Anti-Human ASS1 Monoclonal Antibody

ASS1 is a rate-limiting enzyme in the urea cycle. Citrullinemia type I is an autosomal recessive disorder that is caused by a deficiency of the urea cycle enzyme argininosuccinate synthetase (ASS1). Deficiency of ASS1 shows various clinical manifestations encompassing severely affected patients with fatal neonatal hyperammonemia as well as asymptomatic individuals with only a biochemical phenotype.
List Price: $455
  • Buy 5 for $432.25 each and save 5%
  • Buy 21 for $409.5 each and save 10%
  • Buy 31 for $386.75 each and save 15%
  • Buy 51 for

Properties

Data Sheet Click for Datasheet
Catalog Number MA01864
Size 100μl
Host Type Mouse
Immunogen Fusion protein of ASS1
Specificity Expressed in adult liver.1 Publication
Isotype IgG1
Reacitivity Human
Clone
Uniprot P00966
Concentration None
Dilution WB 1:1000-1:10000, IHC 1:250-1:1000, IF 1:20-1:200
Formulation
Application WB,IHC,IF,ELISA
Other Names Argininosuccinate synthase 1,Argininosuccinate synthase,Argininosuccinate synthetase 1,ASS,Ass-1,ass1,ASSA,ASSY,Citrulline aspartate ligase,Citrulline--aspartate ligase,CTLN1
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

© Copyright 2024 TZYBIOTECH. All Rights Reserved. SiteMap