Fast track antibodies constitute a diverse group of products that have been released to accelerate your research, but are not yet fully characterized. They have all been affinity purified and show high titre values against the immunizing peptide (by ELISA).
Use at an assay dependent concentration. : This antibody gave a positive result in ELISA against the immunizing peptide (ab73368).
Use a concentration of 1 µg/ml.
Use a concentration of 5 µg/ml. Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
Induces an innate immunity to viral infections by preventing the accumulation of viral RNAs in the cytoplasm. Seems to recruit the RNA processing exosome to degrade the target RNAs. Inhibits alphavirus and filovirus replication.
ADP ribosyltransferase diphtheria toxin like 13 antibody
ZC3HAV 1 antibody
ZC3HDC 2 antibody
Zinc finger antiviral protein antibody
Zinc finger CCCH domain containing protein 2 antibody
Zinc finger CCCH domain-containing antiviral protein 1 antibody
Zinc finger CCCH domain-containing protein 2 antibody
Zinc finger CCCH type antiviral 1 antibody
Zinc finger CCCH type antiviral protein 1 antibody
Zinc finger CCCH-type antiviral protein 1 antibody
This Fast-Track antibody is not yet fully characterised. These images represent
inconclusive preliminary data.
Immunocytochemistry/ Immunofluorescence - Anti-Zinc finger antiviral protein antibody (ab73369)
ICC/IF image of ab73369 stained HeLa cells. The cells were 4% PFA fixed (10 min), permabilised in 0.1% PBS-Tween (20 min) and incubated with the antibody (ab73369, 1µg/ml) for 1h at room temperature. 1%BSA / 10% normal goat serum / 0.3M glycine was used to block non-specific protein-protein interactions. The secondary antibody (green) was Alexa Fluor® 488 goat anti-rabbit IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red). DAPI was used to stain the cell nuclei (blue). This antibody also gave a positive IF result in 100$% methanol fixed (5 mins) HePG2 and MCF7 cells. However, this Fast-Track antibody is not yet fully characterised. This image represents inconclusive preliminary data.
IHC image of Zinc finger antiviral protein staining in Human Normal Kidney FFPE section, performed on a BondTM system using the standard protocol F. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH6, epitope retrieval solution 1) for 20 mins. The section was then incubated with ab73369, 5µg/ml, for 15 mins at room temperature and detected using an HRP conjugated compact polymer system. DAB was used as the chromogen. The section was then counterstained with haematoxylin and mounted with DPX.
Liu CH et al. Battle between influenza A virus and a newly identified antiviral activity of the PARP-containing ZAPL protein. Proc Natl Acad Sci U S A112:14048-53 (2015).
Read more (PubMed: 26504237) »
Gläsker S et al. The alternate triad motif of the poly(ADP-ribose) polymerase-like domain of the human zinc finger antiviral protein is essential for its antiviral activity. J Gen Virol95:816-22 (2014).
Read more (PubMed: 24457973) »