Zobrazeno 1 - 10
of 83
pro vyhledávání: '"R. E. Gaines Das"'
Autor:
R. E. Gaines Das, P. L. Storring
Publikováno v:
Journal of Endocrinology. 171:119-129
The fourth International Standard for Human Urinary FSH and LH (IS; in ampoules coded 98/704) was compared with the third International Standard for Urinary FSH and LH (IS 71/264) by 10 laboratories in nine countries, using FSH and LH in vivo bioassa
Publikováno v:
Journal of Endocrinology. 150:401-412
Assays have been developed for the isoforms of erythropoietin (EPO) based on their binding to eight different lectins. These assays were used to compare the isoform compositions of two preparations of human urinary EPO (uEPO) and four preparations of
Autor:
R. E. Gaines Das, P. L. Storring
Publikováno v:
Journal of Endocrinology. 138:345-359
The second International Standard for Human Pituitary LH (in ampoules coded 80/552; 2nd IS) and LH 81/535 (prepared in the same way as the 2nd IS from the same LH preparation) were compared with the International Reference Preparation of Human Pituit
Autor:
A. F. Bristow, Glenys A. Tennent, Mark B. Pepys, R. E. Gaines-Das, N. Buttress, J. R. Gallimore
Publikováno v:
Clinical Endocrinology. 38:361-366
Summary OBJECTIVE Thyroxine binding globulin is the major thyroid hormone binding and transport protein of the plasma, and its quantitative estimation is therefore of clinical importance. The objectives of the present study were to prepare and ampoul
Autor:
R. E. Gaines Das, P. L. Storring
Publikováno v:
Journal of Endocrinology. 134:459-484
The International Standard (IS) for Recombinant DNA-Derived (rDNA) Erythropoietin (EPO) (in ampoules coded 87/684) and three other rDNA EPO preparations in ampoules coded 87/690, 87/696 and 88/574 respectively, were compared with two preparations of
Publikováno v:
The Journal of Automatic Chemistry
This report describes the results of a collaborative study organized by a joint working group of the IFCC and WHO and involving nine manufacturers of TSH immunometric assay kits. The study was designed to determine whether a calibrator with a common
Publikováno v:
Developments in biologicals. 111
A pre-validation study was carried out, by six laboratories from six countries, of two physicochemical methods for predicting the in vivo biological potency of recombinant follicle stimulating hormone (follitropin beta), based on quantitative measure
Autor:
R E, Gaines Das
Publikováno v:
Developments in biologicals. 107
Underlying the design of any assay and further, interpretation of the results, are multitudes of assumptions and implications, ranging from 'biological' assumptions about the nature of the assay system and its response to the materials assayed to 'st
Publikováno v:
Developments in biological standardization. 101
Ensuring the reliability and precision of assay results requires careful attention to assay design. In this case study we describe validation studies of an in vitro assay for botulinum neurotoxin type A based on its endopeptidase activity towards imm
Autor:
P L, Storring, R J, Tiplady, R E, Gaines Das, B E, Stenning, A, Lamikanra, B, Rafferty, J, Lee
Publikováno v:
British journal of haematology. 100(1)
Epoetin alfa and beta are the two forms of recombinant DNA-derived erythropoietin (rEPO), both synthesized in Chinese hamster ovary cells, which are used for the treatment of erythropoietin (EPO)-responsive anaemias. Several batches of each of these