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GE45152105050250

SpeedBeads magnetic carboxylate modified particles

Cytiva 45152105050250, 1 μm avg. part. size, suspension (5% Solids)

别名:

SpeedBeads

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About This Item

分類程式碼代碼:
12352202
NACRES:
NA.56

ligand

(carboxylate modified particles)

形狀

suspension (5% Solids)

包裝

pkg of 15 mL

製造商／商標名

Cytiva 45152105050250

濃度

50 mg/mL

樣品平均尺寸

1 μm

運輸包裝

wet ice

儲存溫度

2-8°C

一般說明

Sera-Mag™ SpeedBeads and Sera-Mag™ Carboxylate-Modified Magnetic Particles combine a fast magnetic response time and high binding capacity with a large surface area, high sensitivity, stability, physical integrity, and fast reaction kinetics. Covalent coupling of biomolecules such as proteins and nucleic acids to carboxyl groups on the surface is easily accomplished using our standard coupling technology. The core of the particle is made by a free radical emulsion polymerization of styrene and acid monomer. One (Sera-Mag™) or two (Sera-Mag™ SpeedBeads) layers of magnetite are then coated onto this core, while the surface is modified to minimize non-specific binding of proteins.

應用

Sera-Mag™ SpeedBeads and Sera-Mag™ Carboxylate-Modified Magnetic Particles typical application uses include sample preparation, proteomics, nucleic acid isolation, and immunoassay applications.

特點和優勢

Sera-Mag™ SpeedBeads and Sera-Mag™ Carboxylate-Modified Magnetic Particles allow convenient covalent coupling of target molecules.

  • Carboxylic groups on the surface permit easy covalent coupling to biomolecules of interest using convenient carbodiimide chemistry.
  • Different levels of hydrophobicity/hydrophilicity available.
  • Available in Sera-Mag™ SpeedBeads and original Sera-Mag™ versions.
  • Excellent sensitivity and low nonspecific binding for greater accuracy.
  • Fast Magnetic Response Times and Stable Physical Integrity

儲存和穩定性

4 °C

分析報告

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

法律資訊

Sera-Mag is a trademark of Cytiva

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

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Jan Leipert et al.
Lab on a chip, 19(20), 3490-3498 (2019-09-19)
While LC-MS-based proteomics with high nanograms to micrograms of total protein has become routine, the analysis of samples derived from low cell numbers is challenged by factors such as sample losses, or difficulties encountered with the manual manipulation of small
Georg Michlits et al.
Nature methods, 14(12), 1191-1197 (2017-10-19)
Pooled CRISPR screens are a powerful tool for assessments of gene function. However, conventional analysis is based exclusively on the relative abundance of integrated single guide RNAs (sgRNAs) between populations, which does not discern distinct phenotypes and editing outcomes generated

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