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    ELISA SYSTEMS Pty Ltd cchfv elisa systems
    Serological assays.
    Cchfv Elisa Systems, supplied by ELISA SYSTEMS Pty Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cchfv+elisa+systems/cchfv+elisa+systems/pmc08303759-82-9-10
    Average 90 stars, based on 1 article reviews
    cchfv elisa systems - by Bioz Stars, 2026-11
    90/100 stars

    Images

    1) Product Images from "Deciphering Antibody Responses to Orthonairoviruses in Ruminants"

    Article Title: Deciphering Antibody Responses to Orthonairoviruses in Ruminants

    Journal: Microorganisms

    doi: 10.3390/microorganisms9071493

    Serological assays.
    Figure Legend Snippet: Serological assays.

    Techniques Used: Indirect ELISA, Enzyme-linked Immunosorbent Assay, Fluorescence, Control

    Euroimmun iIFA with sheep NSDV antisera: The results obtained with the serum of an infected sheep (P2) are presented as an example together with the results for the control sheep (O2). A specific staining is demonstrated for cells expressing CCHFV GPC ( B ) as well as CCHFV N ( D ) for P2. All controls (cell control: ( E ); serum prior to infection: ( A , C )) did not lead to a positive signal. The control sheep O2 did not test positive in any condition ( F – J ).
    Figure Legend Snippet: Euroimmun iIFA with sheep NSDV antisera: The results obtained with the serum of an infected sheep (P2) are presented as an example together with the results for the control sheep (O2). A specific staining is demonstrated for cells expressing CCHFV GPC ( B ) as well as CCHFV N ( D ) for P2. All controls (cell control: ( E ); serum prior to infection: ( A , C )) did not lead to a positive signal. The control sheep O2 did not test positive in any condition ( F – J ).

    Techniques Used: Infection, Control, Staining, Expressing

    Euroimmun iIFA with cattle NSDV antisera: Results for one infected calf (Q6) are exemplarily presented together with the results for the mock control calf (S2). A specific staining is demonstrated for cells expressing CCHFV GPC ( B ). All controls (cell control: ( C ); serum prior infection: ( A ) did not lead to a positive signal. The control calf S2 did not test positive under any circumstances ( D – F ).
    Figure Legend Snippet: Euroimmun iIFA with cattle NSDV antisera: Results for one infected calf (Q6) are exemplarily presented together with the results for the mock control calf (S2). A specific staining is demonstrated for cells expressing CCHFV GPC ( B ). All controls (cell control: ( C ); serum prior infection: ( A ) did not lead to a positive signal. The control calf S2 did not test positive under any circumstances ( D – F ).

    Techniques Used: Infection, Control, Staining, Expressing

    Specificity and sensitivity of HAZV, DUGV, and NSDV assays: Panel ( A ) shows the proportion of positive tested sera within a specific assay in relation to all sera following infections/immunizations with the same challenge virus, which were at least positive in one homologous virus-specific test. Exemplarily, seven sera from the DUGV studies were tested positive in the NSDV PRNT out of ten animals with DUGV antibodies detectable via any DUGV assay, leading to a bar of approx. 70% length. Panel ( B ) visualizes the ranking order of sensitivity and specificity for all diagnostic assays, with highest sensitivity achieved by PRNT and highest specificity by ELISA.
    Figure Legend Snippet: Specificity and sensitivity of HAZV, DUGV, and NSDV assays: Panel ( A ) shows the proportion of positive tested sera within a specific assay in relation to all sera following infections/immunizations with the same challenge virus, which were at least positive in one homologous virus-specific test. Exemplarily, seven sera from the DUGV studies were tested positive in the NSDV PRNT out of ten animals with DUGV antibodies detectable via any DUGV assay, leading to a bar of approx. 70% length. Panel ( B ) visualizes the ranking order of sensitivity and specificity for all diagnostic assays, with highest sensitivity achieved by PRNT and highest specificity by ELISA.

    Techniques Used: Virus, Diagnostic Assay, Enzyme-linked Immunosorbent Assay

    Related Articles

    Immunofluorescence:

    Article Title: Deciphering Antibody Responses to Orthonairoviruses in Ruminants
    Article Snippet: .. Furthermore, all NSDV antisera were run in three different CCHFV ELISA systems and one indirect immunofluorescence test. .. The multispecies double antigen ELISA (IDVet, Grabels, France) was applied according to the manufacturers’ instructions.



    Similar Products

    cchfv elisa systems  (ELISA SYSTEMS Pty Ltd)
    90
    ELISA SYSTEMS Pty Ltd cchfv elisa systems
    Serological assays.
    Cchfv Elisa Systems, supplied by ELISA SYSTEMS Pty Ltd, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cchfv+elisa+systems/cchfv+elisa+systems/pmc08303759-82-9-10
    Average 90 stars, based on 1 article reviews
    cchfv elisa systems - by Bioz Stars, 2026-11
    90/100 stars
    		  Buy from Supplier

    Image Search Results


    Serological assays.

    Journal: Microorganisms

    Article Title: Deciphering Antibody Responses to Orthonairoviruses in Ruminants

    doi: 10.3390/microorganisms9071493

    Figure Lengend Snippet: Serological assays.

    Article Snippet: Furthermore, all NSDV antisera were run in three different CCHFV ELISA systems and one indirect immunofluorescence test.

    Techniques: Indirect ELISA, Enzyme-linked Immunosorbent Assay, Fluorescence, Control

    Euroimmun iIFA with sheep NSDV antisera: The results obtained with the serum of an infected sheep (P2) are presented as an example together with the results for the control sheep (O2). A specific staining is demonstrated for cells expressing CCHFV GPC ( B ) as well as CCHFV N ( D ) for P2. All controls (cell control: ( E ); serum prior to infection: ( A , C )) did not lead to a positive signal. The control sheep O2 did not test positive in any condition ( F – J ).

    Journal: Microorganisms

    Article Title: Deciphering Antibody Responses to Orthonairoviruses in Ruminants

    doi: 10.3390/microorganisms9071493

    Figure Lengend Snippet: Euroimmun iIFA with sheep NSDV antisera: The results obtained with the serum of an infected sheep (P2) are presented as an example together with the results for the control sheep (O2). A specific staining is demonstrated for cells expressing CCHFV GPC ( B ) as well as CCHFV N ( D ) for P2. All controls (cell control: ( E ); serum prior to infection: ( A , C )) did not lead to a positive signal. The control sheep O2 did not test positive in any condition ( F – J ).

    Article Snippet: Furthermore, all NSDV antisera were run in three different CCHFV ELISA systems and one indirect immunofluorescence test.

    Techniques: Infection, Control, Staining, Expressing

    Euroimmun iIFA with cattle NSDV antisera: Results for one infected calf (Q6) are exemplarily presented together with the results for the mock control calf (S2). A specific staining is demonstrated for cells expressing CCHFV GPC ( B ). All controls (cell control: ( C ); serum prior infection: ( A ) did not lead to a positive signal. The control calf S2 did not test positive under any circumstances ( D – F ).

    Journal: Microorganisms

    Article Title: Deciphering Antibody Responses to Orthonairoviruses in Ruminants

    doi: 10.3390/microorganisms9071493

    Figure Lengend Snippet: Euroimmun iIFA with cattle NSDV antisera: Results for one infected calf (Q6) are exemplarily presented together with the results for the mock control calf (S2). A specific staining is demonstrated for cells expressing CCHFV GPC ( B ). All controls (cell control: ( C ); serum prior infection: ( A ) did not lead to a positive signal. The control calf S2 did not test positive under any circumstances ( D – F ).

    Article Snippet: Furthermore, all NSDV antisera were run in three different CCHFV ELISA systems and one indirect immunofluorescence test.

    Techniques: Infection, Control, Staining, Expressing

    Specificity and sensitivity of HAZV, DUGV, and NSDV assays: Panel ( A ) shows the proportion of positive tested sera within a specific assay in relation to all sera following infections/immunizations with the same challenge virus, which were at least positive in one homologous virus-specific test. Exemplarily, seven sera from the DUGV studies were tested positive in the NSDV PRNT out of ten animals with DUGV antibodies detectable via any DUGV assay, leading to a bar of approx. 70% length. Panel ( B ) visualizes the ranking order of sensitivity and specificity for all diagnostic assays, with highest sensitivity achieved by PRNT and highest specificity by ELISA.

    Journal: Microorganisms

    Article Title: Deciphering Antibody Responses to Orthonairoviruses in Ruminants

    doi: 10.3390/microorganisms9071493

    Figure Lengend Snippet: Specificity and sensitivity of HAZV, DUGV, and NSDV assays: Panel ( A ) shows the proportion of positive tested sera within a specific assay in relation to all sera following infections/immunizations with the same challenge virus, which were at least positive in one homologous virus-specific test. Exemplarily, seven sera from the DUGV studies were tested positive in the NSDV PRNT out of ten animals with DUGV antibodies detectable via any DUGV assay, leading to a bar of approx. 70% length. Panel ( B ) visualizes the ranking order of sensitivity and specificity for all diagnostic assays, with highest sensitivity achieved by PRNT and highest specificity by ELISA.

    Article Snippet: Furthermore, all NSDV antisera were run in three different CCHFV ELISA systems and one indirect immunofluorescence test.

    Techniques: Virus, Diagnostic Assay, Enzyme-linked Immunosorbent Assay