15 well slide Search Results


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Antibodies Inc msips4w10 hep 2 slides antibodies
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Antibodies Inc crithidia slides
16D2 cross‐reacts with dsDNA. 16D2 was tested by ELISA for binding to EBNA‐1 (A) and dsDNA (B). Binding to dsDNA was confirmed by immunostaining of the kinetoplast of <t>Crithidia</t> luciliae (C). Immunostaining of an isotype control MAb is shown in D (D). 16D2 was tested by ELISA for reactivity with a panel of antigens; Sm, LPS, BSA, and proteinase 3 (PR3) (E). Results are representative of three experiments. ELISA values were obtained in triplicate. Error bars indicate standard deviations of triplicate values.
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Antibodies Inc hep 2 slides
16D2 cross‐reacts with dsDNA. 16D2 was tested by ELISA for binding to EBNA‐1 (A) and dsDNA (B). Binding to dsDNA was confirmed by immunostaining of the kinetoplast of <t>Crithidia</t> luciliae (C). Immunostaining of an isotype control MAb is shown in D (D). 16D2 was tested by ELISA for reactivity with a panel of antigens; Sm, LPS, BSA, and proteinase 3 (PR3) (E). Results are representative of three experiments. ELISA values were obtained in triplicate. Error bars indicate standard deviations of triplicate values.
Hep 2 Slides, supplied by Antibodies Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ibidi GmbH 15-well μ-slide angiogenesis plates ibidi, germany
16D2 cross‐reacts with dsDNA. 16D2 was tested by ELISA for binding to EBNA‐1 (A) and dsDNA (B). Binding to dsDNA was confirmed by immunostaining of the kinetoplast of <t>Crithidia</t> luciliae (C). Immunostaining of an isotype control MAb is shown in D (D). 16D2 was tested by ELISA for reactivity with a panel of antigens; Sm, LPS, BSA, and proteinase 3 (PR3) (E). Results are representative of three experiments. ELISA values were obtained in triplicate. Error bars indicate standard deviations of triplicate values.
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ibidi GmbH 15 μ-slide-well – 80826
16D2 cross‐reacts with dsDNA. 16D2 was tested by ELISA for binding to EBNA‐1 (A) and dsDNA (B). Binding to dsDNA was confirmed by immunostaining of the kinetoplast of <t>Crithidia</t> luciliae (C). Immunostaining of an isotype control MAb is shown in D (D). 16D2 was tested by ELISA for reactivity with a panel of antigens; Sm, LPS, BSA, and proteinase 3 (PR3) (E). Results are representative of three experiments. ELISA values were obtained in triplicate. Error bars indicate standard deviations of triplicate values.
15 μ Slide Well – 80826, supplied by ibidi GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ibidi GmbH 15 μ-slide 8 well culture plates
16D2 cross‐reacts with dsDNA. 16D2 was tested by ELISA for binding to EBNA‐1 (A) and dsDNA (B). Binding to dsDNA was confirmed by immunostaining of the kinetoplast of <t>Crithidia</t> luciliae (C). Immunostaining of an isotype control MAb is shown in D (D). 16D2 was tested by ELISA for reactivity with a panel of antigens; Sm, LPS, BSA, and proteinase 3 (PR3) (E). Results are representative of three experiments. ELISA values were obtained in triplicate. Error bars indicate standard deviations of triplicate values.
15 μ Slide 8 Well Culture Plates, supplied by ibidi GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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16D2 cross‐reacts with dsDNA. 16D2 was tested by ELISA for binding to EBNA‐1 (A) and dsDNA (B). Binding to dsDNA was confirmed by immunostaining of the kinetoplast of <t>Crithidia</t> luciliae (C). Immunostaining of an isotype control MAb is shown in D (D). 16D2 was tested by ELISA for reactivity with a panel of antigens; Sm, LPS, BSA, and proteinase 3 (PR3) (E). Results are representative of three experiments. ELISA values were obtained in triplicate. Error bars indicate standard deviations of triplicate values.
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ibidi GmbH 15 μ-slide 8 well ibitreat
16D2 cross‐reacts with dsDNA. 16D2 was tested by ELISA for binding to EBNA‐1 (A) and dsDNA (B). Binding to dsDNA was confirmed by immunostaining of the kinetoplast of <t>Crithidia</t> luciliae (C). Immunostaining of an isotype control MAb is shown in D (D). 16D2 was tested by ELISA for reactivity with a panel of antigens; Sm, LPS, BSA, and proteinase 3 (PR3) (E). Results are representative of three experiments. ELISA values were obtained in triplicate. Error bars indicate standard deviations of triplicate values.
15 μ Slide 8 Well Ibitreat, supplied by ibidi GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ibidi GmbH 15 μ-slide 8 well chambers
16D2 cross‐reacts with dsDNA. 16D2 was tested by ELISA for binding to EBNA‐1 (A) and dsDNA (B). Binding to dsDNA was confirmed by immunostaining of the kinetoplast of <t>Crithidia</t> luciliae (C). Immunostaining of an isotype control MAb is shown in D (D). 16D2 was tested by ELISA for reactivity with a panel of antigens; Sm, LPS, BSA, and proteinase 3 (PR3) (E). Results are representative of three experiments. ELISA values were obtained in triplicate. Error bars indicate standard deviations of triplicate values.
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INYCOM Inc ecm-coated μ-slide 15 well 3d ibitreat plates
16D2 cross‐reacts with dsDNA. 16D2 was tested by ELISA for binding to EBNA‐1 (A) and dsDNA (B). Binding to dsDNA was confirmed by immunostaining of the kinetoplast of <t>Crithidia</t> luciliae (C). Immunostaining of an isotype control MAb is shown in D (D). 16D2 was tested by ELISA for reactivity with a panel of antigens; Sm, LPS, BSA, and proteinase 3 (PR3) (E). Results are representative of three experiments. ELISA values were obtained in triplicate. Error bars indicate standard deviations of triplicate values.
Ecm Coated μ Slide 15 Well 3d Ibitreat Plates, supplied by INYCOM Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Ibidi USA 15- well chamber slide
16D2 cross‐reacts with dsDNA. 16D2 was tested by ELISA for binding to EBNA‐1 (A) and dsDNA (B). Binding to dsDNA was confirmed by immunostaining of the kinetoplast of <t>Crithidia</t> luciliae (C). Immunostaining of an isotype control MAb is shown in D (D). 16D2 was tested by ELISA for reactivity with a panel of antigens; Sm, LPS, BSA, and proteinase 3 (PR3) (E). Results are representative of three experiments. ELISA values were obtained in triplicate. Error bars indicate standard deviations of triplicate values.
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ibidi GmbH micro-slide angiogenesis 15-well
16D2 cross‐reacts with dsDNA. 16D2 was tested by ELISA for binding to EBNA‐1 (A) and dsDNA (B). Binding to dsDNA was confirmed by immunostaining of the kinetoplast of <t>Crithidia</t> luciliae (C). Immunostaining of an isotype control MAb is shown in D (D). 16D2 was tested by ELISA for reactivity with a panel of antigens; Sm, LPS, BSA, and proteinase 3 (PR3) (E). Results are representative of three experiments. ELISA values were obtained in triplicate. Error bars indicate standard deviations of triplicate values.
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16D2 cross‐reacts with dsDNA. 16D2 was tested by ELISA for binding to EBNA‐1 (A) and dsDNA (B). Binding to dsDNA was confirmed by immunostaining of the kinetoplast of Crithidia luciliae (C). Immunostaining of an isotype control MAb is shown in D (D). 16D2 was tested by ELISA for reactivity with a panel of antigens; Sm, LPS, BSA, and proteinase 3 (PR3) (E). Results are representative of three experiments. ELISA values were obtained in triplicate. Error bars indicate standard deviations of triplicate values.

Journal: Immunity, Inflammation and Disease

Article Title: Mapping an epitope in EBNA‐1 that is recognized by monoclonal antibodies to EBNA‐1 that cross‐react with dsDNA

doi: 10.1002/iid3.119

Figure Lengend Snippet: 16D2 cross‐reacts with dsDNA. 16D2 was tested by ELISA for binding to EBNA‐1 (A) and dsDNA (B). Binding to dsDNA was confirmed by immunostaining of the kinetoplast of Crithidia luciliae (C). Immunostaining of an isotype control MAb is shown in D (D). 16D2 was tested by ELISA for reactivity with a panel of antigens; Sm, LPS, BSA, and proteinase 3 (PR3) (E). Results are representative of three experiments. ELISA values were obtained in triplicate. Error bars indicate standard deviations of triplicate values.

Article Snippet: Ready to use Crithidia slides (Antibodies Inc., Davis, CA) were immunostained with MAb, 16D2 at 10 μg/ml.

Techniques: Enzyme-linked Immunosorbent Assay, Binding Assay, Immunostaining, Control