Rabbit Recombinant Monoclonal Hepatitis D Virus antibody. Carrier free. Suitable for ICC/IF, WB and reacts with Transfected cell line samples.
pH: 7.4
Constituents: 100% PBS
ICC/IF | WB | |
---|---|---|
Transfected cell line | Tested | Tested |
Species | Dilution info | Notes |
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Species Transfected cell line | Dilution info 1/500 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Transfected cell line | Dilution info 1/5000 | Notes - |
Following virus entry into host cell, provides nuclear import of HDV RNPs thanks to its nuclear localization signal. Needs co-infection with hepatitis B virus to provide surface proteins, otherwise there is no packaging or budding. Packages the HDV ribonucleoprotein in hepatitis B virus empty particles. Interacts with both HDV genomic RNA and cytoplasmic tail of HBsAg. May inhibit viral RNA replication.
Hepatitis D Small delta antigen
Large delta antigen, L-HDAg, p27
Rabbit Recombinant Monoclonal Hepatitis D Virus antibody. Carrier free. Suitable for ICC/IF, WB and reacts with Transfected cell line 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 Hepatitis D Small delta antigen (SDAg) and Large delta antigen (LDAg) are essential proteins of the Hepatitis D virus (HDV) known for their involvement in the virus's replication and pathogenesis. The Small delta antigen weighs approximately 24 kDa and the Large delta antigen is about 195 kDa. These proteins are expressed in the cytoplasm and nucleus of infected liver cells where they perform distinct yet interconnected roles in the life cycle of HDV. SDAg facilitates viral replication while LDAg is important for virion assembly.
The Hepatitis D antigens Small and Large are part of a dynamic complex that plays a significant role in HDV infection. The Small delta antigen enhances the replication of viral RNA by interacting with the cellular machinery effectively hijacking the host cell's resources. In contrast the Large delta antigen mediates encapsidation processes that lead to the formation of new virions. This functional dichotomy within the antigens highlights their unique contributions to HDV persistence in the host organism.
Hepatitis D Small and Large delta antigens interface with cellular pathways that are critical for viral survival and propagation. The interferon signaling pathway is notably affected by these antigens as they manipulate host responses to favor HDV replication. Another impacted pathway includes the RNA interference pathway which is modulated by interactions between delta antigens and cellular proteins like Dicer. These interactions indicate the sophisticated strategies HDV employs to leverage host cellular pathways to its advantage.
The Hepatitis D Small and Large delta antigens are directly tied to Hepatitis D infection a severe form of viral hepatitis that can exacerbate the condition in individuals with concurrent Hepatitis B infection. The presence of LDAg correlates with disease progression and liver damage as it relates to chronic liver diseases such as cirrhosis and hepatocellular carcinoma. These delta antigens also interact with the Hepatitis B surface antigen facilitating virion assembly and enabling the HDV to propagate alongside HBV indicating their contribution to co-infection dynamics.
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.
Non-transfected (–) and transfected (+) Huh-7 whole cell extracts (30 μg) were separated by 12% SDS-PAGE, and the membrane was blotted with Hepatitis D virus Large data + Small delta protein antibody [HL1055] (ab308391) diluted at 1/5000. The HRP-conjugated anti-rabbit IgG antibody was used to detect the primary antibody.
All lanes: Western blot - Anti-Hepatitis D virus Large delta + Small delta protein antibody [HL1055] (ab308391) at 1/5000 dilution
Lane 1: Non-transfected (–) Huh-7 whole cell extracts at 30 µg
Lanes 2 - 3: Transfected (+) Huh-7 whole cell extracts at 30 µg
All lanes: HRP-conjugated anti-rabbit IgG antibody
For immunofluorescence analysis, mock and transfected HEK293T cells were fixed in 4% paraformaldehyde at room temperature for 15 minutes and permeabilized for detection of Hepatitis D virus Large delta + Small delta protein using ab308391 at 1/500 dilution (green). Blue: Fluoroshield with DAPI.
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