Documents
901635
Poly(ethylene glycol) bis(2-pyridyl KAT)
PEG average Mn 10,000
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form
powder or solid
mol wt
PEG average Mn 10,000
PEG ~10,000 Da
color
off-white to pale yellow
storage temp.
2-8°C
Related Categories
1 of 4
This Item | 901642 | 901645 | 900933 |
|---|---|---|---|
| mol wt PEG average Mn 10,000, PEG ~10,000 Da | mol wt PEG average Mn 10,000, PEG ~10,000 Da | mol wt PEG average Mn 20,000, PEG ~20,000 Da | mol wt Mn 13500-16500 by GPC, average Mn 15,000 |
| storage temp. 2-8°C | storage temp. 2-8°C | storage temp. 2-8°C | storage temp. −20°C |
| color off-white to pale yellow | color off-white to pale yellow | color off-white to pale yellow | color white to off-white |
General description
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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Articles
The CRISPR/Cas9 system has recently emerged as a highly specific, efficient, and versatile gene editing technology that can be utilized to build disease models and correct diseased genes. Safe and effective delivery vectors for the CRISPR/Cas9 system are in critical need to enable clinical development and future applications of CRISPR/Cas9 systems. Professor Yang Liu summarizes recent progress in nonviral nanoparticle approaches for CRISPR/Cas9 delivery.
Related Content
The Bode Group aims to develop new reactions and reagents for the synthesis of complex molecules. The Bode Group has developed N-mesityl-substituted NHCs as organocatalysts for the catalytic generation of reactive species including activated carboxylates, homoenolates, and enolates. These novel catalysts and reactions have made possible a new generation of highly enantioselective annulations from simple starting materials under mild reaction conditions, usually at room temperature and without added reagents. Furthering the goal of designing new reagents to enable the assembly of complex molecules, the Bode group has developed SnAP reagents for the facile, one-pot conversion of aldehydes into N-unprotected, saturated N-heterocycles, including bicyclic and spirocyclic structures. These easy to handle reagents provide a simple and robust alternative to the challenging and restrictive cross-coupling methods for the functionalization of saturated N-heterocycles.
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