immunoabsorbent

immunoabsorbent

[im′yənō′absôr′bənt]
a gel or other inert substance used to absorb antibodies from a solution or to purify them.

immunoabsorbent

, immunoabsorbant (im?yu-no-ab-sor'bent, im-u?no-) [ immuno- + absorbent] Immunosorbent.

immunoabsorbent

a preparation of antigen attached to a solid support or antigen in an insoluble form, which absorbs homologous antibodies from a mixture of immunoglobulins. See immunosorbent, elisa.
References in periodicals archive ?
To determine the rate of bone formation, the bone alkaline phosphatase (BAP) was measured in serum using a competitive immunoabsorbent assay specific for BAP (Metra Biosystems Alkphase-BTM , Mountain View, California).
Commercially available enzyme linked immunoabsorbent (ELISA) kits, with confirmatory testing by gas chromatography/mass spectometry were used for 6 of the drugs.
Interleukin-6 (IL-6) and soluble intercellular adhesion molecule-1 (sICAM-1) were measured in systemic plasma by enzyme-linked immunoabsorbent assays (ELISA) kits.
Urinary albumin concentration was measured by enzyme-linked immunoabsorbent assay using an anti-rat albumin antibody and 24 h protein excretion was calculated by multiplying the urinary protein excretion by the 24 h urine volume.
beta] and IL-6 by sandwich enzyme linked immunoabsorbent assay (ELISA): Aliquots of 100 [micro]l from collected serum samples or standard proteins of [IL-1.
in Pomona, California, for screening using enzyme-linked immunoabsorbent assays followed by verification of positive samples with mass spectral detection using liquid chromatography/mass spectrometry.
Detection of attograms of antigen by a high-sensitivity enzyme-linked immunoabsorbent assay (HSELISA) using a fluorogenic substrate.
The accuracy of the enzyme-linked immunoabsorbent assay Ddimer test in the diagnosis of pulmonary embolism: a meta-analysis.
Urinary albumin concentrations were measured by enzyme-linked immunoabsorbent assay using an anti-rat albumin antibody and 241i urinary albumin excretion was calculated by multiplying the urinary protein excretion by the 24 h urine volume.
Current state of the art tuberculosis detection technologies rely mainly on using DNA signatures and polymerase chain reaction (PCR) or anti-body based enzyme-linked immunoabsorbent (ELISA) assays, both of which require many hours to produce results and ELISA does so with relatively low confidence because of the low specificity of the assays.
All of the products are ELISA kits: quantitative, "sandwich" enzyme-linked, immunoabsorbent assays for the detection of biologically active cytokines from blood serum, plasma and culture supernatant samples.
Detection of poultry and pork in cooked and canned meats by enzyme-linked immunoabsorbent assays, Journal Association of Offal Analytical Chemistry 71: 406-9.