Rabbit Recombinant Monoclonal POLN antibody. Carrier free. Suitable for ICC/IF, IHC-P, WB and reacts with Transfected cell line - Venezuelan equine encephalitis virus samples. Immunogen corresponding to Recombinant Fragment Protein within Venezuelan equine encephalitis virus (strain P676) Polyprotein 1234.
pH: 7.4
Constituents: 100% PBS
ICC/IF | IHC-P | WB | |
---|---|---|---|
Transfected cell line - Venezuelan equine encephalitis virus | Tested | Tested | Tested |
Venezuelan equine encephalitis virus | Predicted | Predicted | Predicted |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell line - Venezuelan equine encephalitis virus | Dilution info 1/500 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Venezuelan equine encephalitis virus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell line - Venezuelan equine encephalitis virus | Dilution info 1/1000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Venezuelan equine encephalitis virus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell line - Venezuelan equine encephalitis virus | Dilution info 1/1000 - 1/10000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Venezuelan equine encephalitis virus | Dilution info - | Notes - |
Polyprotein P1234. Inactive precursor of the viral replicase, which is activated by cleavages carried out by the viral protease nsP2. Polyprotein P123. The early replication complex formed by the polyprotein P123 and nsP4 synthesizes the minus-strand RNAs (antigenome) (By similarity). Polyprotein P123 is a short-lived polyprotein that accumulates during early stage of infection (Probable). As soon P123 is cleaved into mature proteins, the plus-strand RNAs synthesis begins (By similarity). Polyprotein P123'. The early replication complex formed by the polyprotein P123' and nsP4 synthesizes minus-strand RNAs (antigenome) (Probable). Polyprotein P123' is a short-lived polyprotein that accumulates during early stage of infection (Probable). As soon P123' is cleaved into mature proteins, the plus-strand RNAs synthesis begins (Probable). mRNA-capping enzyme nsP1. Cytoplasmic capping enzyme that catalyzes two virus-specific reactions: methyltransferase and nsP1 guanylyltransferase (PubMed:26041283). mRNA-capping is necessary since all viral RNAs are synthesized in the cytoplasm, and host capping enzymes are restricted to the nucleus (Probable). The enzymatic reaction involves a covalent link between 7-methyl-GMP and nsP1, whereas eukaryotic capping enzymes form a covalent complex only with GMP (Probable). NsP1 capping consists in the following reactions: GTP is first methylated into 7-methyl-GMP and then is covalently linked to nsP1 to form the m7GMp-nsP1 complex from which 7-methyl-GMP complex is transferred to the mRNA to create the cap structure (PubMed:26041283). NsP1 is also needed for the initiation of the minus-strand RNAs synthesis (By similarity). Probably serves as a membrane anchor for the replication complex composed of nsP1-nsP4 (By similarity). Nsp1 is needed for the initiation of the minus-strand RNAs synthesis (By similarity). Palmitoylated nsP1 is remodeling host cell cytoskeleton, and induces filopodium-like structure formation at the surface of the host cell (By similarity). Protease nsP2. Multifunctional protein whose N-terminus is part of the RNA polymerase complex and displays NTPase, RNA triphosphatase and helicase activities (By similarity). NTPase and RNA triphosphatase are involved in viral RNA capping and helicase keeps a check on the dsRNA replication intermediates (By similarity). The C-terminus harbors a protease that specifically cleaves the polyproteins and releases the mature proteins (By similarity). Required for the shutoff of minus-strand RNAs synthesis (By similarity). Inhibits host translation to ensure maximal viral gene expression and evade host immune response (By similarity). Non-structural protein 3. Seems to be essential for minus-strand RNAs and subgenomic 26S mRNAs synthesis (By similarity). Displays mono-ADP-ribosylhydrolase activity (By similarity). ADP-ribosylation is a post-translational modification that controls various processes of the host cell and the virus probably needs to revert it for optimal viral replication (By similarity). Binds proteins of FXR family and sequesters them into the viral RNA replication complexes thereby inhibiting the formation of host stress granules on viral mRNAs (By similarity). The nsp3-FXR complexes bind viral RNAs and probably orchestrate the assembly of viral replication complexes, thanks to the ability of FXR family members to self-assemble and bind DNA (By similarity). Non-structural protein 3'. Seems to be essential for minus-strand RNAs and subgenomic 26S mRNAs synthesis (By similarity). Displays mono-ADP-ribosylhydrolase activity (Probable). ADP-ribosylation is a post-translational modification that controls various processes of the host cell and the virus probably needs to revert it for optimal viral replication (Probable). Binds proteins of FXR family and sequesters them into the viral RNA replication complexes thereby inhibiting the formation of host stress granules on viral mRNAs (Probable). The nsp3'-FXR complexes bind viral RNAs and probably orchestrate the assembly of viral replication complexes, thanks to the ability of FXR family members to self-assemble and bind DNA (Probable). RNA-directed RNA polymerase nsP4. RNA dependent RNA polymerase (By similarity). Replicates genomic and antigenomic RNA by recognizing replications specific signals. The early replication complex formed by the polyprotein P123 and nsP4 synthesizes minus-strand RNAs (By similarity). The late replication complex composed of fully processed nsP1-nsP4 is responsible for the production of genomic and subgenomic plus-strand RNAs (By similarity).
Polyprotein P1234, P1234, Non-structural polyprotein
Rabbit Recombinant Monoclonal POLN antibody. Carrier free. Suitable for ICC/IF, IHC-P, WB and reacts with Transfected cell line - Venezuelan equine encephalitis virus samples. Immunogen corresponding to Recombinant Fragment Protein within Venezuelan equine encephalitis virus (strain P676) Polyprotein 1234.
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.
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Immunofluorescent analysis of Venezuelan equine encephalitis virus infected cells using ab313935 at a 1/100 dilution (Green). The nuclear counterstain is DAPI (Blue).
Samples were seperated by 10% SDS-PAGE.
All lanes: Western blot - Anti-Venezuelan equine encephalitis virus nsp3 antibody [HL1502] - BSA and Azide free (ab313935) at 1/5000 dilution
Lane 1: Non-transfected (–) 293T whole cell extracts
Lane 2: Transfected (+) 293T whole cell extracts
All lanes: HRP-conjugated anti-rabbit IgG antibody
Predicted band size: 277 kDa
Immunohistochemical analysis of paraffin-embedded mock and Venezuelan equine encephalitis virus (VEEV) nsp3 transfected HEK-293T (Human epithelial cell line from embryonic kidney transformed with large T antigen) cell pellets labeling Venezuelan equine encephalitis virus nsp3 with ab313935 at 1/1000 dilution. Blue: Fluoroshield with DAPI. Antigen retrieval performed using citrate buffer, pH 6.0 for 15 minutes.
Immunofluorescent analysis of mock and Venezuelan equine encephalitis virus nsp3 transfected HEK-293T (Human epithelial cell line from embryonic kidney transformed with large T antigen) cells fixed in 4% paraformaldehyde at room temperature for 15 minutes labelling Venezuelan equine encephalitis virus nsp3 with ab313935 at 1/500 dilution (green). Blue: Fluoroshield with DAPI.
All lanes: Western blot - Anti-Venezuelan equine encephalitis virus nsp3 antibody [HL1502] - BSA and Azide free (ab313935) at 1/5000 dilution
Lane 1: Untransfected HEK-293T (Human epithelial cell line from embryonic kidney transformed with large T antigen) whole cell extract at 30 µg
Lane 2: Venezuelan equine encephalitis virus nsp3 transfected HEK293T whole cell extract at 30 µg
All lanes: HRP-conjugated anti-rabbit IgG antibody
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