SwePub
Sök i LIBRIS databas

  Extended search

onr:"swepub:oai:DiVA.org:uu-210119"
 

Search: onr:"swepub:oai:DiVA.org:uu-210119" > In situ generation ...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

In situ generation of IDA groups on nanoporous alumina for reversible immobilization of enzymes and other biomolecules.

Berglin, Lennart (author)
Uppsala universitet,Institutionen för kemi - BMC
Kjellander, Marcus (author)
Uppsala universitet,Institutionen för kemi - BMC
Johansson, Gunnar (author)
Uppsala universitet,Institutionen för kemi - BMC
 (creator_code:org_t)
English.
  • Other publication (other academic/artistic)
Abstract Subject headings
Close  
  • Nanoporous alumina membranes were silanized with aminopropylsilane and iminodiacetic (IDA) groups were generated in situ by reaction with iodoacetate. The membranes were mounted in standard filter holders, connected to a HPLC system and saturated with selected metal ions. Cu(II) ions allowed the capture of chicken muscle lactate dehydrogenase with such stability, repeatability and reproducibility that Michaelis-Menten kinetics could be studied. The IDA surface was stable for months and could be depleted and regenerated with metal ions multiple times without appreciable loss of capacity. The binding of lactate dehydrogenase influenced the backpressure to the extent that could be expected for a monolayer according to Poiseuilles law.

Subject headings

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Publication and Content Type

vet (subject category)
ovr (subject category)

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Search outside SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view