Maurocalcine – Ion Channels and Transporters

Maurocalcine, a component of the venom of Scorpio maurus palmatus, was discovered by Michel De Waard, co-founder of Smartox. Maurocalcine folds according to an inhibitor cysteine knot. Such as Imperatoxin A, Maurocalcine acts as a high affinity agonist of the type-1 ryanodine receptor expressed in skeletal muscles with an affinity in the 10 nM range. Maurocalcine induces an increase in channel opening probability accompanied by sudden transitions to long lasting subconductance states. Maurocalcine has also been characterized as a cell penetrating peptide and its pharmacological activity can be observed upon extracellular perfusion.

 

Technical specification

 KD20 peptide Sequence : H-GDCLPHLKLCKENKDCCSKKCKRRGTNIEKRCR-OH (Cys3-Cys17; Cys10-Cys21; Cys16-Cys32)
 KD20 peptide MW : 3858.56 g/mol
 KD20 peptide Purity : > 95%
 KD20 peptide Counter-Ion : TFA Salts
Peptide library synthesis KD20 peptide Delivery format : Lyophilized

Price

 

Product Size Price €
Price $
07MAU001-0.1 mg 0.1 mg 187 € 150 $
07MAU001-0.5 mg 0.5 mg 561 € 449 $
07MAU001-1 mg 1 mg 935 € 748 $
07MAU001-
07MAU001-

If you’d like to learn more about this toxin, visit our product page on our Smartox website—Our sister company specializing in the synthesis of complex toxins.

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