Radioisotope labelling

Labeling. Radioisotopic labeling, one of the first labeling methods used, is stiU prominent in assays where the use of nonradioisotopic labels... 

Immunochemical metliods drat utilize radioisotopic labeling can detect tire use of anabolic sex hormones drat increase die growdi in meat animals. Stilbene [588-59-0] trenbolone [10161 -33-8] and zeranol [55331-29-8] C gH2 0, can be successfully monitored by diese immunoassay techniques... 

Definitive identification of lysine as the modified active-site residue has come from radioisotope-labeling studies. NaBH4 reduction of the aldolase Schiff base intermediate formed from C-labeled dihydroxyacetone-P yields an enzyme covalently labeled with C. Acid hydrolysis of the inactivated enzyme liberates a novel C-labeled amino acid, N -dihydroxypropyl-L-lysine. This is the product anticipated from reduction of the Schiff base formed between a lysine residue and the C-labeled dihydroxy-acetone-P. (The phosphate group is lost during acid hydrolysis of the inactivated enzyme.) The use of C labeling in a case such as this facilitates the separation and identification of the telltale amino acid. 

Radioisotope-labeled nitrosamines have proven valuable in development of analytical methods and for demonstrating efficiency of recovery of nitrosamines from tobacco products and smoke (37-39). The very high specific activity required for low part-per-billion determinations has discouraged most analysts from using this approach. Unless a radiochromatographic detector with adequate sensitivity is available, samples must be counted independently of the final chromatographic determination, and one of the advantages of internal standardization, correction for variation in volume injected, is lost. 

In this work the methanol and methyl iodide conversion and their co-reaction are investigated on Fe-Beta zeolite without any oxygen. Partly Fe-ion-exchanged Beta-300 i.e. Fe-H-Beta-300 (shortly Fe-Beta-300) zeolite keeps the light acidity to a certain extent, however the presence of Fe ions (as transition metal, Fe is an excellent Lewis acid) can modify the reaction pathway. This Fe-Beta-300 has been tested already by low temperature peat pyrolysis [6], At present, the adsorption as well as desorption of methanol are followed-up by radiodetectors using ( -radioisotopic labeling [4, 7]. The... 

When cells are suspended in a biological fluid or culture medium, both serum proteins and cells interact with the surface substrate. Serum protein adsorption behavior on SAMs has been examined with various analytical methods, including SPR [58-61], ellipsometry [13, 62, 63], and quartz QCM [64—66]. These methods allow in situ, highly sensitive detection of protein adsorption without any fluorescence or radioisotope labeling. SPR and QCM are compatible with SAMs that comprise alkanethiols. In our laboratory, we employed SPR to monitor protein adsorption on SAMs. 

For many years, due to the availability and low cost of radioisotope-labeled secondary antibodies, radioactive detection was the method of choice in Western blotting. Newer methods that are less hazardous and easier to use, while maintaining comparable sensitivity, have been developed. Today, Western blotting detection methods can be light-based, (chemiluminescence, bioluminescence, chemifluorescence, and fluorescence), radioactivity-based, or color-based. It is important to note that the detection sensitivity depends on the affinity of the primary antibody for the antigen and on the affinity of the secondary antibody for the primary antibody and can therefore vary considerably from one protein sample to another and from one antibody batch to another. 

A radiometric technique for estimating the rates of intracellular synthesis and/or turnover of a metabolite. To measure the rates of synthesis, cells are exposed to a radioisotopically labeled precursor (such as pH]-,... 

Much research has gone into raising the sensitivity and selectivity of immunosensors to the desired levels. Several labels have proved to ensure a high sensitivity, yet radioisotopic labels have essentially been avoided. Non-isotopic labels for immunosensors include various enzymes, catalysts, fluorophores, electrochemically active molecules and liposomes. Labelled immunosensors are basically designed so that immunochemical complexation takes place on the surface of the sensor matrix. There are several variants of the procedure used to form an immunocomplex on the matrix. In the final step, however, the label should always be incorporated into the immunocomplex for determination, as shown in Fig. 3.27.B. 

N.J. Baldwin, Y. Wang, T.C. Ng, In situ F MRS measurement of RIF-1 tumor blood volume Corroboration by radioisotope-labeled [ l]-albumin and correlation to tumor size, Magn. Reson. Imaging 14 (1996) 275-280. 

Immunochemical methods that utilize radioisotopic labeling can detect the use of anabolic sex hormones that increase the growth in meat animals. Stilbene [588-59-0], C14H12, trenbolone [10161-33-8], and zeranol [55331-29-8], C18H2605, can be successfully monitored by these immunoassay techniques (45). In order to prevent veterinary dmgs from being transported to the human food chain, radioisotopic immunoassays were developed to monitor veterinary antibiotics such as penicillin and chloramphenicol [56-75-7], C H CyX C, in meat, milk, and eggs (qv) (see Antibiotics Meat products Milk AND MILKPRODUCTS). 

For the membrane array of cytokine expression, the general procedures (Amersham Pharmacia Biotech R D Systems SuperArray Inc., Bethesda, MD Clontech Laboratories, Inc., Palo Alto, CA) include RNA extraction, reverse transcription into biotin- or radioisotope-labeled cDNA, hybridization with about 20 to several hundred different cDNA prespotted membranes, and signal detection using fluorescence or radioactive methods (L3). As an example, Fig. 4 and Table 4 show different chemokine genes upregulated in allergic asthmatic patients compared with normal controls, based on membrane array technology (SuperArray). 

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