Human CD169 ELISA Kit (SIGLEC-1)
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Human CD169 ELISA Kit (SIGLEC-1) is a Sandwich (quantitative) ELISA for the measurement of Human CD169 (SIGLEC-1) in Human in Cell/Tissue Extracts, Cell Culture Media, Biofluids samples.
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CD169, SN, SIGLEC1, Sialoadhesin, Sialic acid-binding Ig-like lectin 1, Siglec-1
- sELISA
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Sandwich ELISA - Human CD169 ELISA Kit (SIGLEC-1) (AB213757)
Human CD169 ELISA Kit (SIGLEC-1) (ab213757) Standard Curve.
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The Human CD169 Enzyme-Linked Immunosorbent Assay (ELISA) kit (SIGLEC-1) (ab213757) is designed for the quantitative measurement of Human CD169 in cell culture supernatants, cell lysates, serum and plasma (heparin, EDTA).
The ELISA kit is based on standard sandwich enzyme-linked immunosorbent assay technology. A monoclonal antibody from mouse specific for CD169/SIGLEC-1 has been pre-coated onto 96-well plates. Standards (Expression system for standard: NSO; Immunogen sequence: S20-Q1641) and test samples are added to the wells, a biotinylated detection polyclonal antibody from goat specific for CD169/SIGLEC-1 is added subsequently and then followed by washing with PBS or TBS buffer. Avidin-Biotin-Peroxidase Complex is added and unbound conjugates are washed away with PBS or TBS buffer. HRP substrate TMB is used to visualize HRP enzymatic reaction. TMB is catalyzed by HRP to produce a blue color product that changed into yellow after adding acidic stop solution. The density of yellow is proportional to the Human CD169/SIGLEC-1 amount of sample captured in plate.
SIGLEC-1, also known as Sialoadhesin or CD169, is a cell adhesion molecule found on the surface of certain cells of the immune system called macrophages. This gene is mapped to 20p13. It belongs to the immunoglobulin superfamily (IgSF). Since sialoadhesin binds sialic acids with its N-terminal IgV domain, it is also a member of the SIGLEC family. The localization and expression of SIGLEC-1 in humans has altered coincident with the evolutionary loss of Neu5Gc. SIGLEC-1-positive macrophages have a dual physiologic function. They act as innate 'flypaper' by preventing the systemic spread of lymph-borne pathogens and as critical gatekeepers at the lymph-tissue interface that facilitate the recognition of particulate antigens by B cells and initiate humoral immune responses.
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Proceedings of the National Academy of Sciences of the United States of America 121:e2402983121 PubMed39312669
2024
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