Mammal GFAP DTSet enzyme-linked immunoassay kit

CAT: DSEH017805;DSEH017815 Datasheet
Specification 96*5 Test;96T*15 Test
Standard Curve Range 312.5 pg/ml -20000 pg/ml
Standard Curve Gradient 7 Points/3 Folds
Number of Incubations 2
Detectable sample
Sample Volume 50 μl
Type Not Ready-to-Use
Test Duration 120min
pg/ml O.D. Average Corrected
0.00 0.0382 0.0432 0.0407
312.50 0.1370 0.1330 0.1350 0.0943
625.00 0.2351 0.2153 0.2252 0.1845
1250.00 0.3858 0.3999 0.3929 0.3522
2500.00 0.7650 0.7750 0.7700 0.7293
5000.00 1.5470 1.5810 1.5640 1.5233
10000.00 2.9470 2.8550 2.9010 2.8603
20000.00 4.3648 4.5576 4.4612 4.4205

Product Features

  • Optimized capture and detection antibody pairings with recommended concentrations save lengthy development time
  • Development protocols are provided to guide further assay optimization
  • Assay can be customized to your specific needs
  • Economical alternative to complete kits

Kit Content

  • Capture Antibody
  • Detection Antibody
  • Recombinant Standard
  • Streptavidin conjugated to horseradish-peroxidase (Streptavidin-HRP)

Other Reagents Required

DTSet Ancillary Reagent Kit (5 plates): containing 96 well microplates, plate sealers, substrate solution, stop solution, plate coating buffer (PBS), wash buffer, and assay buffer.

  • 96 well microplates: YOUKE Life, Catalog # DSEP01. Plate Sealers: YOUKE Life, Catalog # DSSF01.
  • Coating Buffer: 137 mM NaCl, 2.7 mM KCl, 8.1 mM Na2HPO4, 1.5 mM KH2PO4, pH 7.2-7.4, 0.2μm filtered . YOUKE Life, Catalog # DSCB01.
  • Blocking Buffer: YOUKE Life, Catalog # DSBB01.
  • Wash Buffer: 0.05% Tween® 20 in PBS, pH 7.2-7.4. YOUKE Life, Catalog # DSWB01.
  • Assay Buffer: 0.5% BSA,0.05% Tween® 20,PBS Solution.YOUKE Life, Catalog # DSAB01
  • Substrate Solution: Tetramethylbenzidine. YOUKE Life, Catalog # DSTS01.
  • Stop Solution: 0.5mol/ml H2SO4. YOUKE Life, Catalog # DSSS01.

Background: GFAP

GFAP (Glial fibrillary acidic protein) is a type III intermediate filament protein. It is the major component of astrocyte intermediate filament. Defects in GFAP are a cause of Alexander disease. Alexander disease is a rare disorder of the central nervous system. It is a progressive leukoencephalopathy whose hallmark is the widespread accumulation of Rosenthal fibers which are cytoplasmic inclusions in astrocytes. At the amino acid sequence level, human GFAP shares 91% and 90% identity with rat and mouse GFAP, respectively.

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