Tetramethylrhodamine-5-maleimide - 5 mg
- Cat.Number : AS-81446
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Maleimides are among the most frequently used reagents for thiol modification. In most proteins, the sites of reactions are at cysteine residues that either are intrinsically present or result from reduction of cystines. Unlike iodoacetamides, maleimides do not react with histidines and methionines under physiological conditions. Tetramethylrhodamine-5-maleimide is widely used for thiol modifications of peptides and proteins.
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Citations
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PNAS . 2008 Mar 11 ; 105(10) 3825 | DOI : 10.1073/pnas.0709717105
- A. Bakker
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Biochim Biophys Acta. . 2011 Jun 01 ; 1808(6)1709 | DOI : 10.1016/j.bbamem.2011.02.006.
- S. Srinivasan
Amphipathic antenna of an inward rectifier K+ channel responds to changes in the inner membrane leaflet.
PNAS. . 2012 Dec 24 ; 110(2)749 | DOI : 10.1073/pnas.1217323110.
- M. Iwamoto
- S. Oiki
References
Crystal structure of monomeric actin in the ATP state. Structural basis of nucleotide-dependent actin dynamics
J Biol Chem . 2003 Sep 01 ; 278(36) 34172 | DOI : 10.1074/jbc.M303689200
- P. Graceffa
- R. Dominguez
Tyrosine decaging leads to substantial membrane trafficking during modulation of an inward rectifier potassium channel
J Gen Physiol . 2001 Feb 01 ; 117(2) 103 | DOI : 10.1085/jgp.117.2.103
- Y. Tong
- et al