Application
Western blot analysis of anti-H1L Mab (SG071115B) in recombinant pGEX-H1L protein. H1L(arrow) was detected using the purified Mab (1:60 dilution).Application
Western blot analysis of anti-H1L Mab (SG071115A) in recombinant H1L protein. H1L(arrow) was detected using the purified Mab (1:60 dilution).| Product Name | H1L Antibody |
|---|---|
| Antibody Type | Primary Antibodies |
| Antigen Alias | Late protein H1 |
| Clonality | Monoclonal |
|---|---|
| Isotype | IgG2a |
| Clone Number | 20CT26.44.10.3 / 20CT26.44.10.14 |
| Host Species | Mouse |
| Tested Applications | WB |
| WB:1:100-500 |
|
| Species Reactivity | Human |
| Concentration | 1mg/ml |
| Alternative Names | Late protein H1 |
|---|---|
| Molecular Weight(MW) | 19672 Da |
| Function | Serine/Tyrosine phosphatase which down-regulates cellular antiviral response by dephosphorylating activated host STAT1 and blocking interferon (IFN)-stimulated innate immune responses. Dephosphorylates the A17 protein (By similarity) |
| Tissue Specificity | Purified recombinant H1L fusion protein was used to produced this monoclonal antibody. |
| Cellular Localization | Virion (By similarity). Host cytoplasm (By similarity). Note=Approximately 200 molecules of H1 are packaged within the virion and are essential for the viability of the virus (By similarity) |
Application
Western blot analysis of anti-H1L Mab (SG071115B) in recombinant pGEX-H1L protein. H1L(arrow) was detected using the purified Mab (1:60 dilution).
Application
Western blot analysis of anti-H1L Mab (SG071115A) in recombinant H1L protein. H1L(arrow) was detected using the purified Mab (1:60 dilution).| Application Notes | WB:1:100-500 |
|---|
| Form | Liquid |
|---|---|
| Storage Instructions | For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles. |
| Storage Buffer | Purified monoclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS. |
