Rabbit Monoclonal Enterovirus D68 VP1 antibody antibody. Carrier free. Suitable for sELISA, WB and reacts with Recombinant full length protein - Enterovirus D68, Enterovirus D68, Transfected cell lysate - Enterovirus D68 samples.
pH: 7.4
Constituents: 100% PBS
sELISA | WB | |
---|---|---|
Enterovirus D68 | Expected | Tested |
Recombinant full length protein - Enterovirus D68 | Tested | Not recommended |
Transfected cell lysate - Enterovirus D68 | Not recommended | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Recombinant full length protein - Enterovirus D68 | Dilution info - | Notes Please notice that ab308217 needs to be conjugated to HRP to function as the detection antibody when paired with Anti-Enterovirus D68 VP1 antibody [GT1843] - BSA and Azide free ab308408. |
Species | Dilution info | Notes |
---|---|---|
Species Enterovirus D68 | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell lysate - Enterovirus D68 | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Enterovirus D68 | Dilution info 1/1000 | Notes - |
Species Transfected cell lysate - Enterovirus D68 | Dilution info 1/1000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Recombinant full length protein - Enterovirus D68 | Dilution info - | Notes - |
Rabbit Monoclonal Enterovirus D68 VP1 antibody antibody. Carrier free. Suitable for sELISA, WB and reacts with Recombinant full length protein - Enterovirus D68, Enterovirus D68, Transfected cell lysate - Enterovirus D68 samples.
pH: 7.4
Constituents: 100% PBS
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.
Enterovirus VP1 also known as viral protein 1 is a structural protein of the enterovirus capsid. It has a mass of approximately 30 kilodaltons and plays an important role in virus assembly and host cell interaction. The protein is expressed on the viral surface and it is responsible for initial binding to the host cell receptors. This interaction facilitates the entry of the virus into cells initiating the infectious cycle. Enterovirus VP1 is highly conserved among different enterovirus serotypes which allows it to serve as a target for diagnostics and therapeutic interventions.
This protein enables the structural integrity and infectivity of the virus. Enterovirus VP1 is a part of the viral capsid a protein complex that also includes VP2 VP3 and VP4. These proteins collectively protect the viral RNA genome and are involved in mediating interactions with the host immune system. The conformational structure of VP1 is recognized by neutralizing antibodies making it a focus point for vaccine development and antiviral drugs. Its expression and conformation can influence the antigenicity and serotype specificity of enteroviruses.
Several actions revolving around host-pathogen interactions involve Enterovirus VP1. It plays a pivotal role in the cell entry mechanism through endocytic pathways. VP1 interacts with proteins such as ICAM-1 or PSGL-1 which serves as receptors in the early stages of viral pathogenesis. Additionally during viral uncoating and RNA release VP1 undergoes structural rearrangements that are essential for subsequent steps in the viral lifecycle and involve complex pathways like the host cell defense mechanism.
Alterations in Enterovirus VP1 are significant in the context of ailments like hand foot and mouth disease and viral myocarditis. The protein's sequence variations can influence disease severity and transmission. Furthermore correlations have been established between the structural aspects of VP1 and host proteins involved in disease manifestation such as cellular kinases influencing viral replication. This protein's interactions and mutations contribute to the pathogenicity and epidemiology of enterovirus-related diseases.
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.
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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.
Sandwich ELISA detection of recombinant full-length VP1 protein(s) derived from different strains of Enterovirus (D68; 71) using antibodies as below:
Capture: Anti-Enterovirus D68 VP1 antibody [GT1843] - BSA and Azide free ab308408 (5 μg/mL)
Detection: ab308217 (1 μg/mL)
Non-infected (–) and infected (+) RD whole cell extracts (20 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with Enterovirus D68 VP1 antibody [HL1997] (ab308217) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Lane 1: Non-infected RD whole cell extracts at 20 µg
Lane 2: Enterovirus 71 C2 infected RD whole cell extracts at 20 µg
Lane 3: Enterovirus D68 infected RD whole cell extracts at 20 µg
Lane 4: Coxsackievirus A6 infected RD whole cell extracts at 20 µg
All lanes: HRP-conjugated anti-rabbit IgG antibody
Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with Enterovirus D68 VP1 antibody [HL1997] (ab308217) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Lane 1: Non-transfected 293T cell extracts at 30 µg
Lane 2: DDDDK- tagged enterovirus D68 VP1 transfected 293T whole cell extracts at 30 µg
Lane 3: DDDDK- tagged enterovirus 71 VP1 transfected 293T whole cell extracts at 30 µg
All lanes: HRP-conjugated anti-rabbit IgG antibody
Non-infected (–) and infected (+) RD whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with Enterovirus D68 VP1 antibody [HL1997] (ab308217) diluted at 1:1000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
Lane 1: Non-infected RD whole cell extracts at 30 µg
Lane 2: Infected RD whole cell extracts at 30 µg
All lanes: HRP-conjugated anti-rabbit IgG antibody
Sandwich ELISA detection of recombinant full-length VP1 protein(s) derived from different strains of Enterovirus (D68; 71) using ab308217 as detection antibody (1 μg/mL).
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