一般描述
N-羟基琥珀酰-琼脂糖™ 4 Fast Flow是一种交联预活化的基质,通过间隔臂将Sepharose 4 Fast Flow与6-氨基己酸混合获得。与N-羟基琥珀酰的酯化反应激活了末端羧基。含有配体的基直接与该活性酯相互作用,形成化学性质非常稳定的酰胺键。
应用
N-羟基琥珀酰-琼脂糖™ 4 Fast Flow已被用作基于磁颗粒的视觉检测系统的一部分,以实现扩增基因结合后的分离。它也被用来固定蛋白质在拉下试验。
特点和优势
- 特别推荐用于工艺规模应用中含氨基的小蛋白和多肽的偶联
- 高水平的预激活,这提供了所选配体的高度替代
- NHS偶联方法使配体的化学稳定附着
法律信息
Sepharose is a trademark of Cytiva
警示用语:
Danger
危险声明
危险分类
Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
3 - Flammable liquids
WGK
WGK 1
闪点(°F)
53.6 °F
闪点(°C)
12 °C
个人防护装备
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
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Porphyromonas gingivalis causes periodontal diseases and its lipopolysaccharide (LPS) is considered as a major virulence factor responsible for pathogenesis. Since initial recognition of P. gingivalis LPS (Pg.LPS) in the oral cavity might be crucial for the host response, we identified
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 805(2), 361-363 (2004-05-12)
Combinatorial phage display was used to discover peptides that selectively bind to the alpha-cobratoxin (neurotoxin) component of the multi-component venom of the Thai cobra, Naja kaouthia. Peptide sequences determined in this way were synthesized chemically and were covalently attached to
Biosensors & bioelectronics, 141, 111415-111415 (2019-06-16)
We focused on the development of a hand-held pathogen-detection device using smartphone-embedded electronic elements combined with functionalized magnetic particles (MPs) and sepharose. To perform affinity chromatography for evaluating DNA amplicons, avidin-conjugated MPs and succinimide-linked sepharose were used with biotin-primers. To
Talanta, 195, 97-102 (2019-01-11)
The current study focuses on developing a system for visually detecting an amplified bacterial (Escherichia coli O157:H7) gene using a heavy metal particle (MP) and functionalized porous sepharose gel. To functionalize DNA-specificity to the MP, an avidin-modified MP was employed
Nucleic acids research, 39(9), 3836-3851 (2011-01-20)
In Drosophila, siRNAs are classified as endo- or exo-siRNAs based on their origin. Both are processed from double-stranded RNA precursors by Dcr-2 and then loaded into the Argonaute protein Ago2. While exo-siRNAs serve to defend the cell against viruses, endo-siRNAs
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