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BioMetallics Inc elisa analysis software
Elisa Analysis Software, supplied by BioMetallics Inc, 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/elisa+data+analysis+software/elisa+analysis+software/pm07914404-50-34-38
Average 90 stars, based on 1 article reviews
elisa analysis software - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Purification:

Article Title: Measurement of interleukin 15.
Article Snippet: Interleukin 15 (IL-15) is a small helical cytokine that was first characterized by its ability to stimulate proliferation of the murine T cell line CTLL-2, but is now known to have activity on a variety of cell types.. This unit describes two protocols that can be used to measure IL-15 in culture supernatants and serum samples.. The first method (see Basic Protocol) uses an enzyme-linked immunosorbent assay (ELISA) that is specific for human IL-15, although it can also detect simian IL-15.

Recombinant:

Article Title: Measurement of interleukin 15.
Article Snippet: Interleukin 15 (IL-15) is a small helical cytokine that was first characterized by its ability to stimulate proliferation of the murine T cell line CTLL-2, but is now known to have activity on a variety of cell types.. This unit describes two protocols that can be used to measure IL-15 in culture supernatants and serum samples.. The first method (see Basic Protocol) uses an enzyme-linked immunosorbent assay (ELISA) that is specific for human IL-15, although it can also detect simian IL-15.

Enzyme-linked Immunosorbent Assay:

Article Title: Measurement of interleukin 15.
Article Snippet: Interleukin 15 (IL-15) is a small helical cytokine that was first characterized by its ability to stimulate proliferation of the murine T cell line CTLL-2, but is now known to have activity on a variety of cell types.. This unit describes two protocols that can be used to measure IL-15 in culture supernatants and serum samples.. The first method (see Basic Protocol) uses an enzyme-linked immunosorbent assay (ELISA) that is specific for human IL-15, although it can also detect simian IL-15.

Article Title: Reversal of P-glycoprotein-mediated multidrug resistance by pure anti-oestrogens and novel tamoxifen derivatives.
Article Snippet: In this study the ability of five novel anti-oestrogens [Ciodotamoxifen, pyrrolidino-C iodotamoxifen, ethyl bromide tamoxifen (EBTx), ICI 164,384 (ICI 164) and ICI 182,780] to alter drug toxicity to multidrug resistant cell lines have been compared.. The effect of these compounds on ATPdependent vinblastine (VBL) transport was also tested using inside-out vesicles (IOV) prepared from highly P-glycoprotein (Pgp)-expressing CCRF-CEM/VBL roa, cells.. The pure anti-oestrogen ICI 164 was most effective, enhancing doxorubicin and VBL toxicity to MCF-7Adr cells 25and 35fold, respectively, and was also the best inhibitor of ATP-dependent [‘H]VBL accumulation by IOV.

Software:

Article Title: Measurement of interleukin 15.
Article Snippet: Interleukin 15 (IL-15) is a small helical cytokine that was first characterized by its ability to stimulate proliferation of the murine T cell line CTLL-2, but is now known to have activity on a variety of cell types.. This unit describes two protocols that can be used to measure IL-15 in culture supernatants and serum samples.. The first method (see Basic Protocol) uses an enzyme-linked immunosorbent assay (ELISA) that is specific for human IL-15, although it can also detect simian IL-15.

Article Title: Reversal of P-glycoprotein-mediated multidrug resistance by pure anti-oestrogens and novel tamoxifen derivatives.
Article Snippet: In this study the ability of five novel anti-oestrogens [Ciodotamoxifen, pyrrolidino-C iodotamoxifen, ethyl bromide tamoxifen (EBTx), ICI 164,384 (ICI 164) and ICI 182,780] to alter drug toxicity to multidrug resistant cell lines have been compared.. The effect of these compounds on ATPdependent vinblastine (VBL) transport was also tested using inside-out vesicles (IOV) prepared from highly P-glycoprotein (Pgp)-expressing CCRF-CEM/VBL roa, cells.. The pure anti-oestrogen ICI 164 was most effective, enhancing doxorubicin and VBL toxicity to MCF-7Adr cells 25and 35fold, respectively, and was also the best inhibitor of ATP-dependent [‘H]VBL accumulation by IOV.

Concentration Assay:

Article Title: Reversal of P-glycoprotein-mediated multidrug resistance by pure anti-oestrogens and novel tamoxifen derivatives.
Article Snippet: In this study the ability of five novel anti-oestrogens [Ciodotamoxifen, pyrrolidino-C iodotamoxifen, ethyl bromide tamoxifen (EBTx), ICI 164,384 (ICI 164) and ICI 182,780] to alter drug toxicity to multidrug resistant cell lines have been compared.. The effect of these compounds on ATPdependent vinblastine (VBL) transport was also tested using inside-out vesicles (IOV) prepared from highly P-glycoprotein (Pgp)-expressing CCRF-CEM/VBL roa, cells.. The pure anti-oestrogen ICI 164 was most effective, enhancing doxorubicin and VBL toxicity to MCF-7Adr cells 25and 35fold, respectively, and was also the best inhibitor of ATP-dependent [‘H]VBL accumulation by IOV.

Control:

Article Title: Reversal of P-glycoprotein-mediated multidrug resistance by pure anti-oestrogens and novel tamoxifen derivatives.
Article Snippet: In this study the ability of five novel anti-oestrogens [Ciodotamoxifen, pyrrolidino-C iodotamoxifen, ethyl bromide tamoxifen (EBTx), ICI 164,384 (ICI 164) and ICI 182,780] to alter drug toxicity to multidrug resistant cell lines have been compared.. The effect of these compounds on ATPdependent vinblastine (VBL) transport was also tested using inside-out vesicles (IOV) prepared from highly P-glycoprotein (Pgp)-expressing CCRF-CEM/VBL roa, cells.. The pure anti-oestrogen ICI 164 was most effective, enhancing doxorubicin and VBL toxicity to MCF-7Adr cells 25and 35fold, respectively, and was also the best inhibitor of ATP-dependent [‘H]VBL accumulation by IOV.



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