Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87]
- BOND RX™ Validated
- 20ul selling size
- Recombinant
- RabMAb
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Rabbit Recombinant Monoclonal SHANK2 antibody. Suitable for WB, IHC-Fr, Flow Cyt (Intra), IHC-P and reacts with Recombinant fragment - Human, Human, Mouse, Rat samples.
View Alternative Names
CORTBP1, KIAA1022, PROSAP1, SH3 and multiple ankyrin repeat domains protein 2, Shank2, Cortactin-binding protein 1, Proline-rich synapse-associated protein 1, CortBP1
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized T-47D (human ductal breast epithelial tumor epithelial cell) (Right) / 293T (human embryonic kidney epithelial cell) (Left) cells labelling SHANK1 + SHANK2 + SHANK3 with ab317608 at 1/500 dilution (0.1ug)/Red (Red) compared with a Rabbit monoclonal IgG (ab172730) (Black) isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Low expression : 293T (PMID : 32661924)
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Immunohistochemical analysis of paraffin-embedded Mouse hippocampus tissue labeling SHANK1 + SHANK2 + SHANK3 with ab317608 at 1/100 (4.75 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Positive staining in mouse hippocampus (PMID : 27581745). The section was incubated with ab317608 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 Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Immunohistochemical analysis of paraffin-embedded Rat cerebellum tissue labeling SHANK1 + SHANK2 + SHANK3 with ab317608 at 1/100 (4.75 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Positive staining in rat cerebellum (PMID : 27581745). The section was incubated with ab317608 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 Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Immunohistochemical analysis of paraffin-embedded Mouse liver tissue labeling SHANK1 + SHANK2 + SHANK3 with ab317608 at 1/100 (4.75 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Positive staining on cholangiocytes in mouse liver (PMID : 14977424). The section was incubated with ab317608 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 Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Immunohistochemical analysis of paraffin-embedded Rat liver tissue labeling SHANK1 + SHANK2 + SHANK3 with ab317608 at 1/100 (4.75 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Positive staining on cholangiocytes in rat liver (PMID : 14977424). The section was incubated with ab317608 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 Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Mouse primary neuron cells labelling SHANK1 + SHANK2 + SHANK3 with ab317608 at 1/500 dilution (0.1ug)/right (Red) compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Immunohistochemical analysis of paraffin-embedded Rat skeletal muscle tissue labeling SHANK1 + SHANK2 + SHANK3 with ab317608 at 1/100 (4.75 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Negative control : No staining on rat skeletal muscle (PMID : 10506216). The section was incubated with ab317608 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 Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC-P
Supplier Data
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Immunohistochemical analysis of paraffin-embedded Mouse skeletal muscle tissue labeling SHANK1 + SHANK2 + SHANK3 with ab317608 at 1/100 (4.75 ug/ml) dilution, followed by a ready to use Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Negative control : No staining on mouse skeletal muscle (PMID : 10506216). The section was incubated with ab317608 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 Rabbit specific IHC polymer detection kit HRP/DAB (ab209101).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 20 mins
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse skeletal muscle (fresh frozen) tissue labeling SHANK1 + SHANK2 + SHANK3 with ab317608 at 1/100 (4.75 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green).
Negative control : confocal image showing no staining on mouse skeletal muscle. The nuclear counterstain was DAPI (Blue). The section was incubated with ab317608 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
- Flow Cyt (Intra)
Supplier Data
Flow Cytometry (Intracellular) - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized Mouse spleen cell cells labelling SHANK1 + SHANK2 + SHANK3 with ab317608 at 1/500 dilution (0.1ug)/right (Red) compared with a Rabbit monoclonal IgG (ab172730) / Left isotype control and an unlabelled control (cells without incubation with primary antibody and secondary antibody) (Blue).
Goat Anti-Rabbit IgG (Alexa Fluor® 488, ab150081) at 1/5000 dilution was used as the secondary antibody.
Negative control : mouse spleen cell.
- IHC-Fr
Supplier Data
Immunohistochemistry (Frozen sections) - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Immunohistochemical analysis of 4% PFA-fixed, 0.2% Triton X-100 permeabilized frozen Mouse hippocampus (fresh frozen) tissue labeling SHANK1 + SHANK2 + SHANK3 with ab317608 at 1/100 (4.75 ug/ml) dilution followed by ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/1000 2 ug/mL dilution (Green).
Confocal image showing positive staining on mouse hippocampus. The nuclear counterstain was DAPI (Blue). The section was incubated with ab317608 for 60 mins at room temperature. The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Secondary antibody control : Secondary antibody is ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbedat 1/1000 2 ug/mL dilution.
- WB
Supplier Data
Western blot - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
This antibody can recognize human SHANK1, SHANK2 and SHANK3. .
In Western blot, Anti-6X His tag® antibody [EPR20547] - ChIP Grade (ab213204) staining at 1/5000 dilution.
All lanes:
Western blot - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (ab317608) at 1/1000 dilution
Lane 1:
His-tagged human SHANK2 recombinant fragment at 10 ng
Lane 2:
His-tagged human SHANK1 recombinant fragment at 10 ng
Lane 3:
His-tagged human SHANK3 recombinant fragment at 10 ng
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/100000 dilution
Observed band size: 26 kDa
false
Exposure time: 125s
- WB
Supplier Data
Western blot - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Negative control : skeletal muscle (PMID : 10506216; PMID : 22346768).
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 10506216). The bands beneath the target band (180-240 kDa) are likely to be degraded target fragments.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.
All lanes:
Western blot - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (ab317608) at 1/1000 dilution
Lane 1:
Human hippocampus tissue lysate at 20 µg
Lane 2:
Human skeletal muscle tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/200000 dilution
Observed band size: 180-240 kDa,124 kDa
false
Exposure time: 180s
- WB
Supplier Data
Western blot - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Low expression : 293T (PMID : 32661924).
The molecular weight observed is consistent with what has been described in the literature (PMID : 10506216). The bands beneath the target band (180-270 kDa) are likely to be degraded target fragments.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.
All lanes:
Western blot - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (ab317608) at 1/1000 dilution
Lane 1:
T-47D (human ductal breast epithelial tumor epithelial cell) whole cell lysate at 20 µg
Lane 2:
293T (human embryonic kidney epithelial cell) whole cell lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 180-270 kDa,124 kDa
false
Exposure time: 15s
- WB
Supplier Data
Western blot - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (AB317608)
Negative control : skeletal muscle (PMID : 10506216; PMID : 22346768).
The expression profile/ molecular weight observed is consistent with what has been described in the literature (PMID : 10506216). The bands beneath the target band (180-270 kDa) are likely to be degraded target fragments.
In Western blot, Anti-Vinculin antibody [EPR8185] (ab129002) staining at 1/10000 dilution.
All lanes:
Western blot - Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] (ab317608) at 1/1000 dilution
Lane 1:
Mouse cerebellum tissue lysate at 20 µg
Lane 2:
Mouse hippocampus tissue lysate at 20 µg
Lane 3:
Mouse skeletal muscle tissue lysate at 20 µg
Lane 4:
Rat cerebellum tissue lysate at 20 µg
Lane 5:
Rat hippocampus tissue lysate at 20 µg
Lane 6:
Rat skeletal muscle tissue lysate at 20 µg
Secondary
All lanes:
Western blot - Goat Anti-Rabbit IgG H&L (HRP) (<a href='/en-us/products/secondary-antibodies/goat-rabbit-igg-h-l-hrp-ab97051'>ab97051</a>) at 1/20000 dilution
Observed band size: 180-270 kDa,124 kDa
false
Exposure time: 59s
Related conjugates and formulations (1)
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Anti-SHANK1 + SHANK2 + SHANK3 antibody [EPR26549-87] - BSA and Azide free
Reactivity data
Product details
Patented technology
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
What are the advantages of a recombinant monoclonal antibody?
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 batch production
For more information, read more on recombinant antibodies.
Properties and storage information
Form
Purification technique
Storage buffer
Shipped at conditions
Appropriate short-term storage duration
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
SHANK proteins are integral to the formation and function of synaptic assemblies. They are components of a complex called the postsynaptic density where they link neurotransmitter receptors with cytoskeletal elements. These proteins play an important role in organizing the synaptic machinery necessary for neurotransmission. By anchoring various receptors and proteins at synapses SHANK proteins influence synaptic strength and plasticity essential for learning and memory.
Pathways
SHANK proteins are critical in the N-methyl-D-aspartate receptor (NMDAR) and metabotropic glutamate receptor (mGluR) signaling pathways. SHANK proteins associate with proteins like Homer and GKAP which modulate these pathways. By interacting with these partners SHANK proteins contribute to the regulation of excitatory synaptic transmission and are involved in mechanisms of synaptic plasticity such as long-term potentiation.
Product protocols
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Target data
Additional targets
Product promise
Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.
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