This is a cached page for the URL (http://cbr.med.harvard.edu/investigators/springer/lab/protocols/chunduk_elisa_icam1.html). To see the most recent version of this page, please click here.
Protocol Online is not affiliated with the authors of this page nor responsible for its content.
About Cache
Springer Lab Protocols: [SANDWICH] ELISA FOR DETECTING SECRETED ICAM-1

[SANDWICH] ELISA FOR DETECTING SECRETED ICAM-1

by Chang-Duk Jun, 04/06/99

Purpose

Materials

Procedure

  1. Diluate mAb R6.5 (or CL203) to 10 ug/ml in PBS. Add 50 ul diluted antibody to wells. Incubate 37oC for 1 h, or O/N at 4oC.
  2. Wash 4X with PBS.
  3. Block remaining protein-binding sites by adding 200 ul/well of 1%BSA in PBS. Incubate 30 min at 37oC.
  4. Wash 4X with PBS.
  5. Add 50 ul of culture supernatant containing secreted ICAM-1. Include positive control wells of purified ICAM-1 ranging from 512 ng/ml to 2 ng/ml. Incubate 30 min at 37oC.
  6. Wash 4X with PBS.
  7. Add 50 ul/well Biotinylated R6.5 diluted in 1% BSA/PBS to a final concentration of 2 ug/ml (1:1000 dilution of stock). Incubate 30 min at 37oC.
  8. Wash 4X with PBS.
  9. Add 50 ul/well HP-streptavidin diluted accoridng to manufacturers instructions. Current dilution is 1:2000 in 1% BSA/PBS. Incubate 30 min at 37oC.
  10. Wash 4X with PBS.
  11. Wash 1X with Substrate buffer without substrate.
  12. Add 200 ul/well Substrate buffer + ABTS Substrate.
  13. Incubate at room temperature until sufficient color develops.
    May be as rapid as 2 min or as long as 20 min.
  14. Read absorbance at 414 nm, blanking against negative control well.

Expected Results

We get our best curves when the maximum Abs. for the 512 ng/ml standard is <1.500, but less than 1.800.

References

(under construction)
Springer Lab | See Other Protocols