Goat Anti Human Fas polyclonal, antigen affinity

///Goat Anti Human Fas polyclonal, antigen affinity

Goat Anti Human Fas polyclonal, antigen affinity


accession P25445


ELISA:This antibody can be used at 2 μg/mL jointly with biotinylated Human sFas antibody to detect Human sFas. The detection limit for recombinant Human sFas is approximately 0.2 ng/well.

Western Blot:This antibody can be used at 0.2 μg/mL with the appropriate secondary reagents to detect Human sFas. The detection limit for recombinant Human sFas is approximately 0.2 ng/lane.

Source This antibody was produced in Goat immunized with recombinant Human sFas.
Species reactivity Human
Purification The specific antibody was purified from Goat sera by using immobilized recombinant Human sFas affinity chromatography.
Presentation Lyophilized from PBS, pH 7.2.
Storage The lyophilized antibody is stable for at least 1 year from date of receipt at -20° C. Upon reconstitution, this antibody can be stored in working aliquots at 2° - 8° C for one month, or at -20° C for 12 months without detectable loss of activity. Avoid repeated freeze/thaw cycles.
Usage This antibody product is for research purposes only.It may not be used for therapeutics or diagnostic purposes.

Interactor P06239
Interactor P07947
Interactor P19174
Interactor P01730 CD4_HUMAN
Interactor P06239
Interactor P12931
Interactor P19174
Interactor Q9GZQ8 MLP3B_HUMAN
Interactor Q9UER7
Interactor P48023 TNFL6_HUMAN
Interactor Q03135
Interactor Q13158
Interactor Q13546
Interactor Q14790 CASP8_HUMAN
Molecular function Calmodulin-binding
Molecular function Receptor


Sandwich ELISA

  • 96-well maxisorp plates were coated with the capture antibody overnight, then blocked with 5% FCS in PBS for 1 hour, then washed.
  • Then, the protein standard was added, and plates were incubated for 2 hrs at 37°C.
  • Plates were washed and incubated with a biotinylated detection antibody for 1 hour at 37°C.
  • After washing, plates were incubated with HRP-conjugated streptavidin for 30 min at room temperature and washed again.
  • Plates were developed using the tetramethylbenzidine peroxidase substrate system and absorbance was measured at 450-615 nm using an automated plate reader.

Western Blot

  • The Recombinant immunogen was migrated by 12% SDS-PAGE and transferred to a 0.2 um PVDF membrane.
  • After blocking the membrane in blocking buffer (5% milk powder in 20 mM Tris-HCl pH 7.5, 500 mM NaCl, 0.1% (v/v) Tween 20 , the membrane was incubated with primary antibody ( at 4°C overnight.
  • Peroxidase-linked secondary anti-rabbit were used to detect the bound primary antibodies.
  • Enhanced chemiluminescence (ECL) reagents were used to visualize