Anti-SHANK2 antibody [EPR24142-35] - BSA and Azide free (ab277532)
Key features and details
- Produced recombinantly (animal-free) for high batch-to-batch consistency and long term security of supply
- Rabbit monoclonal [EPR24142-35] to SHANK2 - BSA and Azide free
- Suitable for: IHC-P, WB
- Reacts with: Mouse, Rat
Overview
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Product name
Anti-SHANK2 antibody [EPR24142-35] - BSA and Azide free
See all SHANK2 primary antibodies -
Description
Rabbit monoclonal [EPR24142-35] to SHANK2 - BSA and Azide free -
Host species
Rabbit -
Tested applications
Suitable for: IHC-P, WBmore details
Unsuitable for: Flow Cyt,ICC/IF,IHC-Fr or IP -
Species reactivity
Reacts with: Mouse, Rat -
Immunogen
Synthetic peptide. This information is proprietary to Abcam and/or its suppliers.
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Positive control
- WB: Mouse hippocampus tissue lysate; rat brain and hippocampus tissue lysates. IHC-P: Mouse cerebrum and hippocampus tissue; Rat liver and hippocampus tissue.
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General notes
ab277532 is the carrier-free version of ab259966.
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
EPR24142-35 -
Isotype
IgG -
Research areas
Images
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All lanes : Anti-SHANK2 antibody [EPR24142-35] (ab259966) at 1/1000 dilution
Lane 1 : Mouse hippocampus tissue lysate
Lane 2 : Rat brain tissue lysate
Lane 3 : Rat hippocampus tissue lysate
Lysates/proteins at 20 µg per lane.
Secondary
All lanes : Goat Anti-Rabbit IgG, (H+L), Peroxidase conjugated (ab97051) at 1/100000 dilution
Predicted band size: 159 kDa
Observed band size: 165 kDa why is the actual band size different from the predicted?This data was developed using ab259966, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST.
Shank2 is expressed predominately in brain tissue what has described in the literature. (PMID: 9742101).
Exposure time: 3 minutes.
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This data was developed using ab259966, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse cerebrum tissue labeling SHANK2 with ab259966 at 1/5000 (0.0924 µg/ml) followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Cytoplasmic stainig on mouse cerebrum (PMID:29572432, 28179641). The section was incubated with ab259966 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 ab259966, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse hippocampus tissue labeling SHANK2 with ab259966 at 1/5000 (0.0924 µg/m) followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Cytoplasmic stainig on mouse hippocampus (PMID: 27581745, 29572432, 28179641). The section was incubated with ab259966 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 ab259966, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat liver tissue labeling SHANK2 with ab259966 at 1/5000 (0.0924 µg/ml) followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Positive staining on bile duct in rat liver (PMID: 14977424). The section was incubated with ab259966 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 ab259966, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat hippocampus tissue labeling SHANK2 with ab259966 at 1/5000 (0.0924 µg/ml) followed by a ready to use LeicaDS9800 (Bond® Polymer Refine Detection). Cytoplasmic stainig on rat hippocampus. The section was incubated with ab259966 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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