Cat#: | ORO-528 |
Product Name: | Recombinant Oropouche Virus Gn Protein, hFc-tagged |
Description: | Oropouche virus Gn protein was expressed in mammalian HEK293 cells. The transmembrane region of the protein has been replaced with mouse IgG Fc, via a glycine-serine linker. The purified protein is approximately 55kD on analysis by reducing SDS-PAGE. |
Gene: | Gn |
Species: | Oropouche virus |
Source: | HEK293 |
Synonyms: | Oropouche Virus Gn |
Formulation: | DPBS pH7.4 |
Concentration: | 0.42 mg/mL |
Purity: | Greater than 90% purity by SDS-PAGE. |
Storage: | Short Term Storage: +2 centigrade to +8 centigrade Long Term Storage: -80 centigrade |
Notes: | This product is intended for research and manufacturing uses only. It is not a diagnostic device. The user assumes all responsibility for care, custody and control of the material, including its disposal, in accordance with all regulations. |
Tags: | C-terminal human IgG1 Fc |
Freezing: | Can be frozen, but avoid multiple freeze/thaw cycles. |
Sequence Strain: | BeH759022, human clinical isolate |
Background: | Oropouche virus (OROV) is an RNA virus that belongs to the family Bunyaviridae. The virus can cause an acute febrile illness, with other symptoms similar to those reported for Dengue, Zika, and Chikungunya virus infection, including headache, myalgia, joint pain, nausea and vomiting. In some cases, OROV can cause a type of viral meningitis. In humans, OROV is transmitted by the biting midge culicoides paraensis, an insect vector that lives in urban areas and is widely distributed in South America. Since the virus was first isolated in 1955, OROV has caused 30 large scale epidemics in the Amazon region infecting at least 500,000 people. The incidence of Oropouche fever has now become widespread in Latin American countries where C. paraensis is present. Differential diagnosis of Oropouche virus infection from infection with Dengue, Zika or Chikungunya is recognised to be important, but there are few diagnostic assays available. Oropouche virus Gn protein is a type I integral transmembrane protein, which is further modified by N-linked glycosylation. Together with Gc protein it forms spikes on the virus particle and is essential for viral attachment and cell fusion. It has been described that for certain bunyaviruses, Gn and Gc are targeted by neutralizing antibodies |
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For research or industrial raw materials, not for personal medical use!
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