Titlebook: Systolic Time Intervals; International Sympos Werner List,Joachim S. Gravenstein,David H. Spodic Conference proceedings 1980 Springer-Verla

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J. Simonyi,J. Lehoczky,Z. Herpai,A. Godry,I. Szauderks.Contains expert notes and vital implementation advice.Inc.Unlike detecting constitutively expressed targets, immunohistochemical detection of labile, low abundance, and short-lived signal transduction molecules can be a very difficult task.  In .Signal Transduction Immunohistochemistry: Methods a

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J. Zanella Jr.,R. Steinberg,P. Katona,P. J. Dauchot,J. S. Gravensteinks.Contains expert notes and vital implementation advice.Inc.Unlike detecting constitutively expressed targets, immunohistochemical detection of labile, low abundance, and short-lived signal transduction molecules can be a very difficult task.  In .Signal Transduction Immunohistochemistry: Methods a

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H. Mannebach,L. Bechtloff,H. H. Mertens,L. Przybilla,U. Gleichmannks.Contains expert notes and vital implementation advice.Inc.Unlike detecting constitutively expressed targets, immunohistochemical detection of labile, low abundance, and short-lived signal transduction molecules can be a very difficult task.  In .Signal Transduction Immunohistochemistry: Methods a

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G. Ferro,M. Chiarello,V. Santinelli,M. G. Tari,M. Condorelliles can be a very difficult task.  In .Signal Transduction Immunohistochemistry: Methods and Protocols., IHC experts contribute detailed protocols addressing the numerous challenges of signal-transduction immunohistochemistry (ST-IHC).  Beginning with a set of introductory chapters, the volume moves

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W. Rentschationships between proteins with cellular resolution. Detections are performed simultaneously or sequentially depending on the approach. However, several technologies can detect limited numbers of antigens or require expensive equipment and reagents. Another serious concern is the lack of flexibilit

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G. K. Wolfaped structure with two folded domains, which are connected by a flexible linker in solution. The calmodulin-binding domains of the target proteins are contained in 20 residue long amino acid sequences, that share no obvious amino acid sequence homology. In this contribution, we discuss the features