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        丁香实验推荐阅读
        Detection of t(14; 18)(q32;q21)-Associated BCL-2/JH Gene Fusion in Non-Hodgkin Lymphoma

        The identification and study of nonrandom recurrent chromosomal translocations has substantially increased our understanding of the non-Hodgkin lymphomas. Cytogenetic and molecular genetic data now form an integral part of current lymphoma classifications (1) and provi ...

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        RNA Extraction from Fresh or Frozen Tissues

        RNA can be isolated from fresh or frozen tissue, then purified and quantified for subsequent molecular analysis. RNA is quite labile compared to DNA for good reason: RNA is the transient message that transmits information from activated genes. Once gene transcription is turned off, no more RNA is ...

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        Single-Strand Conformation Polymorphism Analysis of Mutations in Exons 4-8 of the TP53 Gene

        The TP53 tumor suppressor gene coding for a nuclear phosphoprotein involved in cellular stress responses is the most frequently mutated gene in human cancers described so far (1–4). Mutations are found throughout the gene but most frequently within the highly conserved middle region (ex ...

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        Detection of Telomerase by In Situ Hybridization and by the Polymerase Chain Reaction-Based Telomerase Activity Assay

        The onset of human cancer typically requires numerous genetic mutations, generally specific for the tissue type from which the cancer originates. Thus, it has been difficult to screen all tumor types for a single mutation. In recent years, telomerase activity has been associated with at least ...

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        Detection of Microsatellite Instability

        In 1993, three groups independently discovered that the lengths of microsatellites in tumors could vary from the normally constant pattern defined at birth (5–5) (see review in ref. 4). This discovery has been designated either microsatellite instability (MSI) or replication errors (R ...

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        Polymerase Chain Reaction Clonality Assays Based on X-Linked Genes

        During embryogenesis in females, in each cell either the paternal or the maternal X chromosome is randomly inactivated through methylation (1 2). This event is stably inherited by daughter progeny of each cell. Therefore, in adult women, polyclonal cell populations will comprise a random mi ...

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        Fluorescent In Situ Hybridization: Evaluation for Ploidy and Gene Amplification

        In situ hybridization was first described in the late 1960s by Pardue and Gall (1), who hybridized mouse ribosomal DNA sequences to a mouse chromosome spread. The technique came into broader use with the description of DNA probes for various viral sequences, and in the late 1980s with the publicatio ...

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        Conformation as Therapeutic Target in the Prionoses and Other Neurodegenerative Conditions

        Neurodegenerative conditions are increasing in prevalence as the average human life expectancy rises. Alzheimer’s disease (AD) is the fourth commonest cause of death in the United States; the recent outbreak of new variant Creutzfeldt-Jakob disease (nvCJD) has raised the specter of a la ...

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        Transmissible Spongiform Encephalopathy Neurobiology and Ultrastructure Suggests Extracellular PrPSc Conversion Consistent with Classical Amyloidosis

        The infectious cause of the transmissible spongiform encephalopathies (TSEs), or prion diseases, is not yet clearly defined. Although minorities of researchers cling tenaciously to the virus hypothesis, the prion or protein-only hypothesis is now widely accepted by most scientis ...

        丁香实验推荐阅读
        Prions of Yeast From Cytoplasmic Genes to Heritable Amyloidosis

        It was believed that only proteins could carry out enzymatic reactions, and only nucleic acids could mediate inheritance. In recent years, the work of Cech and Altman and others has shown that nucleic acids can catalyze reactions. Now it has been shown that, in yeast, proteins can mediate inheritan ...

        丁香实验推荐阅读
        What Would Thomas Henry Huxley Have Made of Prion Diseases

        “Science is nothing but trained and organized common sense, differing from the latter only as a veteran may differ from a raw recruit.”a Prion disease is a disease of the second half of the twentieth century, but the scientific method that has elucidated this fascinating group of diseases is much olde ...

        丁香实验推荐阅读
        Prion Protein as Copper-Binding Protein at the Synapse

        Various approaches have been taken to study the function of prion proteins. Biochemical methods were applied to search for a binding partner of PrPC which is attached to the cell surface by a glycosylphosphatidylinositol GPI anchor (1). The glial fibrillary acidic protein was one of the first p ...

        丁香实验推荐阅读
        A Function for the Prion Protein

        Protein function is often observed directly following protein isolation, or is deduced by loss of function following gene knockout or by analogy with proteins of known function and similar amino acid sequence. None of these is true in the case of prion proteins because aside from the association ...

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        Prion Protein Peptide: Agents of Death for Neurons

        The fundamental problem in addressing prion diseases, or the transmissible spongiform encephalopathies, is finding an explanation for the massive neuronal death that occurs. Although some understanding of the mechanism by which neuronal death occurs comes from studies with scr ...

        丁香实验推荐阅读
        Characterization of Bovine Spongiform Encephalopathy and Scrapie Strains/Isolates by Immunochemical Analysis of PrPSc

        In the past two decades, thoroughly standardized mouse incubation time and brain lesion profile scoring assays have been developed to discriminate between prion strains. However, in these mouse infection experiments, large numbers of animals (about 20 mice/line) from three differe ...

        丁香实验推荐阅读
        Differential Targeting of Neurons by Prion Strains

        A basic principle of microbiology that applies to all conventional infectious pathogens is that the disease phenotype is a function of both the infecting agent and the host’s response to it. All evidence indicates that this principle is also true for diseases acquired by infection with prions, ...

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        Prions: From Neurografts to Neuroinvasion

        The prion hypothesis states that the partially protease-resistant and detergent-insoluble prion protein (PrPSc) is identical with the infectious agent, and lacks any detectable nucleic acids. Since the latter discovery, transgenic mice have contributed many important insig ...

        丁香实验推荐阅读
        Transgenic Studies of Prion Diseases

        This chapter reviews studies that involve the manipulation of prion protein (PrP) genes by transgenesis in mice. These consist of two approaches: PrP gene knockout and gene replacement using homologous recombination in embryonic stem cells; and microinjection of transgenes into fer ...

        丁香实验推荐阅读
        Cellular and Transgenic Models of Familial Prion Diseases

        Prion diseases are fatal neurodegenerative disorders of humans and animals, which result from the conformational conversion of a normal, cell surface glycoprotein (PrPC) into a pathogenic isoform (PrPSc) that is the main component of infectious prions (1,2) . Familial prion diseases, ...

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        Analysis of Protein Expression in Muscular Dystrophies

        The preceding chapters have dealt with the detection of gene mutations and the following chapters deal with protein analysis. This chapter links the two by describing the effect that different types of mutations have on protein synthesis, and how this may be used in the investigation of muscular ...

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