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    products/elisa/human-il-10-elisa-kit-high-sensitivity-ab46059.pdf

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Immunology Adaptive Immunity T Cells Non-CD
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Human IL-10 ELISA Kit High Sensitivity (ab46059)

  • Datasheet
  • SDS
  • Protocol Booklet
Submit a review Q&A (7)References (5)

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Typical Standard Curve

    Key features and details

    • Sensitivity: 1.3 pg/ml
    • Range: 1.56 pg/ml - 50 pg/ml
    • Sample type: Cell culture supernatant, Plasma, Serum
    • Detection method: Colorimetric
    • Assay type: Sandwich (quantitative)
    • Reacts with: Human

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    Overview

    • Product name

      Human IL-10 ELISA Kit High Sensitivity
      See all IL-10 kits
    • Detection method

      Colorimetric
    • Precision

      Intra-assay
      Sample n Mean SD CV%
      Overall 3 7.8%
      Inter-assay
      Sample n Mean SD CV%
      Overall 3 10.2%
    • Sample type

      Cell culture supernatant, Serum, Plasma
    • Assay type

      Sandwich (quantitative)
    • Sensitivity

      < 1.3 pg/ml
    • Range

      1.56 pg/ml - 50 pg/ml
    • Recovery

      87 %

      Sample specific recovery
      Sample type Average % Range
      Cell culture supernatant 94 % - %
      Serum 80 59% - 93%
    • Assay time

      3h 00m
    • Assay duration

      Multiple steps standard assay
    • Species reactivity

      Reacts with: Human
    • Product overview

      Abcam’s IL-10 Human High Sensitivity in vitro ELISA (Enzyme-Linked Immunosorbent Assay) kit is designed for the quantitative measurement of IL-10 in Human sera, plasmas, buffered solutions and cell culture media.


      A monoclonal antibody specific for IL-10 has been coated onto the wells of the microtiter strips provided. Samples, including standards of known IL-10 concentrations, control specimens or unknowns are pipetted into these wells. During the first incubation, the standards or samples and a biotinylated monoclonal antibody specific for IL-10 are simultaneously incubated. After washing, the enzyme Streptavidin-HRP, that binds the biotinylated antibody is added, incubated and washed. A TMB substrate solution is added which acts on the bound enzyme to induce a colored reaction product. The intensity of this colored product is directly proportional to the concentration of IL-10 present in the samples.


      This kit will recognize both endogenous and recombinant Human IL-10.


      Get results in 90 minutes with Human IL-10 ELISA Kit (ab185986) from our SimpleStep ELISA® range.


       


       


       

    • Platform

      Microplate

    Properties

    • Storage instructions

      Store at +4°C. Please refer to protocols.
    • Components Identifier 1 x 96 tests
      10X Standard Diluent Buffer Black 1 x 15ml
      200X Wash Buffer White 1 x 10ml
      Amplification Diluent Brown & blue spot 1 x 15ml
      Amplifier Yellow 1 x 200µl
      Biotinylated anti IL-10 Red 1 x 400µl
      Biotinylated Antibody Diluent Red 1 x 7.5ml
      Chromogen TMB Substrate Solution 1 x 11ml
      HRP Diluent Red 1 x 23ml
      IL-10 Microplate (12 x 8 well strips) 1 unit
      IL-10 Standard (Lyophilized) Yellow 2 vials
      Stop Reagent Black 1 x 11ml
      Streptavidin-HRP 2 x 5µl
    • Research areas

      • Immunology
      • Adaptive Immunity
      • T Cells
      • Non-CD
      • Immunology
      • Innate Immunity
      • Cytokines
      • Interleukins
      • Cancer
      • Tumor immunology
      • Cytokines
      • Interleukins
      • Immunology
      • Adaptive Immunity
      • Regulatory T Cells
      • Kits/ Lysates/ Other
      • Kits
      • ELISA Kits
      • ELISA Kits
      • Cytokines and cytokine receptors ELISA kits
      • Neuroscience
      • Processes
    • Function

      Inhibits the synthesis of a number of cytokines, including IFN-gamma, IL-2, IL-3, TNF and GM-CSF produced by activated macrophages and by helper T-cells.
    • Tissue specificity

      Produced by a variety of cell lines, including T-cells, macrophages, mast cells and other cell types.
    • Sequence similarities

      Belongs to the IL-10 family.
    • Cellular localization

      Secreted.
    • Target information above from: UniProt accession P22301 The UniProt Consortium
      The Universal Protein Resource (UniProt) in 2010
      Nucleic Acids Res. 38:D142-D148 (2010) .

      Information by UniProt
    • Alternative names

      • CSIF
      • Cytokine synthesis inhibitory factor
      • GVHDS
      • IL 10
      • IL-10
      • IL10
      • IL10_HUMAN
      • IL10A
      • Interleukin 10
      • Interleukin-10
      • MGC126450
      • MGC126451
      • T-cell growth inhibitory factor
      • TGIF
      see all
    • Database links

      • Entrez Gene: 3586 Human
      • Omim: 124092 Human
      • SwissProt: P22301 Human
      • Unigene: 193717 Human

      Associated products

      • SimpleStep ELISA kits

        • Human IL-10 ELISA Kit (Interleukin-10) (ab185986)

      Images

      • Typical Standard Curve
        Typical Standard Curve

        Representative Standard Curve using ab46059

      Protocols

      • Protocol Booklet

      Click here to view the general protocols

      Datasheets and documents

      • SDS download

      • Datasheet download

        Download

      References (5)

      Publishing research using ab46059? Please let us know so that we can cite the reference in this datasheet.

      ab46059 has been referenced in 5 publications.

      • Anier K  et al. Psychostimulant-induced aberrant DNA methylation in an in vitro model of human peripheral blood mononuclear cells. Clin Epigenetics 14:89 (2022). PubMed: 35842682
      • Sahbudak Bal Z  et al. Diagnostic Accuracy of Interleukin-6, Interleukin-8, and Interleukin-10 for Predicting Bacteremia in Children with Febrile Neutropenia. Turk J Haematol 34:254-257 (2017). PubMed: 28148470
      • Sammour I  et al. The Effect of Gender on Mesenchymal Stem Cell (MSC) Efficacy in Neonatal Hyperoxia-Induced Lung Injury. PLoS One 11:e0164269 (2016). PubMed: 27711256
      • Han K  et al. Efficacy of double-coated probiotics for irritable bowel syndrome: a randomized double-blind controlled trial. J Gastroenterol N/A:N/A (2016). PubMed: 27178566
      • Hasegawa T  et al. Chafuroside B, an Oolong Tea Polyphenol, Ameliorates UVB-Induced DNA Damage and Generation of Photo-immunosuppression Related Mediators in Human Keratinocytes. PLoS One 8:e77308 (2013). Sandwich ELISA ; Human . PubMed: 24116222

      Customer reviews and Q&As

      Show All Reviews Q&A
      Submit a question

      1-7 of 7 Q&A

      Question

      The ORDER #, which also was a replacement. We have been getting this high background in several different assay from Abcam, in addition, we are not seeing recovery of the spiked amounts in our samples. Do you have any suggestions as to why that is happening. We are autoclaving tips, water, tubes etc used before use. Sincerely,  

      Read More

      Abcam community

      Verified customer

      Asked on Mar 09 2012

      Answer

      Thank you for contacting us.

      I am sorry about the continued problems that you have been experiencing using this kit. Unfortunately I do not have any further suggestions to help with this issue. I have created a credit note/refund for the original purchase. Your credit note ID is 20001.

      I am sorry that this product did not perform as stated on the datasheet. I have asked our accounting department to issue a credit note for you, which can be redeemed against the invoice of a future order by passing it on to your purchasing department. To avoid confusion, please ensure your accounts department is aware of how the credit note is being used. If you have questions on how to use the credit note, please contact our accounting department.

      Our accounting department can be contacted by email at us.credits@abcam.com or by telephone using the information at the Contact Us link in the top right corner of our website. Please refer to the credit note ID in any correspondence with our accounting department.

      The credit note ID is for your reference only and does not automatically guarantee the credit.

      I hope this experience will not prevent you from purchasing other products from us in the future. Our Scientific Support team is always at your service, should you require further expert advice.

      Read More

      Abcam Scientific Support

      Answered on Mar 09 2012

      Question

      Thank you for passing this on.  We are eagerly and anxiously awaiting for your reply and perhaps some tips. The blank we use, is included in the standard curve as a "zero." Even though the absorbance is high.  We are concerned because our some of our unknown samples give less than the "zero" because the blank/zero is at a higher absorbance.  Furthermore, we are not seeing recovery of the spiked amounts in our samples.   Please let me know if there is any other information we can provide.  We appreciate your help and are looking forward to getting this working.

      Read More

      Abcam community

      Verified customer

      Asked on Feb 28 2012

      Answer

      I would like to suggest that you try using another kit to determine whether this is a product specific issue. If you provide me with the orginal Abcam order confirmation code I can send you a free of charge replacement for this product.



      Please let me know if you have any questions or there are other ways that Abcam may help you meet your research goals.

      Read More

      Abcam Scientific Support

      Answered on Feb 28 2012

      Question

      We have rerun some samples and standards using all the suggestions you provided on the phone and via email.  We ran only two test strips and the results still look odd. Attached is the data from those two strips.. I probably need to explain what each are. The spiked sample are way off. When I spiked a sample I mixed put 100ul sample with 90ul of a particular standard (all I had left of them) and the pipetted 100ul of this mixture to the plate just like the regular sample and standards.   We ran, a blank, low, mid and high standard twice (SA, SC, etc.) and (PA, PB, etc.) and these are highlighted in the excel sheet.  The others are either serum from control subjects or as indicated with the microliters, the subject samples spiked with standards, for which the results don't indicate the expected numbers.   As you can also see, the absorbance on the zero standard (the blanks) is high and the range of absorbances is small and low.  Can you please provide some help?  We appreciate any tips you can provide.  We have corresponded many times via phone and through email with you and are looking forward to getting some useful tips.

      Read More

      Abcam community

      Verified customer

      Asked on Feb 28 2012

      Answer

      I've passed this information on to the lab for you.

      They feel that the data enclosed are pretty good, except the blank which is indeed a little bit high, and which should rather be considered as a zero. They also also would like to confirm what you use as Blank/zero?

      Please let me know if you have any questions or there are other ways that Abcam may help you meet your research goals.

      Read More

      Abcam Scientific Support

      Answered on Feb 28 2012

      Question

      The standards were dissolved in the provided diluent. What is the matrix effect?  So despite the fact that we are getting low signal, do you suggestion diluting samples 1:2? I appreciate your help.  Thank you very much for your continued help on this kit.

      Read More

      Abcam community

      Verified customer

      Asked on Feb 06 2012

      Answer

      Thank you for that additional information. The matrix effect could be called quenching. The high protein concentration of serum samples or components contained in samples can affect assay response to the analyte (IL-10) and give background. If you dilute samples, then the matrix is altered and the recovery of analyte is better. The results obtained should be multiplied by the dilution factor.There is two different diluents provided in the kit, depending of what kind of samples are assaying (serum/plasmas or cell supernatents). We do recommend using these. I hope this information is helpful to you. Please do not hesitate to contact us should you have any questions.

      Read More

      Abcam Scientific Support

      Answered on Feb 06 2012

      Question

      We are running some cytokine ELISAs on human serum and plasma samples and have come across some trouble in our first run with your High Sensitivity IL10 Human ELISA kit ab46059.  I'm hoping you can help please.  For our first plate, we got very low signal in the curve andnothing in our samples. Could be because the curve didn’t really come out. Highest absorbance was 0.25.  We are wondering first, if you have any suggestions or any troubleshooting guides from perhaps previous customers with similar issues.  Our patient samples are from clinical samples that we expect to be in the range of the curve.  I've attached the data if that helps, and would also like to know if there is any possibility that you might provide another replacement kit before we begin to re-analyze our samples with your troubleshooting suggestions.  Are there any possible steps that quenching of signal can be an issue with human serum/plasma samples?  Are there other precautions we should be taking to avoid signal quenching?  We are most concerned because the standard curve gave such low signal as well.  If you have any suggestions, we are extremely grateful and appreciate your time, as we are on a very urgent schedule with this thesis project.

      Read More

      Abcam community

      Verified customer

      Asked on Feb 03 2012

      Answer

      Thank you for contacting Abcam.

      I have had the opportunity to speak with the lab regarding this issue. The low signal obtained may be linked to the use of human serum as standard curve diluent. Have you diluted the standards in human serum or in standard diluent buffer PBS/BSA? They also advise diluting the samples 1:2 to minimize the matrix effect.

      Please let me know if you have any questions.

      Read More

      Abcam Scientific Support

      Answered on Feb 03 2012

      Question

      Standard curve does not look normal and there is no signal with HIV+ human serum samples.

      Read More

      Abcam community

      Verified customer

      Asked on Jan 03 2012

      Answer

      Thank you for your call today, and for letting us know about the trouble with this kit. As we discussed, please forward any data you have using this kit, and I will see if there are any suggestions that we can make to improve the results. I look forward to hearing from you. Please let me know if you have any questions or if there is anything else that we can do for you.

      Read More

      Abcam Scientific Support

      Answered on Jan 03 2012

      Question

      What's the difference between these kits? In what situations would each be appropriate?

      Read More

      Abcam community

      Verified customer

      Asked on Oct 14 2011

      Answer

      Thank you for your call yesterday and for your patience while i have been in touch with the lab regarding these IL10 kits. Here is the reply that I received from my contact at the lab: "To be on the safe side regarding sensitivity, my opinion would be to use the High Sensitivity format, with dilution factor for plasmas 1:2 or 1:5. On the other hand, for someone new to ELISA, the Non-High Sensitivity one is easier to assay (less steps & more robust). According to general knowledge, IL-10 concentration is increased in HIV positive plasmas, so the detection level should be convenient." I hope this information will be useful in determining which of these kits will be most suitable for your studies, but please let me know if you have any further questions or if there is anything else that we can do for you.     v\:* {behavior:url(#default#VML);} o\:* {behavior:url(#default#VML);} w\:* {behavior:url(#default#VML);} .shape {behavior:url(#default#VML);}  

      Read More

      Abcam Scientific Support

      Answered on Oct 14 2011

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