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Determination of clenbuterol from pork samples using surface molecularly imprinted polymers as the selective sorbents for microextraction in packed syringe.

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Polyamine-like immunoreactivity in rat neurons

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Specificities of five kinds of antisera produced against crude drugs, pinella tuber, hoelen, glycyrrhizae radix, trichosanthes root and panax ginseng.

Five kinds of rabbit antisera produced againstfive kinds of crude drugs, Pinella Tuber, Glycyrrhizae Radix (GR), Trichosanthes Root, Hoelen, and Panax Ginseng, and five kinds of extracts of the same crude drugs were prepared, finding characteristic antigen specific to the corresponding antiserum.
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Determination of thiocyanate metabolite of sodium nitroprusside in serum by spectrophotometry.

A sensitive, reproducible and rapid method for the spectrophotometric determination of thiocyanate, the metabolite of sodium nitroprusside, was developed. Acetonitrile was used to remove protein in…
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Immunoelectron Microscopic Study for Polyamines

It is demonstrated that PA are predominantly located on free and attached ribosomes of the rough endoplasmic reticulum in the neurons of the lateral reticular nucleus of rat medulla oblongata, suggesting that PAs are one of the components of biologically active ribosome, being closely involved in the translation processes of protein biosynthesis.
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Immunocytochemical Localization of Histamine in Enterochromaffin-like (ECL) Cells in Rat Oxyntic Mucosa: A Transmission Electron Microscopy Study Using Monoclonal Antibodies and Conventional…

It is suggested that in ECL cells HA is enzymatically synthesized in the cytoplasm, then is transported and stored in the cores of the granules before its release from the basal lamina.
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Determination of urinary acetylpolyamines by a monoclonal antibody-based enzyme-linked immunosorbent assay (ELISA).

The ASPM-2 ELISA for N1-Ac-Spd, which is the PA most relevant to the analysis of human urine among the three Ac-PAs mentioned above, is specific and accurate, and can easily be used to analyze large numbers of specimens in parallel.
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Development and application of a sandwich enzyme immunoassay for Glycyrrhizae Radix protein (GRP) using monoclonal antibodies.

The present SEIA was about 10-times more sensitive in detecting GRP than the selected antibody enzyme immunoassay for GRP previously developed using an antiserum to GR itself, and may provide a general analytical method for the quality control of GR-based TCMs.
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A general enzyme immunoassay for the licorice root component contained in traditional Chinese medicines.

The SAEIA was successful in the detection and quantitative measurement of GR component contents in Chinese traditional medicines and the technique of selected antibody enzyme immunoassay (SAEIA) was applied to develop a sensitive general assay method.
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Enzyme immunoassay for a characteristic protein in the animal crude drug lumbricus.

The SAEIA for 70 kDa protein was simple, accurate, reproducible and may provide a general analytical method for the quality control of Lumbricus-based TCMs.
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