alpha Galactosidase Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA129518-Each-of-1 | In Stock | ₹ 54,646.00 |
PIPA129518 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 54,646.00
GST (18%): ₹ 9,836.28
Total Price: ₹ 64,482.28
Antigen
alpha Galactosidase
Classification
Polyclonal
Conjugate
Unconjugated
Gene
GLA
Gene Alias
Agalsidase; agalsidase alfa; Ags; Alpha-D-galactosidase A; alpha-D-galactoside galactohydrolase; alpha-D-galactoside galactohydrolase 1; alpha-gal A; alpha-galactosidase A; GALA; galactosidase alpha; galactosidase, alpha; GLA; Melibiase
Host Species
Chicken
Purification Method
Ammonium sulfate precipitation
Regulatory Status
RUO
Gene ID (Entrez)
2717
Content And Storage
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Form
Liquid
Applications
ELISA, Western Blot
Concentration
1 mg/mL
Formulation
PBS with no preservative; pH 7.4
Gene Accession No.
P06280
Gene Symbols
GLA
Immunogen
Synthetic peptide- amino acids 396-407 and 55-64 of Human Galactosidase alpha.
Quantity
250 μg
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgY
Related Products
Description
- Store product as a concentrated solution
- Centrifuge briefly prior to opening the vial
- This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins
- This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose
- A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties.