify biotinylated molecules. This bead is suitable for immunoprecipitations, purifying nucleic acids, isolating cells and organelles.
Thermo Scientific™ Pierce™ Streptavidin Magnetic Beads from Thermo Fisher Scientific
Pierce Streptavidin Magnetic Beads use a recombinant form of streptavidin with a mass of 53kDa and a near-neutral isoelectric point (pI). The iron oxide, super-paramagnetic particles offer superior performance (high capacity and low nonspecific binding) compared with other commercial magnetic beads. Pierce streptavidin magnetic beads are validated and optimized for use with high-throughput magnetic platforms, such as the Thermo Scientific KingFisher 96 and KingFisher Flex Instruments, but the beads also enable premium performance for simple benchtop applications using an appropriate magnetic stand. The beads are ideal for immunoprecipitations, protein-protein interaction studies, and isolating biotylated PCR products.
Features:
키워드에 대한 정보 pierce streptavidin magnetic beads
다음은 Bing에서 pierce streptavidin magnetic beads 주제에 대한 검색 결과입니다. 필요한 경우 더 읽을 수 있습니다.
이 기사는 인터넷의 다양한 출처에서 편집되었습니다. 이 기사가 유용했기를 바랍니다. 이 기사가 유용하다고 생각되면 공유하십시오. 매우 감사합니다!
사람들이 주제에 대해 자주 검색하는 키워드 How to Isolate Proteins and Peptides with Streptavidin Magnetic Beads
- chromatography
- science
- proteins
- peptides
- sample preparation
- biotechnology
- MagBeads
- Phenomenex
- bioZen
- streptavidin
- antibodies
- liquid chromatgraphy
How #to #Isolate #Proteins #and #Peptides #with #Streptavidin #Magnetic #Beads
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