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STREPMAG-RO

Roche

Streptavidin Magnetic Particles

suspension

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Synonym(s):
magnetic particles, streptavidin

form

suspension

packaging

pkg of 10 mL (11641786001)
pkg of 2 mL (11641778001)

manufacturer/tradename

Roche

shipped in

wet ice

storage temp.

2-8°C

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GE30152105010150GE30152104010350GE30152104010150
shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

2-8°C

packaging

pkg of 10 mL (11641786001), pkg of 2 mL (11641778001)

packaging

pkg of 5 mL

packaging

pkg of 100 mL

packaging

pkg of 5 mL

manufacturer/tradename

Roche

manufacturer/tradename

Cytiva 30152105010150

manufacturer/tradename

Cytiva 30152104010350

manufacturer/tradename

Cytiva 30152104010150

General description

The Streptavidin Magnetic Particles are polydisperse paramagnetic particles that are designed for the fast separation of a variety of biotin-labeled molecules. The particles are supplied in a suspension that contains 10mg particles per ml in 50mM Hepes, 0.1% bovine serum albumin (BSA), 0.01% methyl-isothiazolone, pH 7.4.

Binding capacities per mg streptavidin magnetic particles:
>=1800 pmol free biotin
>150 pmol biotin-labeled oligonucleotide
>10 pmol biotin-labeled dsDNA fragment

Application

The Streptavidin Magnetic Particles are polydisperse paramagnetic particles that are designed for the fast separation of a variety of biotin-labeled molecules. The particles are supplied in a suspension that contains 10 mg particles per ml. The magnetic separation of biotin-labeled molecules has been successfully employed in a wide range of applications.

Other Notes

For life science research only. Not for use in diagnostic procedures.

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Skin Sens. 1

Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 1

flash_point_f

No data available

flash_point_c

No data available


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Martin Schatte et al.
Bioconjugate chemistry, 27(6), 1484-1492 (2016-05-18)
Enzymes able to ligate biomolecules are emerging tools to generate site-specific bioconjugates. In this study we present a detection and screening method for bioconjugating enzymes which overcomes limitations of analytical methods such as HPLC or MS. These techniques are experimentally
Debolina Ray et al.
Cancer biology & therapy, 13(10), 848-857 (2012-07-13)
Stress treatment generally causes the post-translational modification and accumulation of the p53 protein, although the role of these aspects has not been always understood in relation to this protein's tumor suppressor activity. We analyzed these attributes of p53 in eight
Matthew T Balmer et al.
Cancer biology & therapy, 15(8), 1000-1012 (2014-05-08)
The chemotherapeutic agents doxorubicin (dox) or 5-fluorouracil (5FU) are used to treat cancer cells as they cause irreparable DNA damage, inducing these aberrant cells to undergo cell death. The mediator of this process is presumed to be in part the

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