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ELISA (Enzyme-Linked ImmunoadSorbent Assay)

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905

You will need the following solutions:

PBS (P hosphate-B uffered S aline, Ca/Mg free) :-

Solute 1x 10x
NaCl 8g 80g
KCl 0.2g 2g
Na2 PO4 (anhydrous) 1.15g 11.5g
KH2 PO4 (anhydrous) 0.2g 2g

    N.B.: Na2 HPO4 .2H2 O can also be used -> add 1.42g for 1x and 14.2g for 10x PBS.
    Make up to 1 litre with dd H2 O.

    PBS wash:-

    100ml 1x PBS
    10ul Tween (0.01%, final concentration)

    Citrate/Acetate Buffer pH6.0:-

    Sodium acetate - 4.1g.
    dd H2 O - 500ml.

    2. 100ml 0.1M Citric acid

    Citric acid - 2.1g.
    dd H2 O - 100ml.

    Titrate 1 with 2 to a final pH of 6.0. Citrate/Acetate Buffer, pH6 can be stored frozen at -20°C.

    • 1. 500ml 0.1M Sodium Acetate

    TMB Solution - 10mg/ml in DMSO (store at 4°C).

    The following details the method for use with TMB as the substrate (cover wells with clingfilm during incubations to prevent evaporation).

    1) Add 3ul H2 O2 to 20ml of Citrate/Acetate buffer. To every 5ml of buffer add 50ul TMB solution.
    N.B.: Colour change is from colourless to blue (yellow when acid is added).

    2) Coat plate with antigen stock solution (1ug/ml in PBS, 50ul/well) for at least 24hrs or over the weekend at 4°C or O/N at 37°C.

    3) Remove antigen and wash 3x with 1x PBS.

    4) Block with 1% BSA (100ul/well) in 1x PBS for at least 1hr at 37°C.

    5) Remove BSA by flicking plate.

    6) Wash 3x with 1x PBS containing 0.01% tween

    7) Add anti-serum (diluted as appropiate, 1/100 etc. with 1x PBS) and incubate for 2hrs @ 37°C.
    N.B.: Use positive and negative controls.

    8) Wash 4x with 1x PBS containing 0.01% tween.

    9) Add peroxidase conjugate (50ul/well) diluted 1:1000 with 1% BSA (diluted in washing solution as in 8)) and incubate for 1hr @ 37°C.
    N.B.: Use PRAM (P eroxidase-conjugated R abbit A nti-M ouse) for Ab raised in mice and PSAR (P eroxidase-conjugated S wine A nti R abbit) for Ab raised in rabbits.

    10) Wash 4x with 1x PBS containing 0.01% tween.

    11) Add substrate (100ul/well).

    12) Incubate for 1-5 mins in the dark at RT. Check reaction for colour change. Wells should turn blue.

    13) Stop reaction by the addition of 25ul 0.1M H2 SO4 /well.

    14) Read OD @ 450nm for TMB

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