AGA Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA556736-Each-of-1 | In Stock | ₹ 52,332.00 |
PIPA556736 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 52,332.00
GST (18%): ₹ 9,419.76
Total Price: ₹ 61,751.76
Antigen
AGA
Classification
Polyclonal
Conjugate
Unconjugated
Gene
Aga
Gene Alias
Aga; AGU; Aspartylglucosaminidase; aspartylglucosylamine deaspartylase; ASRG; AW060726; GA; Glycosylasparaginase; Glycosylasparaginase alpha chain; Glycosylasparaginase beta chain; N(4)-(Beta-N-acetylglucosaminyl)-L-asparaginase; N4-(N-acetyl-beta-glucosaminyl)-L-asparagine amidase
Host Species
Rabbit
Purification Method
Antigen affinity chromatography
Regulatory Status
RUO
Gene ID (Entrez)
175
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
Immunohistochemistry
Concentration
0.2 mg/mL
Formulation
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2
Gene Accession No.
P20933
Gene Symbols
Aga
Immunogen
Recombinant protein corresponding to Human AGA
Quantity
100 μL
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- Immunogen sequence: SSPLPLVVNT WPFKNATEAA WRALASGGSA LDAVESGCAM CEREQCDGSV Highest antigen sequence identity to the following orthologs: Mouse - 86%, Rat - 84%
- 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.