Rabbit Recombinant Monoclonal CAPSD antibody. Carrier free. Suitable for WB, IHC-P, Flow Cyt (Intra), I-ELISA and reacts with Transfected cell lysate - Norovirus, Transfected cell line - Norovirus, Recombinant fragment - Norovirus samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
WB | IHC-P | Flow Cyt (Intra) | I-ELISA | ICC/IF | IP | |
---|---|---|---|---|---|---|
Norovirus | Predicted | Predicted | Predicted | Predicted | Not recommended | Not recommended |
Recombinant fragment - Norovirus | Not recommended | Not recommended | Not recommended | Tested | Not recommended | Not recommended |
Transfected cell line - Norovirus | Not recommended | Tested | Tested | Not recommended | Not recommended | Not recommended |
Transfected cell lysate - Norovirus | Tested | Not recommended | Not recommended | Not recommended | Not recommended | Not recommended |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell lysate - Norovirus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Norovirus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell line - Norovirus, Recombinant fragment - Norovirus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell line - Norovirus | Dilution info - | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Norovirus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell lysate - Norovirus, Recombinant fragment - Norovirus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell line - Norovirus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Norovirus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell lysate - Norovirus, Recombinant fragment - Norovirus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Recombinant fragment - Norovirus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Norovirus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell lysate - Norovirus, Transfected cell line - Norovirus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Norovirus, Transfected cell lysate - Norovirus, Transfected cell line - Norovirus, Recombinant fragment - Norovirus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Norovirus, Transfected cell lysate - Norovirus, Transfected cell line - Norovirus, Recombinant fragment - Norovirus | Dilution info - | Notes - |
VP1
Rabbit Recombinant Monoclonal CAPSD antibody. Carrier free. Suitable for WB, IHC-P, Flow Cyt (Intra), I-ELISA and reacts with Transfected cell lysate - Norovirus, Transfected cell line - Norovirus, Recombinant fragment - Norovirus samples.
pH: 7.2 - 7.4
Constituents: 100% PBS
The immunogen has been designed based on the Norovirus Hu/Texas/TCH04-577/2004/US and tested only with cells overexpressing Norovirus Capsid protein VP1
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
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 1 minute hands-on-time and 100% antibody recovery: available for fluorescent dyes, HRP, biotin and gold.
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.
The Norovirus Capsid protein VP1 also known as the Norwalk Capsid protein is a major structural component of noroviruses. The mass of this protein is approximately 58 kilodaltons. It is expressed within the viral particles forming the outer shell or capsid which plays an important role in protection and infectivity of the virus. VP1 is also the main target for capsid ELISA tests which are employed for virus detection.
Norovirus Capsid protein VP1 assembles into icosahedral particles forming the structure that encases the viral RNA. It works as part of a complex with other molecular groups to facilitate the virus’s entry into host cells by binding to histo-blood group antigens found on epithelial cells of the digestive tract. This protein’s structure allows it to adapt and evade the host immune response which plays role in the virus's infectivity.
Norovirus Capsid protein VP1 involves in pathways related to viral replication and immune evasion. Inside the host it participates in interactions that inhibit immune signaling pathways. These interactions often involve proteins like the Golgi-associated mechanics to promote efficient assembly and release of viral particles. VP1's interaction with cellular machinery ensures ongoing propagation of the virus.
The Norovirus Capsid protein VP1 directly connects to gastroenteritis a leading cause of acute viral gastroenteritis. It links to disease progression by aiding viral invasion and persistence in the gastrointestinal tract. The VP1's interactions with the immune system and histo-blood group antigens contribute to high transmissibility and variability of infection severity among different individuals.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
This data was developed using Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded rat pancreas tissue labeling Norovirus Capsid protein VP1 with Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068 at 1/5000 followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control: no staining on rat pancreas.
The section was incubated with Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
This data was developed using 308068, the same antibody clone in a different buffer formulation.
Blocking and diluting buffer and concentration: 5% NFDM/TBST
The band beneath the target band (62 kDa) is expected to be degradation products.
In Western blot, anti-His antibody (Anti-6X His tag® antibody [EPR20547] - ChIP Grade ab213204) staining at 1/5000 dilution.
In Western blot, anti-GAPDH antibody (Anti-GAPDH antibody [EPR16891] - Loading Control ab181602) loading control staining at 1/200000 dilution.
Exposure time: 3 seconds
All lanes: Western blot - Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] (Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068) at 1/1000 dilution
Lane 1: 293T whole cell lysate at 20 µg
Lane 2: 293T cells transfected with an empty vector containing a his tag whole cell lysate at 20 µg
Lane 3: 293T cells transfected with a Capsid protein VP1 expression vector containing a his tag whole cell lysate at 20 µg
All lanes: Western blot - Goat Anti-Rabbit IgG H&L (HRP) (Goat Anti-Rabbit IgG H&L (HRP) ab97051) at 1/100000 dilution
Observed band size: 62 kDa
Exposure time: 3s
This data was developed using Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded human pancreas tissue labeling Norovirus Capsid protein VP1 with Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068 at 1/5000 followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control: no staining on human pancreas (PMID:19266182).
The section was incubated with Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
This data was developed using Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded mouse pancreas tissue labeling Norovirus Capsid protein VP1 with Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068 at 1/5000 followed by ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Negative control: no staining on mouse pancreas.
The section was incubated with Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068 for 30 mins at room temperature. The immunostaining was performed on a Leica Biosystems BOND® RX instrument. Counterstained with Hematoxylin.
Heat mediated antigen retrieval was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
This data was developed using Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068, the same antibody clone in a different buffer formulation.
Immunohistochemical analysis of paraffin-embedded cells labeling Norovirus Capsid protein VP1 with Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068 at 1/5000 followed by a ready to use LeicaDS9800 (Bond™ Polymer Refine Detection).
Positive staining on (A) HEK-293T (human embryonic kidney epithelial cell) transfected with a Capsid protein VP1 expression vector containing a his tag, no staining on (B) HEK-293T transfected with empty vector containing a his tag.
The section was incubated with Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068 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 was performed with Tris-EDTA buffer (pH 9.0, Epitope Retrieval Solution2) for 20 mins.
This data was developed using Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068, the same antibody clone in a different buffer formulation.
Flow cytometric analysis of 4% paraformaldehyde fixed 90% methanol permeabilized HEK-293T cells (human embryonic kidney epithelial cells) transfected with Myc-tagged Capsid protein VP1 overexpression construct cells labelling Norovirus Capsid protein VP1 with Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068 at 1/5000 dilution (Right) compared with a Rabbit monoclonal IgG isotype control (Rabbit IgG, monoclonal [EPR25A] - Isotype Control ab172730) (Left) A Goat Anti-Rabbit IgG (Alexa Fluor® 488, Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081) at 1/5000 dilution was used as the secondary antibody. Cells were stained with rabbit IgG or Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068 and co-stained with anti-Myc tag conjugated to Alexa Fluor® 647.
This data was developed using Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068, the same antibody clone in a different buffer formulation.
Indirect ELISA analysis of Anti-Norovirus Capsid protein VP1 antibody [EPR27186-20] ab308068 at 0-1000 ng/ml.
The secondary antibody used was Alkaline Phosphatase-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L) at 1/2500 dilution.
Antigen: Capsid protein VP1
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