所有图片(3)
别名:
3-[2-[2-[[3-（2,5-二氢-2,5-二氧代-1H-吡咯-1-基）-1-氧代丙基]氨基]乙氧基]乙氧基]丙酸2,5-二氧代-1-吡咯烷基酯, 马来酰亚胺-PEG2-NHS
经验公式（希尔记法）:
C18H23N3O9
推荐产品
质量水平
检测方案
≥95%
形式
solid
反应适用性
reaction type: Pegylations
reagent type: cross-linking reagent
mp
92-94 °C
官能团
NHS ester
maleimide
储存温度
−20°C
SMILES字符串
O=C(N1CCC(NCCOCCOCCC(ON(C(CC2)=O)C2=O)=O)=O)C=CC1=O
InChI
1S/C18H23N3O9/c22-13(5-8-20-14(23)1-2-15(20)24)19-7-10-29-12-11-28-9-6-18(27)30-21-16(25)3-4-17(21)26/h1-2H,3-12H2,(H,19,22)
InChI key
TZPDZOJURBVWHS-UHFFFAOYSA-N
应用
具有短环氧乙烷间隔基的异双功能交联剂，用于将胺基与含巯基化合物或生物分子的连接。马来酰亚胺官能团将与巯基反应，而琥珀酰亚胺酯基团将与胺反应。间隔基长度为17.6埃。
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
Sinem K Saka et al.
Nature biotechnology, 37(9), 1080-1090 (2019-08-21)
Spatial mapping of proteins in tissues is hindered by limitations in multiplexing, sensitivity and throughput. Here we report immunostaining with signal amplification by exchange reaction (Immuno-SABER), which achieves highly multiplexed signal amplification via DNA-barcoded antibodies and orthogonal DNA concatemers generated
Sabrina Simoncelli et al.
Cell reports, 33(12), 108523-108523 (2020-12-29)
Elucidating the mechanisms that controlled T cell activation requires visualization of the spatial organization of multiple proteins on the submicron scale. Here, we use stoichiometrically accurate, multiplexed, single-molecule super-resolution microscopy (DNA-PAINT) to image the nanoscale spatial architecture of the primary inhibitor
Nirakar Basnet et al.
Nature cell biology, 20(10), 1172-1180 (2018-09-27)
Microtubules are central elements of the eukaryotic cytoskeleton that often function as part of branched networks. Current models for branching include nucleation of new microtubules from severed microtubule seeds or from γ-tubulin recruited to the side of a pre-existing microtubule.
Florian Schueder et al.
Nature communications, 8(1), 2090-2090 (2017-12-14)
Single-molecule localization microscopy (SMLM) can visualize biological targets on the nanoscale, but complex hardware is required to perform SMLM in thick samples. Here, we combine 3D DNA points accumulation for imaging in nanoscale topography (DNA-PAINT) with spinning disk confocal (SDC)
Thomas Schlichthaerle et al.
Chembiochem : a European journal of chemical biology, 20(8), 1032-1038 (2018-12-28)
Current optical super-resolution implementations are capable of resolving features spaced just a few nanometers apart. However, translating this spatial resolution to cellular targets is limited by the large size of traditionally employed primary and secondary antibody reagents. Recent advancements in
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