GLA ELISA Kit
Quick Overview for GLA ELISA Kit (ABIN8055809)
Target
See all GLA ELISA KitsBinding Specificity
Reactivity
Detection Method
Method Type
Detection Range
Application
Sample Type
-
-
Minimum Detection Limit
- 93.7 pg/mL
-
Purpose
- Sandwich Human GLA Kit to quantitate Human GLA in cell culture supernatants, serum and plasma (heparin, EDTA).
-
Analytical Method
- Quantitative
-
Specificity
-
Expression system for standard: NS0
Immunogen sequence: M1-L429Capture antibody and Detection antibody: a monoclonal antibody from mouse|a biotinylated polyclonal antibody from goat
-
Cross-Reactivity (Details)
- There is no detectable cross-reactivity with other relevant proteins.
-
Sensitivity
- < 10 pg/mL
-
Components
-
- Pre-coated 96-well strip microplate
- Standard
- Biotinylated antibody (100x)
- Avidin-Biotin-Peroxidase Complex (100x)
- Sample Diluent
- Antibody Diluent
- Avidin-Biotin-Peroxidase Diluent
- Color Developing Reagent (TMB)
- Stop Solution
- Wash Buffer (25x)
- Adhesive plate sealers
-
Material not included
- Microplate Reader capable of reading absorbance at 450nm. Incubator. Automated plate washer (optional). Pipettes and pipette tips capable of precisely dispensing 0.5 μL through 1 mL volumes of aqueous solutions. Multichannel pipettes are recommended for large amount of samples. Deionized or distilled water. 500 mL graduated cylinders. Test tubes for dilution.
-
-
-
-
Application Notes
- Before using Kit, spin tubes and bring down all components to bottom of tube. Duplicate well assay was recommended for both standard and sample testing.
-
Sample Volume
- 100 μL
-
Plate
- Pre-coated
-
Protocol
- ELISA Kit is based on standard sandwich enzyme-linked immune-sorbent assay technology. An antibody has been precoated onto 96-well plates. Standards and test samples are added to the wells, a biotinylated detection antibody specific for target is added subsequently and then followed by washing with PBS or TBS buffer. Avidin-Biotin-Peroxidase Complex was added and unbound conjugates were washed away with PBS or TBS buffer. HRP substrate TMB was used to visualize HRP enzymatic reaction. TMB was catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the target amount in sample captured in plate.
-
Assay Precision
-
Intra-Assay Precision (CV%): 6.1%, 6.5%, 4.4%
Inter-Assay Precision (CV%): 4.7%, 5.4%, 5.9% -
Restrictions
- For Research Use only
-
-
-
Handling Advice
- Avoid multiple freeze-thaw cycles.
-
Storage
- 4 °C,-20 °C
-
Storage Comment
- Store at 4°C for 6 months, at -20°C for 12 months. Avoid multiple freeze-thaw cycles (Ships with gel ice, can store for up to 3 days in room temperature. Freeze upon receiving.)
-
Expiry Date
- 12 months
-
-
- GLA (Galactosidase, alpha (GLA))
-
Alternative Name
- GLA
-
Background
-
Background: 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.
Gene Full Name: galactosidase alpha
-
Gene ID
- 2717
-
UniProt
- P06280
-
Pathways
- SARS-CoV-2 Protein Interactome
Target See all GLA ELISA Kits
-