Mouse LYAG/GAA ELISA Kit (Colorimetric)

Novus Biologicals, part of Bio-Techne | Catalog # NBP2-82399

Novus Biologicals, part of Bio-Techne
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Key Product Details

Sample Type & Volume Required Per Well

Serum, plasma, cell supernatant, and other biological fluids (100 ul)

Sensitivity

18.75 pg/mL

Assay Range

31.25 - 2000 pg/mL

View all Lysosomal alpha-Glucosidase ELISA Kits »

Product Specifications

Assay Type

Sandwich-ELISA

Kit Type

ELISA Kit (Colorimetric)

Reactivity

Mouse

Specificity

This kit recognizes Mouse LYAG/GAA in samples. No Significant cross-reactivity or interference between Mouse LYAG/GAA and analogues was observed.

Precision

Intra-Assay Precision (Precision within an assay) CV% < 5.59

Inter-Assay Precision (Precision between assays) CV% < 5.32

Recovery for Mouse LYAG/GAA ELISA Kit (Colorimetric)

Recovery

84-103%

Linearity

Mouse LYAG/GAA ELISA Kit (Colorimetric)

Scientific Data Images for Mouse LYAG/GAA ELISA Kit (Colorimetric)

Mouse LYAG/GAA ELISA Kit (Colorimetric)

ELISA: Mouse LYAG/GAA ELISA Kit (Colorimetric) [NBP2-82399] -

ELISA: Mouse LYAG/GAA ELISA Kit (Colorimetric) [NBP2-82399] - Standard Curve Reference

Kit Contents for Mouse LYAG/GAA ELISA Kit (Colorimetric)

  • Biotinylated Detection Ab Diluent
  • Concentrated Biotinylated Detection Ab (100x)
  • Concentrated HRP Conjugate (100x)
  • Concentrated Wash Buffer (25x)
  • HRP Conjugate Diluent
  • Micro ELISA Plate (Dismountable)
  • Plate Sealer
  • Product Manual
  • Reference Standard
  • Sample Diluent
  • Stop Solution
  • Substrate Reagent

Preparation and Storage

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Storage of components varies. See protocol for specific instructions.

Background: Lysosomal alpha-Glucosidase

GAA encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq]

Long Name

Glucosidase, Alpha; Acid

Alternate Names

Acid alpha-Glucosidase, Acid Maltase, GAA, LYAG, Lysosomal alphaGlucosidase

Gene Symbol

GAA

Additional Lysosomal alpha-Glucosidase Products

Product Documents for Mouse LYAG/GAA ELISA Kit (Colorimetric)

Product Datasheets

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot number in the search box below.

Product Specific Notices for Mouse LYAG/GAA ELISA Kit (Colorimetric)

This product is for research use only and is not approved for use in humans or in clinical diagnosis. ELISA Kits are guaranteed for 6 months from date of receipt.

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