P0709L,  PNGase F (Glycerol Free), recombinant - 75.000 units

P0709L, PNGase F (Glycerol Free), recombinant - 75.000 units

P0710S,  Rapid PNGase F - 50 reactions

P0710S, Rapid PNGase F - 50 reactions

P0709S, PNGase F (Glycerol Free), recombinant - 15.000 units

1.217,37 RON

PNGase F is the most effective enzymatic method for removing almost all N-linked oligosaccharides from glycoproteins. PNGase F (Glycerol-free), Recombinant is a recombinant amidase, which cleaves between the innermost GlcNAc and asparagine residues of high mannose, hybrid, and complex oligosaccharides. 

SKU
NEB_P0709S

PNGase F is the most effective enzymatic method for removing almost all N-linked oligosaccharides from glycoproteins. PNGase F (Glycerol-free), Recombinant is a recombinant amidase, which cleaves between the innermost GlcNAc and asparagine residues of high mannose, hybrid, and complex oligosaccharides. 

  • Recombinant enzyme; guaranteed endoglycosidase F1, F2 or F3 free
  • Glycerol-free for optimal performance in HPLC and mass spectrometry analysis
  • ≥ 95% purity, as determined by SDS-PAGE and intact ESI-MS
  • Optimal activity and stability for up to 24 months
  • Can be used under native or denaturing conditions
  • Optimized for deglycosylation of glycoproteins; leaves N-glycan core oligosaccharides intact and suitable for further analysis

 

Product Source

Cloned from Elizabethkingia miricola (formerly Flavobacterium meningosepticum) and expressed in E. coli.

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Price 1.023,00 RON (preturile sunt fara TVA)
Description

PNGase F is the most effective enzymatic method for removing almost all N-linked oligosaccharides from glycoproteins. PNGase F (Glycerol-free), Recombinant is a recombinant amidase, which cleaves between the innermost GlcNAc and asparagine residues of high mannose, hybrid, and complex oligosaccharides. 

  • Recombinant enzyme; guaranteed endoglycosidase F1, F2 or F3 free
  • Glycerol-free for optimal performance in HPLC and mass spectrometry analysis
  • ≥ 95% purity, as determined by SDS-PAGE and intact ESI-MS
  • Optimal activity and stability for up to 24 months
  • Can be used under native or denaturing conditions
  • Optimized for deglycosylation of glycoproteins; leaves N-glycan core oligosaccharides intact and suitable for further analysis

 

Product Source

Cloned from Elizabethkingia miricola (formerly Flavobacterium meningosepticum) and expressed in E. coli.