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    total-antioxidant-capacity-assay-kit-ab65329.pdf

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Total Antioxidant Capacity Assay Kit (ab65329)

  • Datasheet
  • SDS
  • Protocol Booklet
Reviews (3)Q&A (34)References (54)

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Functional studies - ab65329
  • Functional assays: TAC (ab65329)
  • Functional assays: TAC (ab65329)
  • Functional assays: TAC (ab65329)
  • Typical Trolox standard calibration curve

Key features and details

  • Assay type: Quantitative
  • Detection method: Colorimetric
  • Platform: Microplate reader
  • Assay time: 2 hr
  • Sample type: Cell culture media, Cell Lysate, Other biological fluids, Plasma, Serum, Tissue Extracts, Urine

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Overview

  • Product name

    Total Antioxidant Capacity Assay Kit
  • Detection method

    Colorimetric
  • Sample type

    Urine, Serum, Plasma, Other biological fluids, Tissue Extracts, Cell Lysate, Cell culture media
  • Assay type

    Quantitative
  • Assay time

    2h 00m
  • Product overview

    Total Antioxidant Capacity Assay Kit ab65329 can measure either the combination of both small molecule antioxidants and proteins, or small molecules alone in the presence of our proprietary Protein Mask.


    In the total antioxidant capacity assay protocol, the Cu2+ ion is converted to Cu+ by both small molecule and protein antioxidants. The Protein Mask prevents Cu2+ reduction by proteins, enabling the analysis of only the small molecule antioxidants. The reduced Cu+ ion is chelated with a colorimetric probe giving a broad absorbance peak around 570 nm, proportional to the total antioxidant capacity.


    Total antioxidant capacity assay protocol summary:
    - add protein mask to samples if only measuring small molecule total antioxidant capacity
    - add samples and standards to wells
    - add Cu2+ solution and incubate for 90 min at room temp
    - analyze with microplate reader

  • Notes

    This product is manufactured by BioVision, an Abcam company and was previously called K274 Total Antioxidant Capacity (TAC) Colorimetric Assay Kit. K274-100 is the same size as the 100 test size of ab65329.

    Antioxidants play an important role in preventing the formation of, and scavenging of, free radicals and other oxidizing species. There are three categories of antioxidant species: enzyme systems (GSH reductase, catalase, peroxidase, etc.), small molecules (ascorbate, uric acid, GSH, vitamin E, etc.) and proteins (albumin, transferrin, etc.). 

    Trolox is used to standardize antioxidants, with all other antioxidants being measured in Trolox equivalents. Measurement of the combined non-enzymatic antioxidant capacity of biological fluids and other samples provides an indication of the overall capability to counteract reactive oxygen species (ROS), resist oxidative damage and combat oxidative stress-related diseases.

    Related products

    Review the oxidative stress marker and assay guide to learn about more assays for oxidative stress.

  • Platform

    Microplate reader

Properties

  • Storage instructions

    Store at +4°C. Please refer to protocols.
  • Components Identifier 100 tests
    Assay Diluent WM 1 x 10ml
    Cu++ Reagent Blue 1 x 0.2ml
    Protein Mask NM 1 x 10ml
    Trolox Standard (1 µmol) (Lyophilized) Yellow 1 vial
  • Research areas

    • Kits/ Lysates/ Other
    • Kits
    • Cell Damage Kits
    • Oxidative stress
    • Kits/ Lysates/ Other
    • Kits
    • Cell Damage Kits
    • Cell Damage
    • Kits/ Lysates/ Other
    • Kits
    • Cell Metabolism Kits
    • Oxidative Stress Assay Kits
    • Oxidative Stress
    • Kits/ Lysates/ Other
    • Kits
    • Cell Damage Kits
    • Antioxidant
  • Relevance

    Antioxidants play an important role in preventing the formation of and scavenging of free radicals and other potentially toxic oxidizing species. There are three categories of antioxidant species: enzyme systems (GSH reductase, catalase, peroxidase, etc.), small molecules (ascorbate, uric acid, GSH, vitamin E, etc.) and proteins (albumin, transferrin, etc.). Different antioxidants vary in their reducing power, and cooperation of all different antioxidants provides greater protection against reactive oxigen or nitrogen radicals than any single compound alone. Therefore, the overall total antioxidant capacity may give more relevant biological information compared to that obtained by the measurement of individual components, as it considers the cumulative effect of all antioxidants present.

Images

  • Functional studies - ab65329
    Functional studies - ab65329Image from Wan X et al., PLoS Pathog 12(10), Fig 5D. doi: 10.1371/journal.ppat.1005954 Reproduced under the Creative Commons license http://creativecommons.org/licenses/by/4.0/

    Total antioxidant capacity was determined in mouse cardiac homogenates using Total antioxidant capacity assay kit (ab65329). 

  • Functional assays: TAC (ab65329)
    Functional assays: TAC (ab65329)

    Trolox equivalent capacity measured in milk and concentrated squash. Background signal subtracted, duplicates; +/- SD

  • Functional assays: TAC (ab65329)
    Functional assays: TAC (ab65329)

    Trolox equivalent capacity measured in mouse tissue lysates, showing quantity (nmol) per mg of extracted protein. Results following blocking of protein activity is shown (Mask). (Duplicates; +/- SD).

  • Functional assays: TAC (ab65329)
    Functional assays: TAC (ab65329)

    Trolox equivalent capacity measured in biological fluids. Results following blocking of protein activity is shown (Mask). Background signal subtracted, duplicates; +/- SD.

  • Typical Trolox standard calibration curve
    Typical Trolox standard calibration curve

Protocols

  • Protocol Booklet

Click here to view the general protocols

Datasheets and documents

  • SDS download

  • Datasheet download

    Download

References (54)

Publishing research using ab65329? Please let us know so that we can cite the reference in this datasheet.

ab65329 has been referenced in 54 publications.

  • Madariaga VI  et al. Myogenous temporomandibular disorders and salivary markers of oxidative stress-A cross-sectional study. J Oral Rehabil 48:1-9 (2021). PubMed: 32979853
  • Li M  et al. Brachyury engineers cardiac repair competent stem cells. Stem Cells Transl Med 10:385-397 (2021). PubMed: 33098750
  • Okda TM  et al. Chemopreventive and anticancer activities of indomethacin and vitamin D combination on colorectal cancer induced by 1,2-dimethylhydrazine in rats. Biomed Rep 14:27 (2021). PubMed: 33408861
  • Shili CN  et al. Effect of a Phytogenic Water Additive on Growth Performance, Blood Metabolites and Gene Expression of Amino Acid Transporters in Nursery Pigs Fed with Low-Protein/High-Carbohydrate Diets. Animals (Basel) 11:N/A (2021). PubMed: 33672517
  • D'Onofrio N  et al. Phenolic Profiles of Red Wine Relate to Vascular Endothelial Benefits Mediated by SIRT1 and SIRT6. Int J Mol Sci 22:N/A (2021). PubMed: 34073604
View all Publications for this product

Customer reviews and Q&As

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1-10 of 37 Abreviews or Q&A

Total Antioxidant Capacity Assay Kit. Mouse plasma

Excellent Excellent 5/5 (Ease of Use)
Abreviews
Abreviews
abreview image
EDTA-plasma samples from adult mouse were tested.

Protocol: Trolox standards and samples were loaded into the microplate following the manufacturer’s instructions, assayed in duplicated.
0.5 µl of sample without Protein Mask and 10 µl of sample with Protein Mask were assayed (adjust volume to 100 µl/well with ddH2O). After adding 100 µl/well of the Cu2+ working solution, the micro-plate was incubated at room temperature for 90 minutes on orbital shaker (300 rpm) protected from light. Finally, the absorbance was measured at the wavelength of 570 nm.

DR. Sergi Bayod

Verified customer

Submitted Oct 14 2021

Total antioxidant capacity kit application in rice research

Excellent Excellent 5/5 (Ease of Use)
Abreviews
Abreviews
abreview image
Plant materials
Rice plants from control and Fe stress (300 ppm Fe2+ for 3 weeks) treatments were harvested with liquid nitrogen and stored in -80 °C freezer. Rice shoot tissues were applied in the test.
Experiment procedure
Grind the rice shoot tissues to fine powder with pre-chilled pestle and mortar in liquid N. Around 50 mg of samples were weighted in 2 ml micro-centrifuge tubes and 1 ml of PBS were added to extract the total antioxidants. After 2 mins of vigorously vortex, the mixtures were placed on ice for 10 mins. Subsequently, the tubes were centrifuged at 14,000 g for 5 mins at 4 °C followed by collecting the supernatants into fresh 1.5 ml micro-centrifuge tubes. To remove the small debris, the tubes were centrifuged again at the same speed for 2 mins.
Load the trolox standards and samples to the micro-plate according to the protocol. Both standards and samples were measured with two replicates. After adding the Cu2+ reagents, the micro-plate was incubated at room temperature in dark for 90 mins. Measure the absorbance of different wells at the wavelength of 570 nm.
Results
The total antioxidant capacity (trolox equivalent) was significantly induced by the excess Fe treatment in rice shoot tissue.

additional notes: ABTRIAL-TVX7B

Abcam user community

Verified customer

Submitted Jan 24 2018

Total antioxidant capacity kit application in rice research

Excellent Excellent 5/5 (Ease of Use)
Abreviews
Abreviews
abreview image
Plant materials
Rice plants from control and Fe stress (300 ppm Fe2+ for 3 weeks) treatments were harvested with liquid nitrogen and stored in -80 °C freezer. Rice shoot tissues were applied in the test.
Experiment procedure
Grind the rice shoot tissues to fine powder with pre-chilled pestle and mortar in liquid N. Around 50 mg of samples were weighted in 2 ml micro-centrifuge tubes and 1 ml of PBS were added to extract the total antioxidants. After 2 mins of vigorously vortex, the mixtures were placed on ice for 10 mins. Subsequently, the tubes were centrifuged at 14,000 g for 5 mins at 4 °C followed by collecting the supernatants into fresh 1.5 ml micro-centrifuge tubes. To remove the small debris, the tubes were centrifuged again at the same speed for 2 mins.
Load the trolox standards and samples to the micro-plate according to the protocol. Both standards and samples were measured with two replicates. After adding the Cu2+ reagents, the micro-plate was incubated at room temperature in dark for 90 mins. Measure the absorbance of different wells at the wavelength of 570 nm.
Results
The total antioxidant capacity (trolox equivalent) was significantly induced by the excess Fe treatment in rice shoot tissue (see attached image).

Abcam user community

Verified customer

Submitted Oct 12 2017

Question

I have the method for total antioxidant capacity assay kit no-ab65329. I can’t see any info about freezer storage temps. What temp should serum be stored at. Also we’ll have samples being transported from South Africa so if they are transported on dry ice is this sufficient?

Regards

Read More

Abcam community

Verified customer

Asked on Jul 13 2012

Answer

Thank you for your enquiry.

Generally, serum can be stored at -20°C or at -70°. Freeze the tubes of serum rapidly, and store the aliquots protected from light. After thawing a tube, do not refreeze the serum unless you intend to store it for an extended period of time.

Serum stored at -20°C should be used within 6-12 months of preparation, but serum stored at -70°C may be kept longer. Normally, serum stored in a refrigerator (2-8°C) should be used within 2 weeks.

If you need any further assistance in the future, please do not hesitate to contact me.

Read More

Abcam Scientific Support

Answered on Jul 13 2012

Question

Is the Total Antioxidant Capacity Assay compatible with samples collected in glucose collection tubes? They contain sodium fluoride (antiglycolytic) and potassium oxalate (anticoagulant).

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Abcam community

Verified customer

Asked on Jun 21 2017

Answer

Plasma collected in glucose tubes will be compatible with the assay. There is no known interference from sodium fluoride or potassium oxalate.

Read More

Abcam Scientific Support

Answered on Jun 21 2017

Question

Hi, it is said on the protocol that "can use 0.05% triton solution instead of dd water if needed when prepare the samples". In which conditions triton can be a better choice?

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Abcam community

Verified customer

Asked on Dec 03 2015

Answer



The only real need for using Triton is if you are having difficulty homogenzing the cells in water, otherwise it is not necessary.



Read More

Heather Allen

Abcam Scientific Support

Answered on Dec 03 2015

Question

My question is if the kit can be used with liver, kidney, and heart of chickens.

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Abcam community

Verified customer

Asked on Oct 28 2013

Answer

Yes, the kit can be used with samples from chicken tissues. We have not generated or received chicken data but the assay is suitable for any species. For an example of data from mouse heart tissue, please see figure 4 of the following reference:

Lu D et al. Knockdown of cytochrome P450 2E1 inhibits oxidative stress and apoptosis in the cTnT(R141W) dilated cardiomyopathy transgenic mice. Hypertension 60:81-9 (2012).

http://hyper.ahajournals.org/content/60/1/81.long

Read More

Tom Ruyle

Abcam Scientific Support

Answered on Oct 28 2013

Question

What are the storage instructions for the kit?

Read More

Abcam community

Verified customer

Asked on May 30 2013

Answer

Unopened kit as received from Abcam can be stored for 6 months at 4C. Once reconstituted the standard should be stored at -20C. Please refer to the protocol booklet for further information.

Read More

Abcam Scientific Support

Answered on May 30 2013

Question

Protein mask necessary with urine sample?

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Abcam community

Verified customer

Asked on May 20 2013

Answer

If the total antioxidant capacity is desired, I would not recommend the use of the protein mask. If only the levels of the small molecule antioxidants are required, please use the protein mask.

Read More

Abcam Scientific Support

Answered on May 20 2013

Question

Dear Abcam Scientific Support Team,
I would like to check the total antioxidant capacity of the plasma samples that contain EDTA as an anticoagulant. Does the EDTA interfere with the ab65329 TAC assay?
Best regards,

Read More

Abcam community

Verified customer

Asked on Mar 04 2013

Answer

Thank you for contacting us.

Although I don’t think EDTA will have an adverse effect on the efficiency of this kit, I would not recommend using EDTA for plasma preparations. Instead use heparin or citrate.

EDTA anticoagulant will give a lower antioxidant capacity compared with heparinized plasma samples but nonetheless, sufficient for detection and data analysis.

I have included a publication mentioning the difference between EDTA and heparin anticoagulants for your reference.

The effect of anticoagulant choice on apparent total antioxidant capacity using three different methods. Ann Clin Biochem. 1995 Jul;32 ( Pt 4):413-6. http://www.ncbi.nlm.nih.gov/pubmed/7486802

I hope this information is helpful. Please do not hesitate to contact us if you require further assistance.

Read More

Abcam Scientific Support

Answered on Mar 04 2013

1-10 of 37 Abreviews or Q&A

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