추천 제품
ligand
(carboxylate modified particles)
형태
suspension (5% Solids)
포장
pkg of 15 mL
제조업체/상표
Cytiva 45152105050250
농도
50 mg/mL
평균 부품 크기
1 μm
배송 상태
wet ice
저장 온도
2-8°C
관련 카테고리
일반 설명
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.
애플리케이션
Sera-Mag™ SpeedBeads and Sera-Mag™ Carboxylate-Modified Magnetic Particles typical application uses include sample preparation, proteomics, nucleic acid isolation, and immunoassay applications.
특징 및 장점
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
저장 및 안정성
4 °C
분석 메모
To view the Certificate of Analysis for this product, please visit www.cytiva.com.
법적 정보
Sera-Mag is a trademark of Cytiva
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
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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