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Merck

GE17-5113-01

Streptavidin Sepharose High Performance

Cytiva 17-5113-01, pack of 5 mL

Synonym(s):

affinity chromatography medium, high performance affinity resin, biotinylated proteins purification

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About This Item

NACRES:
NA.56
UNSPSC Code:
41106500
Technical Service
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form

resin

crosslinking

cross-linked

packaging

pack of 5 mL

manufacturer/tradename

Cytiva 17-5113-01

storage condition

(20% Ethanol)

parameter

4-30 °C temp. range (working)

technique(s)

liquid chromatography (LC): suitable

matrix

highly cross-linked 6% agarose

matrix active group

Streptavidin

avg. part. size

34 μm

working range

2-10.5

capacity

>300 mg binding capacity (Biotin / mL resin), 6 mg binding capacity (biotinylated BSA / mL resin)

separation technique

affinity

storage temp.

2-8°C

General description

Streptavidin Sepharose High Performance is an affinity chromatography medium designed for fast and reliable, high resolution purification of biotinylated biomolecules.

Purified Streptavidin isolated from Streptomyces avidinii is immobilised on Sepharose High Performance. The base matrix is a rigid, highly cross-linked beaded agarose with high chemical stability. The immobilised streptavidin binds biotin and biotinylated substances through affinity chromatography.

Features and Benefits

  • Streptavidin immobilized to Sepharose High Performance for purification of biotinylated compounds
  • Extremely useful for exploiting either the strong interactions of biotin and streptavidin or the somewhat weaker interactions of 2-iminobiotin and streptavidin.
  • 34 μm bead size for improved resolution

Preparation Note

Please be aware this product may be shipped 90 days before the expiration date. For more information on the batch specific expiration date, please contact technical service.

Analysis Note

To view the Certificate of Analysis for this product, please visit www.cytiva.com.

Legal Information

Sepharose is a trademark of Cytiva


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Storage Class

3 - Flammable liquids



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Adar Hacohen et al.
Micromachines, 11(5) (2020-05-21)
The ability to manipulate and selectively position cells into patterns or distinct microenvironments is an important component of many single cell experimental methods and biological engineering applications. Although a variety of particles and cell patterning methods have been demonstrated, most
Jérôme Zervudacki et al.
The EMBO journal, 37(14) (2018-06-07)
Mobilization of transposable elements (TEs) in plants has been recognized as a driving force of evolution and adaptation, in particular by providing genes with regulatory modules that impact their transcription. In this study, we employed an ATCOPIA93 long-terminal repeat (LTR)
Song Zhu et al.
Theranostics, 11(7), 3359-3375 (2021-02-05)
Background: A metabolic "switch" from oxidative phosphorylation to glycolysis provides tumor cells with energy and biosynthetic substrates, thereby promoting tumorigenesis and malignant progression. However, the mechanisms controlling this metabolic switch in tumors is not entirely clear. Methods: Clinical specimens were