Anti-Thyroid Peroxidase/TPO antibody [EPR23574-405] - BSA and Azide free (ab278531)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR23574-405] to Thyroid Peroxidase/TPO - BSA and Azide free
- Suitable for: WB, IHC-P, IHC-Fr
- Reacts with: Mouse, Rat
Overview
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Product name
Anti-Thyroid Peroxidase/TPO antibody [EPR23574-405] - BSA and Azide free
See all Thyroid Peroxidase/TPO primary antibodies -
Description
Rabbit monoclonal [EPR23574-405] to Thyroid Peroxidase/TPO - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: WB, IHC-P, IHC-Frmore details
Unsuitable for: IP -
Species reactivity
Reacts with: Mouse, Rat -
Immunogen
Recombinant fragment. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- WB: Mouse and rat thyroid tissue lysate. IHC-P: Mouse and rat thyroid tissue. IHC-Fr: Mouse and rat thyroid tissue.
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General notes
Please Note: Clone [EPR23574-405] (this product) is different to that of ab275932 [EPR23574-130] for the same target.
ab278531 is the carrier-free version of ab278525.
Our carrier-free antibodies are typically supplied in a PBS-only formulation, purified and free of BSA, sodium azide and glycerol. The carrier-free buffer and high concentration allow for increased conjugation efficiency.
This conjugation-ready format is designed for use with fluorochromes, metal isotopes, oligonucleotides, and enzymes, which makes them ideal for antibody labelling, functional and cell-based assays, flow-based assays (e.g. mass cytometry) and Multiplex Imaging applications.
Use our conjugation kits for antibody conjugates that are ready-to-use in as little as 20 minutes with
This product is compatible with the Maxpar® Antibody Labeling Kit from Fluidigm, without the need for antibody preparation. Maxpar® is a trademark of Fluidigm Canada Inc.
This product is a recombinant monoclonal antibody, which offers several advantages including:
- - High batch-to-batch consistency and reproducibility
- - Improved sensitivity and specificity
- - Long-term security of supply
- - Animal-free production
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
Properties
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Form
Liquid -
Storage instructions
Shipped at 4°C. Store at +4°C. -
Storage buffer
Constituent: 100% PBS -
Carrier free
Yes -
Concentration information loading...
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Purity
Protein A purified -
Clonality
Monoclonal -
Clone number
EPR23574-405 -
Isotype
IgG -
Research areas
Images
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Anti-Thyroid Peroxidase/TPO antibody [EPR23574-405] (ab278525) at 1/1000 dilution + Mouse thyroid tissue lysate at 20 µg
Secondary
Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/100000 dilution (Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated)
Predicted band size: 103 kDa
Observed band size: 101 kDa why is the actual band size different from the predicted?This data was developed using ab278525, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
Exposure time: 3 minutes.
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This data was developed using ab278525, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse thyroid tissue labeling Thyroid Peroxidase/TPO with ab278525 at 1/5000 (0.109 µg/ml) followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection) was used. Cytoplasmic staining in mouse thyroid. The section was incubated with ab278525 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond® Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
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This data was developed using ab278525, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen mouse thyroid tissue labeling Thyroid Peroxidase/TPO with ab278525 at 1/500 (1.086 µg/ml) dilution followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Positive staining on mouse thyroid is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control: Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488)at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
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All lanes : Anti-Thyroid Peroxidase/TPO antibody [EPR23574-405] (ab278525) at 1/1000 dilution
Lane 1 : Rat thyroid tissue lysate
Lane 2 : Rat heart tissue lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG H&L (HRP) (ab97051) at 1/50000 dilution (Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated)
Predicted band size: 103 kDa
Observed band size: 101 kDa why is the actual band size different from the predicted?This data was developed using ab278525, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
TPO is expressed in thyroid. Positive signal is observed in thyroid tissue (PMID: 29541194), no signal is observed in heart tissue.
Exposure time: 3 minutes.
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This data was developed using ab278525, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat thyroid tissue labeling Thyroid Peroxidase/TPO with ab278525 at 1/5000 (0.109 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection) was used. Cytoplasmic staining in rat thyroid. The section was incubated with ab278525 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND®RX instrument. Counterstained with Hematoxylin.
Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond®Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.
-
This data was developed using ab278525, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen rat thyroid tissue labeling Thyroid Peroxidase/TPO with ab278525 at 1/500 (1.086 µg/ml) dilution followed by ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) at 1/1000 dilution (Green). Positive staining on rat thyroid is observed. The nuclear counterstain was DAPI (Blue).
Secondary antibody control: Secondary antibody is ab150077 Goat Anti-Rabbit IgG H&L (Alexa Fluor®488)at 1/1000 dilution.
Heat mediated antigen retrieval using sodium citrate buffer (10mM citrate pH 6.0 + 0.05% Tween-20).
-
This data was developed using ab278525, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat cardiac muscle tissue labeling Thyroid Peroxidase/TPO with ab278525 at 1/5000 (0.109 µg/ml) dilution followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection) was used. The section was incubated with ab278525 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
No staining in rat cardiac muscle.
Secondary antibody only control: Secondary antibody is a ready to use LeicaDS9800 (Bond® Polymer Refine Detection).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins.