N(4)-(Beta-N-Acetylglucosaminyl)-L-Asparaginase (AGA) Antibody

260€ (50 µg)
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935106861
info@markelab.com
name
N(4)-(Beta-N-Acetylglucosaminyl)-L-Asparaginase (AGA) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx377908
tested applications
ELISA, WB, IHC
Description
N(4)-(Beta-N-Acetylglucosaminyl)-L-Asparaginase (AGA) Antibody is a Rabbit polyclonal antibody for the detection of Human N(4)-(Beta-N-Acetylglucosaminyl)-L-Asparaginase (AGA).
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | Primary Antibodies |
Immunogen Target | N(4)-(Beta-N-Acetylglucosaminyl)-L-Asparaginase (AGA) |
Host | Rabbit |
Reactivity | Human |
Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | Unconjugated |
Isotype | IgG |
Size 1 | 50 µg |
Size 2 | 100 µg |
Form | Liquid |
Tested Applications | ELISA, WB, IHC |
Buffer | 0.01 M PBS, pH 7.4, 50% glycerol, 0.05% Proclin-300. |
Availability | Shipped within 5-12 working days. |
Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | P20933 |
Gene ID | 175 |
NCBI Accession | NP_000018.2 |
Background | Antibody anti-AGA |
Status | RUO |
Descripción
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Aspartylglucosylamine Deaspartylase (AGA) Antibody
AGA Antibody is a Rabbit Polyclonal antibody against AGA. 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.
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