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Titlebook: Analytical Morphology; Theory, Applications Jiang Gu Book 1996 Springer Science+Business Media New York 1996 biology.cell.chemistry.develop

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期刊全称Analytical Morphology
期刊简称Theory, Applications
影响因子2023Jiang Gu
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图书封面Titlebook: Analytical Morphology; Theory, Applications Jiang Gu Book 1996 Springer Science+Business Media New York 1996 biology.cell.chemistry.develop
Pindex Book 1996
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Elimination of Background Staining in Immunocytochemistry,. Once the cause is identified, measures can be taken to rectify the problem. One of the limitations of the widely employed indirect immunocytochemistry technique is that rabbit polyclonal antibodies cannot be used on rabbit tissue because of the strong, obscuring background that usually occurs. We
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Principles, Applications and Protocols of Microwave Technology for Morphological Analysis,anded considerably beyond their initial use as a safe, clean and rapid method of tissue fixation. Microwaves can now be employed for the fixation of large specimens, including brain, to accelerate the action of cross-linking fixatives, as well as to greatly reduce the various stages of tissue proces
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Microwave Immunohistochemistry: Advances in Temperature Control, were tested. The probe was designed to be submerged in a drop of immunoreagent on a glass slide, and the measured temperature of the droplet was used to regulate the output power and the time needed for the magnetron to reach and maintain the desired incubation temperature. A three-step streptavidi
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Applications of , Hybridization and Immunocytochemistry for Localization and Quantification of Peptlls generally express several neurohormonal peptide messengers—sometimes together with non-peptide messengers—and this expression may be subject to alterations during ontogeny and under pathological conditions. In addition, the level of messenger expression is regulated in response to physiological
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An Optimized Protocol for , Hybridization Using PCR-Generated ,P-Labeled Riboprobes, of probe constructs and tissue types. Specific advances incorporated into this protocol include (1) the use of PCR gene fragments to generate cRNA probes, (2) the use of .P-labeled probes and (3) the use of ultrafiltration microconcentrators to purify the probe and eliminate background. The use of
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