scholarly journals Bound/free separation methods in steroid enzyme immunoassay with monoclonal antibody.

1988 ◽  
Vol 36 (9) ◽  
pp. 3525-3531 ◽  
Author(s):  
HIROSHI HOSODA ◽  
REIKO TSUKAMOTO ◽  
SAKIKO TAMURA ◽  
TOSHIO NAMBARA
Keyword(s):  
Monoclonal Antibody ◽  
Enzyme Immunoassay

Development of a Monoclonal Antibody-Based Enzyme Immunoassay for the Pyrethroid Insecticide Deltamethrin

2010 ◽  
Vol 58 (14) ◽  
pp. 8189-8195 ◽  
Author(s):  
Ye Kong ◽  
Qi Zhang ◽  
Wen Zhang ◽  
Shirley J. Gee ◽  
Peiwu Li
Keyword(s):  
Monoclonal Antibody ◽  
Enzyme Immunoassay ◽  
Pyrethroid Insecticide

scholarly journals An enzyme immunoassay system with a monoclonal antibody for the determination of 11-deoxycortisol.

1987 ◽  
Vol 35 (4) ◽  
pp. 1497-1502 ◽  
Author(s):  
HIROSHI HOSODA ◽  
SAKIKO TAMURA ◽  
REIKO TSUKAMOTO ◽  
NORIHIRO KOBAYASHI ◽  
JUN-ICHI SAWADA ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
Enzyme Immunoassay

scholarly journals Determination of Domoic Acid in Japanese Mussels by Enzyme Immunoassay

2000 ◽  
Vol 83 (6) ◽  
pp. 1384-1386 ◽  
Author(s):  
Kentaro Kawatsu ◽  
Yonekazu Hamano ◽  
Tamao Noguchi
Keyword(s):  
Monoclonal Antibody ◽  
Enzyme Immunoassay ◽  
Domoic Acid ◽  
Immunoaffinity Chromatography ◽  
Shellfish Poisoning ◽  
Mussel Tissue ◽  
Blue Mussels ◽  
Amnesic Shellfish Poisoning ◽  
Low Concentrations

Abstract Ten samples of commercial blue mussels (Mytilus edulis) from Japan were analyzed for domoic acid by an indirect competitive enzyme immunoassay (idc–EIA) based on an anti-domoic acid monoclonal antibody. Domoic acid was found in all samples at low concentrations (0.11–1.81 ng/g mussel tissue). The presence of domoic acid was confirmed by liquid chromatography coupled with immunoaffinity chromatography using an anti-domoic acid monoclonal antibody as ligand. To our knowledge, this is the first reported detection of domoic acid, a causative agent of amnesic shellfish poisoning, in Japanese mussels.

An accelerated enzyme immunoassay for human choriogonadotropin in urine, involving reflow of specimen through capillary tubes.

1987 ◽  
Vol 33 (4) ◽  
pp. 498-501 ◽  
Author(s):  
H M Chandler ◽  
S A Fuller ◽  
C H Nakagawa ◽  
P A Nagainis ◽  
J G Hurrell
Keyword(s):  
Monoclonal Antibody ◽  
Monoclonal Antibodies ◽  
Enzyme Immunoassay ◽  
Test Specimen ◽  
Capillary Tube ◽  
Test Procedure ◽  
Beta Subunit ◽  
Sensitive Assay ◽  
Substrate Solution ◽  
Human Choriogonadotropin

Abstract A very rapid and sensitive assay for human choriogonadotropin (hCG) has been developed involving two beta-subunit-specific monoclonal antibodies. In the assay the test specimen is passed backward and forward (reflow) through a monoclonal-antibody-coated capillary tube for 1 min, then incubated for 1 min with a second monoclonal antibody conjugated to urease (EC 3.5.1.5). After addition of a urease substrate solution, 10 int. units of hCG per liter can be detected visually within 5 min, which compares very favorably with other currently available hCG assay procedures. Advantages of the reflow/capillary tube assay system and optimization of the test procedure are discussed.

Two-site enzyme immunoassay of CD4 and CD8 molecules on the surface of T lymphocytes from healthy subjects and HIV-1-infected patients

1994 ◽  
Vol 40 (1) ◽  
pp. 30-37 ◽  
Author(s):  
D Carriere ◽  
C Fontaine ◽  
A M Berthier ◽  
A M Rouquette ◽  
P Carayon ◽  
...  
Keyword(s):  
Monoclonal Antibody ◽  
T Lymphocytes ◽  
Enzyme Immunoassay ◽  
Cd8 T Cells ◽  
Envelope Glycoprotein ◽  
Healthy Subjects ◽  
Gp 120 ◽  
Highly Sensitive ◽  
One Step ◽  
Hiv 1

Abstract A highly sensitive two-site enzyme immunoassay (Capcellia) was developed to determine the concentration of CD4 and CD8 molecules expressed on the surface of human T lymphocytes. This assay, performed in one step (20 min), involves the specific immunocapture of T lymphocytes and reaction of the CD4 or CD8 molecules with an enzyme-labeled monoclonal antibody (mAb). The results were expressed as molar concentrations of the T-cell markers on the basis of results obtained with calibrated CD4 and CD8 standards. The assay was sensitive enough to detect 0.4 pmol/L CD4 or 0.8 pmol/L CD8, which corresponded to approximately 20 x 10(6) CD4+ or CD8+ T cells per liter of blood. Mean concentrations in healthy adults were 17.2 pmol/L for CD4 and 22.1 pmol/L for CD8. The CD4 concentration was < 8 pmol/L in 50% of HIV-1-infected patients and in 95% of AIDS patients. Given the epitopic specificity of the mAb to CD4 we used, these values correspond to the concentration of CD4 molecules free of envelope glycoprotein (gp)120.

Sign in / Sign up

Export Citation Format

Share Document