• Product name
    DyLight® 488 Conjugation Kit (Fast)
  • Product overview

    Dylight ® 488 Conjugation Kit (ab201799) uses a simple and quick process to conjugate an antibody to Dylight ® 488. It can also be used to conjugate other proteins or peptides.

    To conjugate an antibody to Dylight ® 488 using this kit:
    - add modifier to antibody and incubate for 15 mins
    - add quencher and incubate for 5 mins
    The conjugated antibody can be used immediately in WB, ELISA, IHC etc. No further purification is required and 100% of the antibody is recovered for use.

    Learn about buffer compatibility below; for incompatible buffers and low antibody concentrations, use our rapid antibody purification and concentration kits. Use the FAQ to learn more about the technology, or about conjugating other proteins and peptides to Dylight ® 488.


  • Notes

    Amount and volume of antibody for conjugation to Dylight ® 488

     Kit size   Recommended 
    amount of antibody
    amount of antibody
    Maximum antibody 
    30 µg   3 x 10 µg  3 x 20 µg 3 x 10 µL
    300 µg   3 x 100 µg  3 x 200 µg 3 x 100 µL
    1 mg   1 mg 2 mg 1 mL

    Using the maximum amount of antibody may result in less labelling per antibody. 

    2 Ideal antibody concentration is 1mg/ml. 0.5 - 1 mg/ml can be used if the maximum antibody volume is not exceeded. Antibodies > 5mg/ml or < 0.5 mg/ml should be diluted /concentrated.


    Buffer Requirements for Conjugation

    Buffer should be pH 6.5-8.5.

    Compatible buffer constituents 
    If a concentration is shown, then the constituent should be no more than the concentration shown. If several constituents are close to the limit of acceptable concentration, then this can inhibit conjugation.

    50mM / 0.6% Tris1 0.1%/1% BSA2 50% glycerol
    0.1% sodium azide PBS Potassium phosphate
    Sodium chloride HEPES Sucrose
    Sodium citrate EDTA Trehalose

    1 Tris buffered saline is almost always ≤ 50 mM / 0.6%
    2 1% BSA gives lower quality conjugates, BSA can also interfere with the use of the conjugated antibody in tissue staining.

    Incompatible buffer constituents

    Thiomerosal Proclin Glycine
    Arginine Glutathione DTT

    If a constituent of the buffer containing your antibody or protein is not listed above, please check the FAQ or contact us.

    Only purified antibodies are suitable for use, ie. where other proteins, peptides, or amino acids are not present: antibodies in ascites fluid, serum or hybridoma culture media are incompatible.

    DyLight® is a trademark of Thermo Fisher Scientific Inc. and its subsidiaries.


  • Tested applications
    Suitable for: Conjugationmore details


  • Storage instructions
    Store at -20°C. Please refer to protocols.
  • Components 30 µg 300 µg 1 mg
    Dylight® 488 Conjugation Mix 3 vials 3 vials 1 vial
    Dylight® 488 Modifier Reagent 1 vial 1 vial 1 vial
    Dylight® 488 Quencher Reagent 1 vial 1 vial 1 vial
  • Research areas


Our Abpromise guarantee covers the use of ab201799 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Application Abreviews Notes
Conjugation Use at an assay dependent concentration.




This product has been referenced in:
  • Smith JP  et al. Cholecystokinin receptor antagonist alters pancreatic cancer microenvironment and increases efficacy of immune checkpoint antibody therapy in mice. Cancer Immunol Immunother 67:195-207 (2018). ICC/IF . Read more (PubMed: 29043413) »
  • Jia CE  et al. Pendrin, an anion exchanger on lung epithelial cells, could be a novel target for lipopolysaccharide-induced acute lung injury mice. Am J Transl Res 8:981-92 (2016). Read more (PubMed: 27158384) »
See all 2 Publications for this product

Customer reviews and Q&As

Excellent results

Excellent Excellent 5/5 (Ease of Use)
Dylight 488 Fast Conjugation Kit was used to label 10 µg of rat anti-TRA98 (ab82527) using Abcam's instructions.
Postnatal day 6 mouse testes were fixed with 4% paraformaldehyde. Tissue was embedded in O.C.T. and frozen. 5 micron sections were cut and transferred to slides. Sections were permeabilized with 0.1% Triton X-100 in PBS, and blocked with 3% BSA in 0.1% Triton X-100 + PBS. Sections were incubated with labeled antibody diluted to 1:25 and Alexa Fluor 555 Phalloidin at 1:500 in 3% BSA in 0.1% Triton X-100 + PBS for 1 h at RT. Sections were then washed 3X with 0.1% Triton X-100 in PBS and mounted.
TRA98 is shown in green. Phalloidin, which stains F-actin is shown in red.

Mr. Bryan Niedenberger

Verified customer

Submitted Jun 28 2016

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