catalog number :
MBS037805
products type :
ELISA Kit
products full name :
Porcine N-Acetyl-beta-D-Glucosaminidase ELISA Kit
products short name :
N-Acetyl-beta-D-Glucosaminidase
other names :
N-acetyl-beta-D-glucosaminidase
specificity :
No significant cross-reactivity or interference between Porcine NAG and analogues was observed.
storage stability :
Store all reagents at 2-8 degree C
other info1 :
Samples: Serum, Plasma, Tissue Homogenate, Feces, Urine and Body Fluids. Assay Type: Sandwich. Detection Range: 3.12 U/L - 100 U/L. Sensitivity: 1.0 U/L.
other info2 :
Intended Uses: This Quantitative Sandwich ELISA kit is only for in vitro research use only, not for drug, household, therapeutic or diagnostic applications! It is intended to be determinated NAG concentrations in Porcine serum, plasma and other body fluids. Using Purified Porcine NAG antibody to coat Microelisa Stripplate wells to make solid-phase antibody, then add NAG and NAG antibody which has been labeled with HRP to wells, then the reactants become antibody-antigen-antibody-enzyme complex, after washing completely, add TMB substrate solution, TMB substrate becomes blue color under HRP enzyme-catalyzed, reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. The concentration of NAG in the samples is then determined by comparing the O.D. of the samples to the standard curve. Intra-assay Precision: Intra-assay CV (%) is less than 15%. Inter-assay Precision: Inter-assay CV (%) is less than 15%. [CV(%) = SD/mean x100]
products description :
Background/Introduction: This Quantitative Sandwich ELISA kit is only for in vitro research use only, not for drug, household, therapeutic or diagnostic applications! It is intended to be determinated NAG concentrations in Porcine serum, plasma and other body fluids. Using Purified Porcine NAG antibody to coat Microelisa Stripplate wells to make solid-phase antibody, then add NAG and NAG antibody which has been labeled with HRP to wells, then the reactants become antibody-antigen-antibody-enzyme complex, after washing completely, add TMB substrate solution, TMB substrate becomes blue color under HRP enzyme-catalyzed, reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm. The concentration of NAG in the samples is then determined by comparing the O.D. of the samples to the standard curve.
ncbi acc num :
AAS02154.1