Knight:Purification of His-tagged proteins/Denaturing: Difference between revisions
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This page is really just for notes purposes for [[Reshma Shetty|Reshma]]. | This page is really just for notes purposes for [[Reshma Shetty|Reshma]]. | ||
==Overview== | |||
"The high affinity of the Ni-NTA resins for 6xHis-tagged proteins or peptides is due to both the specificity of the interaction between histidine residues and immobilized nickel ions and to the strength with which these ions are held to the NTA resin." <cite>QiagenNTAManual</cite> | |||
==Safety== | |||
*Buffer A has guanidine hydrochloride in it. | |||
==References== | ==References== | ||
<biblio> | |||
#SauerDenaturingProtocol [[Sauer:Purification of His-tagged proteins/Denaturing prep]] | |||
#QiagenNTAManual [http://www1.qiagen.com/literature/handbooks/PDF/Protein/Purification/NiNTA_Spin/1023679HBNINTA_022003WW.pdf Qiagen Ni NTA Spin Kit manual] | |||
</biblio> | |||
Revision as of 11:05, 11 July 2006
In progress! If you want to purify His-tagged proteins, I recommend using Sauer:Purification of His-tagged proteins not this protocol!
This page is really just for notes purposes for Reshma.
Overview
"The high affinity of the Ni-NTA resins for 6xHis-tagged proteins or peptides is due to both the specificity of the interaction between histidine residues and immobilized nickel ions and to the strength with which these ions are held to the NTA resin." [1]
Safety
- Buffer A has guanidine hydrochloride in it.
