Source: Contributed by Nanci Donacki Date Added: 2002-05-14 Date Modified: 2004-04-28 Reagents and Materials -
PBS -
PBS: 0.05M EDTA -
PBS: 0.01% thimerosal -
Conjugate Storage Buffer -
SATA -
DMF -
Hydroxylamine hydrochloride -
NaOH Pellets -
PD10 Column or Sephadex G25 -
Sulfo-SMCC Preparation of Thiolated Antibody -
Concentrate the antibody to 5-7 mg/ml -
Dissolve 10 mg of SATA in 1 ml DMF (SATA:DMF) -
Add 3.0 æl SATA:DMF per mg of antibody -
Gently stir solution for 2 hours at room temperature. -
Dissolve 0.5 g hydroxylamine hydrochloride in 10 ml PBS:EDTA -
Add 0.25 g NaOH pellets to this solution to neutralize to approximately pH 7.0 -
Add to antibody solution at 6.49 æl/æl SATA. -
Gently stir for 30 minutes at room temperature. -
Equilibrate column with PBS:EDTA. -
Desalt thiolated antibody on column. Collect in the smallest volume possible without collecting any SATA. Allow free SATA (2nd peak) to come off the column. -
Store the thiolated antibody at 2-8oC for no more than one hour. -
Re-equilibrate the column with PBS. Preparation of Maleimide:HRP -
Weigh out 1.067 mg HRP for each mg of thiolated antibody. -
Add 1.1 mg Sulfo-SMCC per mg of HRP -
Add PBS to a final concentration of 8 mg/ml HRP -
Mix for 2 hours on a rotator. -
Desalt the HRP on PBS equilibrated column. Collect the first peak. Preparation of Ab:HRP Conjugate -
Immediately mix the HRP with the thiolated antibody at 1 mg HRP per mg antibody. -
Gently stir for 16-20 hours at 2-8oC. -
Dialyze against 3 changed of PBS, changing every 2 hours, 100X the conjugate volume. -
Dilute the conjugate 2-fold in Conjugate Storage Buffer. Sterile Filter. Protocol Online
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