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Reductive Amination with Tris or Ethanolamine

Dissolve the macromolecule-containing aldehydes to be blocked (i.e., a glycoprotein that has been oxidized with sodium periodate to create formyl groups) at a concentration [Pg.166]

Add 10 pi of 5 M sodium cyanoborohydride in 1N NaOH (Aldrich) per ml of the macromolecule solution volume prepared in (1). Caution Highly toxic compound. Use a fume hood and be careful to avoid skin contact with this reagent. [Pg.167]

Purify the derivatized macromolecule by dialysis or gel filtration using a buffer suitable for the nature of the substance being modified. [Pg.167]


Figure 1.124 Aldehyde groups may be blocked with Tris or ethanolamine using a reductive amination process. Figure 1.124 Aldehyde groups may be blocked with Tris or ethanolamine using a reductive amination process.

See other pages where Reductive Amination with Tris or Ethanolamine is mentioned: [Pg.166]    [Pg.155]    [Pg.135]    [Pg.166]    [Pg.155]    [Pg.135]    [Pg.801]    [Pg.493]    [Pg.473]    [Pg.172]    [Pg.355]    [Pg.393]    [Pg.348]    [Pg.348]   


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Amines Tris amine

Ethanolamines

REDUCTIVE AMINATION WITH

Tri amines

Tris , reduction

Tris amin

Tris amine

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