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Specific elisa

Manufactured by Alpha Diagnostic

Specific ELISA is a laboratory equipment used for enzyme-linked immunosorbent assay (ELISA) testing. It is designed to detect and measure specific target analytes in a sample. The core function of Specific ELISA is to quantify the presence and concentration of a particular substance or molecule of interest through a series of immunochemical reactions and colorimetric detection.

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2 protocols using specific elisa

1

Generation of Anti-Siglec-15 Monoclonal Antibodies

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To generate the mAbs, NZB/NZW F1 mice were immunized with mouse Siglec-15 Fc fusion protein in Freund’s adjuvants (Sigma-Aldrich, St Louis, MO) using protocols as previously described44 (link),45 (link). Hybridoma clones (m01 and m03) were screened by mouse Siglec-15 Fc specific ELISA as well as flow cytometry using 293T-S15+ cells. A different panel of Siglec-15 hybridomas were also generated by the immunization of Siglec-15 KO mice with human Siglec-15 Fc in complete Freund’s adjuvant followed by i.p. injection of anti-CD40/GM-CSF (BioLegend), and then boosted with Sigelc15 Fc in incomplete Freund’s adjuvant. Hybridoma clones (5G12 and IH3) were selected based on their specificity to both mouse and human Siglec-15.
Mouse tissues and tumors were excised, fixed with formalin, embedded with paraffin, and stained with hematoxylin and eosin. Tissue inflammatory status was evaluated in a blind manner by pathologists. Anti-nuclear antigens Ig and anti-double stranded DNA IgG in the serum of mice were analyzed by specific ELISA (Alpha Diagnostic International, San Antonio, TX).
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2

Generation of Anti-Siglec-15 Monoclonal Antibodies

Check if the same lab product or an alternative is used in the 5 most similar protocols
To generate the mAbs, NZB/NZW F1 mice were immunized with mouse Siglec-15 Fc fusion protein in Freund’s adjuvants (Sigma-Aldrich, St Louis, MO) using protocols as previously described44 (link),45 (link). Hybridoma clones (m01 and m03) were screened by mouse Siglec-15 Fc specific ELISA as well as flow cytometry using 293T-S15+ cells. A different panel of Siglec-15 hybridomas were also generated by the immunization of Siglec-15 KO mice with human Siglec-15 Fc in complete Freund’s adjuvant followed by i.p. injection of anti-CD40/GM-CSF (BioLegend), and then boosted with Sigelc15 Fc in incomplete Freund’s adjuvant. Hybridoma clones (5G12 and IH3) were selected based on their specificity to both mouse and human Siglec-15.
Mouse tissues and tumors were excised, fixed with formalin, embedded with paraffin, and stained with hematoxylin and eosin. Tissue inflammatory status was evaluated in a blind manner by pathologists. Anti-nuclear antigens Ig and anti-double stranded DNA IgG in the serum of mice were analyzed by specific ELISA (Alpha Diagnostic International, San Antonio, TX).
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