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MilliporeSigma

C9142

Sigma-Aldrich

Cyanogen bromide-activated-Sepharose 4B

lyophilized powder

Sinónimos:

Cyanogen bromide-activated Agarose

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1 G
$150.00
5 G
$445.00

$150.00


Disponible para envío el07 de abril de 2025Detalles


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1 G
$150.00
5 G
$445.00

About This Item

Número de CAS:
Número MDL:
Código UNSPSC:
41106500
NACRES:
NA.56

$150.00


Disponible para envío el07 de abril de 2025Detalles


Solicitar un pedido a granel

Formulario

lyophilized powder

técnicas

affinity chromatography: suitable

Matriz

Sepharose 4B

grupo activo de la matriz

cyanate or related structures

espaciador de matriz

1 atom (when ligands are coupled via isourea derivative or related linkage)

hinchazón

1 g swells to 4-5 mL

tamaño de partícula

45—165 μm

temp. de almacenamiento

2-8°C

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Descripción general

Cyanogen bromide-activated-Sepharose is suitable for use in affinity chromatography and protein chromatography. It has been used to discover insecticidal agents, raise polyclonal antibodies against yeast invertase glycosyls, and study immunological processes of xenograft rejection.

C9142-15G′s updated product number is GE17-0430-01

Aplicación

Cyanogen bromide-activated-Sepharose 4B has been used:
  • in the purification of clusterin from serum by an immunoaffinity-based separation procedure
  • in affinity chromatography to isolate Leishmania donovani protein antigens from the urine of visceral leishmaniasis patients
  • in affinity chromatography for the isolation of haptoglobin from human serum

Forma física

Lyophilized powder stabilized with lactose and dextran

Información legal

Sepharose is a trademark of Cytiva

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Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable

Equipo de protección personal

Eyeshields, Gloves, type N95 (US)


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Dana A Massuto et al.
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Kevin K Takaki et al.
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Schistosome eggs provoke the formation of granulomas, organized immune aggregates, around them. For the host, the granulomatous response can be both protective and pathological. Granulomas are also postulated to facilitate egg extrusion through the gut lumen, a necessary step for
Maia Dorsett et al.
Molecular and cellular biology, 29(22), 6128-6139 (2009-09-16)
During normal development as well as in diseased states such as cancer, extracellular "niches" often provide cues to proximal cells and activate intracellular pathways. Activation of such signaling pathways in turn instructs cellular proliferation and differentiation. In the Caenorhabditis elegans
Yan Ling et al.
The Journal of biological chemistry, 282(42), 30804-30816 (2007-08-29)
Farnesyl-diphosphate synthase (FPPS) catalyzes the synthesis of farnesyl diphosphate, an important precursor of sterols, dolichols, ubiquinones, and prenylated proteins. We report the cloning and characterization of two Toxoplasma gondii farnesyl-diphosphate synthase (TgFPPS) homologs. A single genetic locus produces two transcripts
Hans Gaus et al.
Biochemistry, 57(14), 2061-2064 (2018-03-29)
The Stabilin receptors are systemic clearance receptors for some classes of chemically modified nucleic acid therapeutics. In this study, the recombinant human secreted ecto-domain of the small isoform of Stabilin-2 (s190) was purified from cell culture and evaluated for direct

Questions

1–7 of 7 Questions  
  1. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

      Helpful?

  2. After I've washed and prepared the resin in Product C9142, Cyanogen bromide-activated-Sepharose®, for the coupling reaction, how long can I wait before coupling the ligand to the resin?

    1 answer
    1. We would recommend coupling the ligand immediately after washing and preparing the resin.  This is because the reactive groups hydrolyze in the basic solution conditions of the preparation steps.  The solutions used in the coupling reaction should also be kept cold (2-8°C) during the procedure.

      Helpful?

  3. Should I use a desiccator environment for storage of Cyanogen bromide-activated-Sepharose®?

    1 answer
    1. It is a good idea to store the CNBr-activated agarose products in as dry an environment as possible, because the reactive groups are very moisture-sensitive.

      Helpful?

  4. How are proteins attached to the Cyanogen bromide-activated Sepharose® in Product C9142?

    1 answer
    1. Coupling of molecules to CNBr-activated Sepharose® is usually via amine groups.  In the case of proteins, this usually means the epsilon amines (exocyclic amines) of lysine groups.

      Helpful?

  5. What kind of volume should I use for my ligand to couple to the Cyanogen bromide-activated Sepharose®, Product C9142?

    1 answer
    1. It is best that the coupling ligand should not be in too dilute a solution.  In general, a volume ratio of 0.5 to 1 of coupling solution to CNBr-activated Sepharose® is recommended.

      Helpful?

  6. When using Product C9142, Cyanogen bromide-activated-Sepharose®, is there a particular storage buffer that I should use after I've coupled my ligand to the resin?

    1 answer
    1. This depends on the particular situation, and the answer depends more on the coupled ligand than the resin itself.  The most important criterion is to choose a buffer that is not harmful to the ligand.  It is common to include 20% ethanol or preservatives like sodium azide or thimerosal (~0.02%) to inhibit potential bacterial growth.

      Helpful?

  7. My ligand is in Tris buffer.  Can I use Product C9142, Cyanogen bromide-activated-Sepharose®, with this sample?

    1 answer
    1. Because Tris is an amine-containing buffer, we do not recommend coupling of samples in Tris buffer to the CNBr-activated Sepharose®.  Tris will react with the CNBr groups and remove sites for ligand coupling.  We would not recommend use of any amine-containing buffer in the coupling reaction.  However, after the ligand has been added in the coupling reaction, then it is OK to use amine-containing buffers to block the remaining sites (e.g. ethanolamine, glycine).

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