Rabbit Monoclonal Zika virus NS4B protein antibody. Carrier free. Suitable for ICC/IF, WB, IHC-P and reacts with Zika virus, Transfected cell line - Zika virus samples.
pH: 7.4
Constituents: 100% PBS
ICC/IF | WB | IHC-P | |
---|---|---|---|
Transfected cell line - Zika virus | Not recommended | Tested | Tested |
Zika virus | Tested | Tested | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Zika virus | Dilution info 1/100 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell line - Zika virus | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell line - Zika virus | Dilution info 1/1000.00000 - 1/5000.00000 | Notes - |
Species Zika virus | Dilution info 1/1000.00000 - 1/5000.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell line - Zika 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 Zika virus | Dilution info Use at an assay dependent concentration. | Notes - |
Rabbit Monoclonal Zika virus NS4B protein antibody. Carrier free. Suitable for ICC/IF, WB, IHC-P and reacts with Zika virus, Transfected cell line - Zika virus 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.
The Zika virus envelope protein also known as the E protein facilitates the virus's entry into host cells. This protein participates in the virus's attachment and fusion processes. It generally consists of three domains and has an approximate molecular mass of 53 kDa. Expression of this envelope protein occurs on the surface of the Zika virus particle after its synthesis in the host cell's endoplasmic reticulum. E proteins allow the Zika virus to interact with cell receptors aiding in the virus's ability to establish an infection.
The Zika virus envelope protein initiates fusion with the host cell membrane enabling the release of viral RNA into the host cytoplasm. This process is not solitary; it works as part of a complex involving other viral proteins like the membrane protein (M protein). The E protein has a role in immune system evasion by altering its structure and glycan shielding which complicates recognition by host antibodies. These aspects help the virus persist and replicate within its host.
The Zika virus envelope protein engages in the viral entry and replication pathways. A critical pathway involves receptor-mediated endocytosis reliant on host cell receptors to internalize the virus. The E protein works alongside the prM protein a precursor of the M protein to facilitate structural rearrangement necessary for the membrane fusion. The protein also impacts signaling pathways that influence the host's cell cycle which provides a favorable environment for viral replication and expression.
Several are associated with the activity of the Zika virus envelope protein. It is most notably linked to Zika virus infections which can lead to microcephaly and other severe birth defects in newborns when contracted during pregnancy. The envelope protein interacts with host immune proteins like the complement system which sometimes leads to an exaggerated immune response complicating recovery and potentially causing autoimmunity. Zika's E protein shares similarities with envelope proteins of other flaviviruses such as Dengue virus which further complicates immune recognition due to cross-reactive antibodies.
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.
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Immunohistochemical analysis of paraffin-embedded mock and Zika virus NS4B transfected HEK293T labeling Zika virus NS4B protein with ab308183 at 1/1000 dilution. Heat mediated antigen retrieval was performed with citrate buffer pH 6.0 for 15 mins.
For immunofluorescence analysis, Zika virus non-infected (left) and infected cells (right) were fixed and permeabilized for detection of Zika virus NS4B protein using ab308183 at 1/100 dilution (green). Nuclei (blue) is stained with fluoroshield with DAPI.
Non-infected (–) and infected (+) C6/36 whole cell extracts (5 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with Zika virus NS4B protein antibody [HL1663] (ab308183) diluted at 1/1000. A HRP-conjugated anti-rabbit IgG antibody (GTX213110-01) was used to detect the primary antibody.
All lanes: Western blot - Anti-Zika virus NS4B protein antibody [HL1663] (ab308183) at 1/1000 dilution
Lane 1: Non-infected (–) C6/36 whole cell lysate at 5 µg
Lane 2: Infected (+) C6/36 whole cell lysate at 5 µg
All lanes: HRP-conjugated anti-rabbit IgG antibody
Predicted band size: 27 kDa
Non-transfected (–) and transfected (+) 293T whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with Zika virus NS4B protein antibody [HL1663] (ab308183) diluted at 1/5000. A HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes: Western blot - Anti-Zika virus NS4B protein antibody [HL1663] (ab308183) at 1/5000 dilution
Lane 1: Non-transfected (–) HEK-293T whole cell lysate at 30 µg
Lane 2: Transfected (+) HEK-293T whole cell lysate at 30 µg
All lanes: HRP-conjugated anti-rabbit IgG antibody
Predicted band size: 27 kDa
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