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B0519

Sigma-Aldrich

Biotin−Agarose

PBS suspension

Sinónimos:

Vitamin H Agarose

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About This Item

Número MDL:
Código UNSPSC:
41106500
NACRES:
NA.56
En este momento no podemos mostrarle ni los precios ni la disponibilidad

Formulario

PBS suspension

Nivel de calidad

Extensión del etiquetado

≥30 mg avidin per mL packed resin
2-6 μmol per mL

Matriz

4% beaded agarose

activación de la matriz

epoxy

unión a la matriz

carboxy (amide linkage); resin remains relatively uncharged over wide pH range

espaciador de matriz

13 atoms

aplicaciones

life science and biopharma

temp. de almacenamiento

2-8°C

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Aplicación

Biotin contains a high affinity for binding to avidin or streptavidin. It has been widely used in biochemistry and molecular biology for detecting and labeling proteins.

Forma física

Suspension in phosphate buffered saline containing 0.02% sodium azide

Código de clase de almacenamiento

10 - Combustible liquids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Dietmar Eberbeck et al.
Journal of nanobiotechnology, 6, 4-4 (2008-03-13)
The binding reaction of the biomolecules streptavidin and anti-biotin antibody, both labelled by magnetic nanoparticles (MNP), to biotin coated on agarose beads, was quantified by magnetorelaxometry (MRX). Highly sensitive SQUID-based MRX revealed the immobilization of the MNP caused by the
Biotinylated CdSe/ZnSe nanocrystals for specific fluorescent labeling.
Charvet, N., et al.
Journal of Materials Chemistry, 14, 2638-2642 (2004)
P A Smith et al.
Nucleic acids research, 26(6), 1414-1420 (1998-04-29)
The high affinity binding interaction of biotin to avidin or streptavidin has been used widely in biochemistry and molecular biology, often in sensitive protein detection or protein capture applications. However, in vitro chemical techniques for protein biotinylation are not always
Emrah Celik et al.
Journal of molecular recognition : JMR, 25(1), 53-56 (2012-01-04)
Sample-probe contact duration (dwell time) and loading force are two important parameters for the atomic force microscopy (AFM) force spectroscopy measurements of ligand-receptor interaction. A prolonged contact time may be required to initiate ligand-receptor binding as a result of slow
A P Sibler et al.
Journal of immunological methods, 224(1-2), 129-140 (1999-06-05)
In vivo biotinylation of antibody fragments with a gene fusion approach is a realistic alternative to conventional in vitro chemical labelling. We have previously reported the construction of a vector system suitable for the bacterial expression of the binding fragment

Contenido relacionado

Investigue las interacciones proteína-proteína in vitro con análisis pull-down, utilizando métodos de afinidad, pull-down con GST, TAP y co-inmunoprecipitación.

Investigue las interacciones proteína-proteína in vitro con análisis pull-down, utilizando métodos de afinidad, pull-down con GST, TAP y co-inmunoprecipitación.

Investigue las interacciones proteína-proteína in vitro con análisis pull-down, utilizando métodos de afinidad, pull-down con GST, TAP y co-inmunoprecipitación.

Investigate in vitro protein-protein interactions with pull-down assays, utilizing affinity, GST pull-down, TAP, and co-immunoprecipitation methods.

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Questions

1–3 of 3 Questions  
  1. Salve ho acquistato questo prodotto. Esiste un protocollo di massima per il suo utilizzo?

    1 answer
    1. Unfortunately, a standard protocol is not available for this product. The sample binding capacity protocol below may be helpful:
      1. Pipette 2.0 mls of resin into pre-calibrated, fritted columns and allow the resin to pack. Measure the packed volume in milliliters.
      2. Wash the resin with 5 packed volumes of 0.5 M sodium chloride.
      3. Equilibrate the resin with 25 ml packed volumes of phosphate buffered saline (PBS), product P4417. Check the pH of effluent after the wash. The pH should be 6.75 to 7.25. If necessary, equilibrate with additional 25 X packed volume.
      4. Dissolve avidin from egg white, product A9275 at 80 mg protein/ml in PBS. Check the pH and record. If necessary, adjust the pH to 6.95 to 7.05 with 0.1 N HCl.
      5. Determination of Avidin load:
      PBS 10.0 ml
      Avidin at 80 mg/ml 0.05 ml
      Mix by inversion and measure A (280 nm) versus PBS.
      6. Calculation of Avidin Load:
      [(Net Absorbance (280 nm) x 10. 05]/(0.05 x 1.54)
      7. For each ml of packed gel in the column, add 1.0 ml of the avidin solution. Allow the column gel to equilibrate in the presence of the avidin for one hour with intermittent swirling.
      8. Wash the column with 100 packed volumes of PBS. Mix each wash by inversion and measure A (280nm) versus PBS.
      Calculation of wash:
      [(Net Absorbance (280nm) x 100] / (1.54)
      9. Bound avidin to biotin agarose= mg of avidin labeled - total avidin in wash (unbound).
      10. Binding capacity = (Bound avidin to biotin-agarose)/ml of packed gel.

      Additional references and general protocols are also available at the links provided below:
      https://www.sigmaaldrich.com/search/b0519?focus=papers&page=1&perpage=30&sort=relevance&term=B0519&type=citation_search
      https://www.sigmaaldrich.com/applications/protein-biology/protein-pulldown

      Helpful?

  2. Could you provide the protocol for this product?

    Could you provide the protocol for this product?

    1 answer
    1. Helpful?

  3. Is there a protocol available for this product?

    1 answer
    1. Unfortunately, there is no in-house protocol available for this product.

      Helpful?

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