Aspartylglucosylamine Deaspartylase (AGA) Antibody
195€ (20 µl)
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name
Aspartylglucosylamine Deaspartylase (AGA) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx004855
tested applications
ELISA, WB
Description
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.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Aspartylglucosylamine Deaspartylase (AGA) |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Recommended Dilution | ELISA: 1 µg/ml, WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Purified by affinity chromatography. |
| Size 1 | 20 µl |
| Size 2 | 100 µl |
| Size 3 | 2 × 100 µl |
| Form | Liquid |
| Tested Applications | ELISA, WB |
| Buffer | PBS, pH 7.3, containing 0.01% thimerosal, 50% glycerol. |
| Availability | Shipped within 5-10 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 |
| Note | Concentration: > 0.2 mg/ml - |
Descripción
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AGA antibody
Cleaves the GlcNAc-Asn bond which joins oligosaccharides to the peptide of asparagine-linked glycoproteins.
Ver Producto
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.
Ver Producto