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Hexosaminidase A ELISA Kit

Human Hexosaminidase A ELISA Kit, Colorimetric assay for quantification of Human Hexosaminidase A.
Catalog No. ABIN8055818
$499.00
Plus shipping costs $50.00
96 tests
Shipping to: United States
Delivery in 4 to 7 Business Days

Quick Overview for Hexosaminidase A ELISA Kit (ABIN8055818)

Target

See all Hexosaminidase A (HEXA) ELISA Kits
Hexosaminidase A (HEXA)

Binding Specificity

AA 1-529

Reactivity

  • 10
  • 9
  • 5
  • 2
  • 1
  • 1
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Human

Detection Method

Colorimetric

Method Type

Sandwich ELISA

Detection Range

312 pg/mL - 20000 pg/mL

Application

ELISA

Sample Type

Cell Culture Supernatant, Plasma (EDTA), Plasma (heparin), Serum
  • Minimum Detection Limit

    312 pg/mL

    Purpose

    Sandwich Human HEXA Kit to quantitate Human HEXA in cell culture supernatants, serum and plasma (heparin, EDTA).

    Analytical Method

    Quantitative

    Specificity

    Expression system for standard: NS0
    Immunogen sequence: M1-T529

    Capture 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

    < 50 pg/mL

    Components

    1. Pre-coated 96-well strip microplate
    2. Standard
    3. Biotinylated antibody (100x)
    4. Avidin-Biotin-Peroxidase Complex (100x)
    5. Sample Diluent
    6. Antibody Diluent
    7. Avidin-Biotin-Peroxidase Diluent
    8. Color Developing Reagent (TMB)
    9. Stop Solution
    10. Wash Buffer (25x)
    11. 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%): 3.9%, 5.1%, 4.8%
    Inter-Assay Precision (CV%): 5.2%, 4.5%, 5.1%

    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
  • Target See all Hexosaminidase A (HEXA) ELISA Kits

    Hexosaminidase A (HEXA)

    Alternative Name

    HEXA

    Background

    Background: Hexosaminidase A (alpha polypeptide), also known as HEXA, is an enzyme that in humans is encoded by the HEXA gene, located on the 15th chromosome. This gene encodes a member of the glycosyl hydrolase 20 family of proteins. The encoded preproprotein is proteolytically processed to generate the alpha subunit of the lysosomal enzyme beta-hexosaminidase. This enzyme, together with the cofactor GM2 activator protein, catalyzes the degradation of the ganglioside GM2, and other molecules containing terminal N-acetyl hexosamines. Mutations in this gene lead to an accumulation of GM2 ganglioside in neurons, the underlying cause of neurodegenerative disorders termed the GM2 gangliosidoses, including Tay-Sachs disease (GM2-gangliosidosis type I). Alternative splicing results in multiple transcript variants, at least one of which encodes a preproprotein that is proteolytically processed.

    Gene Full Name: hexosaminidase subunit alpha

    Gene ID

    3073

    UniProt

    P06865

    Pathways

    Sensory Perception of Sound, Glycosaminoglycan Metabolic Process
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