AGA anticorps
-
- Antigène Voir toutes AGA Anticorps
- AGA (Aspartylglucosaminidase (AGA))
-
Reactivité
- Humain
-
Hôte
- Lapin
-
Clonalité
- Polyclonal
-
Conjugué
- Cet anticorp AGA est non-conjugé
-
Application
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Antigen affinity purification
- Immunogène
- Fusion protein of Human AGA
- Isotype
- IgG
-
anti-Aspartylglucosaminidase (AGA) (AA 28-245) antibody
AGA Reactivité: Humain WB, IHC, IP, ICC Hôte: Lapin Polyclonal unconjugated
anti-Aspartylglucosaminidase (AGA) (AA 24-260) antibodyAGA Reactivité: Souris WB, IHC, IP, ICC Hôte: Lapin Polyclonal unconjugated
anti-Aspartylglucosaminidase (AGA) (AA 206-346) antibodyAGA Reactivité: Humain WB, ELISA Hôte: Lapin Polyclonal unconjugated
anti-Aspartylglucosaminidase (AGA) (AA 1-346) antibodyAGA Reactivité: Humain WB Hôte: Souris Polyclonal unconjugated
anti-Aspartylglucosaminidase (AGA) (AA 138-187) antibodyAGA Reactivité: Humain, Boeuf (Vache), Chien, Cobaye, Cheval, Porc WB Hôte: Lapin Polyclonal unconjugated
-
- Indications d'application
- ELISA:1:1000-1:2000, WB:1:200-1:1000, IHC:1:15-1:50,
- Restrictions
- For Research Use only
-
- Format
- Liquid
- Buffer
- -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C,-80 °C
- Stockage commentaire
- Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
-
- Antigène
- AGA (Aspartylglucosaminidase (AGA))
- Autre désignation
- AGA (AGA Produits)
- Synonymes
- anticorps AGU, anticorps ASRG, anticorps GA, anticorps AW060726, anticorps aspartylglucosaminidase, anticorps AGA, anticorps Aga
- Sujet
-
Background: Aspartylglucosaminidase 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. The lysosomal storage disease aspartylglycosaminuria is caused by a deficiency in the AGA enzyme. Alternatively spliced transcript variants have been identified.
Aliases: Aga antibody, AGU antibody, Aspartylglucosaminidase antibody, Aspartylglucosylamine deaspartylase antibody, Aspartylglycosaminuria antibody, ASPG_HUMAN antibody, ASRG antibody, GA antibody, Glycosylasparaginase antibody, Glycosylasparaginase beta chain antibody, N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase antibody, N4 (N acetyl beta glucosaminyl) L asparagine amidase antibody, N4-(N-acetyl-beta-glucosaminyl)-L-asparagine amidase antibody
- UniProt
- P20933
-
