AGA Antikörper
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- Target Alle AGA Antikörper anzeigen
- AGA (Aspartylglucosaminidase (AGA))
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser AGA Antikörper ist unkonjugiert
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Applikation
- Western Blotting (WB), ELISA, Immunohistochemistry (IHC)
- Kreuzreaktivität
- Human, Maus, Ratte
- Aufreinigung
- Antigen affinity purification
- Immunogen
- Fusion protein of Human AGA
- Isotyp
- IgG
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anti-Aspartylglucosaminidase (AGA) (AA 28-245) antibody
AGA Reaktivität: Human WB, IHC, IP, ICC Wirt: Kaninchen Polyclonal unconjugated
anti-Aspartylglucosaminidase (AGA) (AA 24-260) antibodyAGA Reaktivität: Maus WB, IHC, IP, ICC Wirt: Kaninchen Polyclonal unconjugated
anti-Aspartylglucosaminidase (AGA) (AA 206-346) antibodyAGA Reaktivität: Human WB, ELISA Wirt: Kaninchen Polyclonal unconjugated
anti-Aspartylglucosaminidase (AGA) (AA 1-346) antibodyAGA Reaktivität: Human WB Wirt: Maus Polyclonal unconjugated
anti-Aspartylglucosaminidase (AGA) (AA 138-187) antibodyAGA Reaktivität: Human, Rind (Kuh), Hund, Meerschweinchen, Pferd, Schwein WB Wirt: Kaninchen Polyclonal unconjugated
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- Applikationshinweise
- ELISA:1:1000-1:2000, WB:1:200-1:1000, IHC:1:15-1:50,
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Buffer
- -20 °C, pH 7.4 PBS, 0.05 % Sodium azide, 40 % Glycerol
- Konservierungsmittel
- Sodium azide
- Vorsichtsmaßnahmen
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Lagerung
- -20 °C,-80 °C
- Informationen zur Lagerung
- Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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- Target
- AGA (Aspartylglucosaminidase (AGA))
- Andere Bezeichnung
- AGA (AGA Produkte)
- Synonyme
- AGU antikoerper, ASRG antikoerper, GA antikoerper, AW060726 antikoerper, aspartylglucosaminidase antikoerper, AGA antikoerper, Aga antikoerper
- Hintergrund
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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
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