Aga Protein Elisa

Lab Reagents

Human IgG antibody Laboratories manufactures the aga protein elisa reagents distributed by Genprice. The Aga Protein Elisa reagent is RUO (Research Use Only) to test human serum or cell culture lab samples. To purchase these products, for the MSDS, Data Sheet, protocol, storage conditions/temperature or for the concentration, please contact protein elisa. Other Aga products are available in stock. Specificity: Aga Category: Protein Group: Elisa

Elisa information

AGA siRNA
20-abx906980
  • EUR 661.20
  • EUR 878.40
  • 15 nmol
  • 30 nmol

anti-AGA
YF-PA10114 50 ul
EUR 435.6
Description: Mouse polyclonal to AGA

Human Aspartylglucosaminidase (AGA) Protein
20-abx168898
  • EUR 744.00
  • EUR 326.40
  • EUR 2264.40
  • EUR 895.20
  • EUR 543.60
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug

Mouse Aspartylglucosaminidase (AGA) Protein
20-abx168899
  • EUR 794.40
  • EUR 326.40
  • EUR 2431.20
  • EUR 944.40
  • EUR 577.20
  • 100 ug
  • 10 ug
  • 1 mg
  • 200 ug
  • 50 ug

AGA protein (His tag)
80R-4111 100 ug
EUR 392.4
Description: Recombinant Human AGA protein (His tag)

AGA Recombinant Protein (Human)
RP000700 100 ug Ask for price

AGA Recombinant Protein (Mouse)
RP114722 100 ug Ask for price

AGA Recombinant Protein (Mouse)
RP114725 100 ug Ask for price

AGA Recombinant Protein (Rat)
RP189488 100 ug Ask for price

Human Aspartylglucosaminidase(AGA)ELISA kit
201-12-2226 96 tests
EUR 528
Description: A quantitative ELISA kit for measuring Human in samples from biological fluids.

AGA ELISA Kit (Human) (OKEH07991)
OKEH07991 96 Wells
EUR 1075.2
Description: Description of target: This gene encodes a member of the N-terminal nucleophile (Ntn) hydrolase family of proteins. The encoded preproprotein is proteolytically processed to generate alpha and beta chains that comprise the mature enzyme. This enzyme is involved in the catabolism of N-linked oligosaccharides of glycoproteins. It cleaves asparagine from N-acetylglucosamines as one of the final steps in the lysosomal breakdown of glycoproteins. Mutations in this gene are associated with the lysosomal storage disease aspartylglycosaminuria that results in progressive neurodegeneration. Alternative splicing results in multiple transcript variants, at least one of which encodes an isoform that is subject to proteolytic processing.;Species reactivity: Human;Application: ELISA;Assay info: Assay Methodology: Quantitative Sandwich ELISA;Sensitivity: 0.152ng/mL

Guinea Pig AGA ELISA Kit
EGA0448 96Tests
EUR 625.2

Mouse Aspartylglucosaminidase(AGA)ELISA kit
GA-E0760MS-48T 48T
EUR 403.2

Mouse Aspartylglucosaminidase(AGA)ELISA kit
GA-E0760MS-96T 96T
EUR 640.8

Rat Aspartylglucosaminidase(AGA)ELISA kit
GA-E0842RT-48T 48T
EUR 380.4

Rat Aspartylglucosaminidase(AGA)ELISA kit
GA-E0842RT-96T 96T
EUR 595.2

Rat Aspartylglucosaminidase(AGA)ELISA kit
QY-E10810 96T
EUR 433.2