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Goat Anti-Mouse IgG H&L (TRITC) (ab6786)

Submit a review Q&A (2)References (47)
Flow Cytometry - Goat Anti-Mouse IgG H&L (TRITC) (ab6786)

    Key features and details

    • Goat Anti-Mouse IgG H&L (TRITC)
    • Conjugation: TRITC. Ex: 547nm, Em: 572nm
    • Host species: Goat
    • Isotype: IgG
    • Suitable for: Immunomicroscopy, Flow Cyt, IHC-P, IHC-Fr, ICC/IF, ELISA

    Conjugates logo Related conjugates and formulations

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    Overview

    • Product name

      Goat Anti-Mouse IgG H&L (TRITC)
      See all IgG secondary antibodies

    • Host species

      Goat

    • Target species

      Mouse

    • Tested applications

      Suitable for: Immunomicroscopy, Flow Cyt, IHC-P, IHC-Fr, ICC/IF, ELISAmore details

    • Immunogen

      Mouse IgG whole molecule

    • Conjugation

      TRITC. Ex: 547nm, Em: 572nm

    Properties

    • Form

      Liquid

    • Storage instructions

      Shipped at 4°C. Store at +4°C short term (1-2 weeks). Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.

    • Storage buffer

      Preservative: 0.01% Sodium azide
      Constituents: 0.878% Sodium chloride, 1% BSA, 0.424% Potassium phosphate
    • Concentration information loading...

    • Purity

      Affinity purified

    • Purification notes

      This product was prepared from monospecific antiserum by immunoaffinity chromatography using mouse IgG coupled to agarose beads followed by solid phase adsorption(s) to remove any unwanted reactivities.

    • Conjugation notes

      Tetramethylrhodamine isothiocyanate (TRITC) (Molecular Weight 444 daltons) Absorption Wavelength: 550 nm Emission Wavelength: 570 nm Fluorochrome/Protein Ratio: 2.8 moles TRITC per mole of Rabbit IgG

    • Clonality

      Polyclonal

    • Isotype

      IgG

    • Research areas

    Applications

    The Abpromise guarantee

    Our Abpromise guarantee covers the use of ab6786 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
    Immunomicroscopy
    Use at an assay dependent concentration.
    Flow Cyt
    1/2000 - 1/4000.
    IHC-P
    Use at an assay dependent concentration.
    IHC-Fr
    Use at an assay dependent concentration.
    ICC/IF
    1/1000 - 1/5000. (PubMed:15659422)
    ELISA
    1/10000 - 1/50000.
    Notes
    Immunomicroscopy
    Use at an assay dependent concentration.
    Flow Cyt
    1/2000 - 1/4000.
    IHC-P
    Use at an assay dependent concentration.
    IHC-Fr
    Use at an assay dependent concentration.
    ICC/IF
    1/1000 - 1/5000. (PubMed:15659422)
    ELISA
    1/10000 - 1/50000.

    Images

    • Flow Cytometry - Goat Anti-Mouse IgG H&L (TRITC) (ab6786)
      Flow Cytometry - Goat Anti-Mouse IgG H&L (TRITC) (ab6786)
      Overlay histogram showing Jurkat cells stained with ab8090 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab8090, 0.1μg/1x106 cells) for 30 min at 22°C. The secondary antibody Goat anti-mouse IgG H&L (TRITC) (ab6786) was used at 1/4000 dilution for 30 min at 22°C. Isotype control antibody (black line) was mouse IgG2a [ICIGG2A] (ab91361, 0.1μg/1x106 cells) used under the same conditions. Unlabelled sample (blue line) was also used as a control. Acquisition of >5,000 events were collected using a 561nm laser and 610/20 bandpass filter.

    Protocols

    To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.

    Click here to view the general protocols

    References (47)

    Publishing research using ab6786? Please let us know so that we can cite the reference in this datasheet.

    ab6786 has been referenced in 47 publications.

    • Qi X  et al. Shp2 suppresses fat accumulation in white adipose tissue by activating Wnt/ß-catenin signaling following vertical sleeve gastrectomy in obese rats with type-2 diabetes. Exp Ther Med 23:302 (2022). PubMed: 35340882
    • Lee G  et al. Broad-Spectrum Antiviral Activity of 3D8, a Nucleic Acid-Hydrolyzing Single-Chain Variable Fragment (scFv), Targeting SARS-CoV-2 and Multiple Coronaviruses In Vitro. Viruses 13:N/A (2021). PubMed: 33918914
    • Zhao R  et al. Production of viable chicken by allogeneic transplantation of primordial germ cells induced from somatic cells. Nat Commun 12:2989 (2021). PubMed: 34017000
    • Zhang C  et al. H3K4me2 Promotes the Activation of lncCPSET1 by Jun in the Chicken PGC Formation. Animals (Basel) 11:N/A (2021). PubMed: 34072197
    • Palomba R  et al. Boosting nanomedicine performance by conditioning macrophages with methyl palmitate nanoparticles. Mater Horiz 8:2726-2741 (2021). PubMed: 34617542
    View all Publications for this product

    Customer reviews and Q&As

    Show All Reviews Q&A
    Submit a review Submit a question

    1-2 of 2 Abreviews or Q&A

    Question

    I bought the primary antibody (Primary antibody (mouse anti CK3): https://www.abcam.com/Cytokeratin-3-antibody-AE5-ab77869.html) and secondary antibody (goat anti-mouse 1)https://www.abcam.com/Goat-polyclonal-Secondary-Antibody-to-Mouse-IgG-H-L-FITC-pre-adsorbed-ab97039.html
    2) https://www.abcam.com/Mouse-IgG-secondary-antibody-H-L-ab6786.html) from you.

    And I used rabbit cornea as the control and I tried several times for the positive control and negative control. But the results were weird.










    All the slides which stained with FITC were positive (for negative control also showed positive staining)

    All the slides which stained with TRITC were negative (for positive control also showed negative staining)



    And I attach the immunostaining fotos and the protocol what I used for the immunostaing in the attachment. Could you please help me check if the antibodies what I chosen are not proper or the protocol what I used is not proper?? If it is, please send me a proper protocol for the immunostaining ! Thank you very much for your help!

    Read More
    Answer

    Thank you for contacting Abcam.

    I will be happy to help you further in this matter, but I just have a few more questions for you:

    1 - Were you staining tissue sections or a monolayer of cultured cells?

    2 - If you were staining sections, how were they prepared (PfA fixation & paraffin embedded, MeOH etc)?

    3 - If these samples were paraffin embedded, what type of antigen retrieval did you use on them?

    4 - Have you used either of the secondary antibodies successfully with other primary antibodies?

    I look forward to your reply and helping to resolve these issues.

    Read More

    Question

    I would just like to know if your secondary antibody ab6786 (goat polyclonal to mouse IgG H&L conjugated to Rhodamine) would be suitable in conjunction with antibody ab8329 (EBNA 1 antibody, mouse monoclonal IgG2b). It is not listed in your list of recommended secondaries for this antibody, but I cannot see from the data sheet why it would not work, Please advise,

    Read More
    Answer

    Thank you for your enquiry. Yes, ab6786 - Goat polyclonal to Mouse IgG H&L (rhodamine) - would be a suitable secondary antibody to use with ab8329 - Mouse monoclonal [E1-2.5] to EBNA 1. The list of compatible secondaries located at the bottom of the datasheets are just suggestions, and don't encompass all of the secondary antibodies that we have that can be used with that particular primary antibody. If you have any additional questions, please let us know.

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