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细胞功能测定

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Preparation of Colloidal Gold Particles and Conjugation to Protein A, IgG, F(ab)2, and Streptavidin

Colloidal gold probes, including protein A-, IgG-F(ab’)2-, and streptavidin-labeled gold particles, are useful tools for localization of antigens in cells and tissues by immunoelectron microscopy (IEM). This chapter describes different methods for the preparation of colloidal g ...

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Production of Antipeptide Antibodies

Peptides (8–20 residues) are as effective as proteins in raising antibodies, both polyclonal and monoclonal with a titer above 20,000 easily achievable. A successful antipeptide antibody production depends on several factors such as peptide sequence selection, peptide synthesi ...

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Pre-embedding Immunoelectron Microscopy of Chemically Fixed Mammalian Tissue Culture Cells

Immunoelectron microscopy is one of the best methods for detecting and localizing protein molecules in cells and tissues. Gold particles of 1.4nm in diameter (Nanogold) conjugated with Fab’ fragments easily penetrate into the cell interior and are used for pre-embedding immunoelect ...

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Immunoelectron Microscopy of Cryofixed and Freeze-Substituted Plant Tissues

Cryofixation and freeze-substitution techniques preserve plant ultrastructure much better than conventional chemical fixation techniques. The advantage of cryofixation is not only in structural preservation, as seen in the smooth plasma membrane, but also in the speed in arre ...

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In Vivo Cryotechniques for Preparation of Animal Tissues for Immunoelectron Microscopy

The final goal of immunohistochemical studies is that all findings examined in animal experiments should reflect the physiologically functional background. Therefore, the preservation of original components in cells and tissues is necessary for describing the functional mo ...

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Immunoelectron Microscopy of Cryofixed Freeze-Substituted Mammalian Tissue Culture Cells

Mammalian tissue cultured cells are widely used in cell biology research. Immunoelectron microscopy is a powerful technique to define the subcellular localization of targeted antigens in the cultured cells. Cryofixation is now generally accepted as the best initial fixation step, ...

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Immunoelectron Microscopy of Cryofixed Freeze-Substituted Saccharomyces cerevisiae

Immunolabelling electron microscopy is a challenging technique with demands for perfect ultrastructural and antigen preservation. High-pressure freezing offers an ideal way to fix cellular structure. However, its use for immunolabelling has remained limited because of the l ...

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High-Resolution Molecular Localization by Freeze-Fracture Replica Labeling

The freeze-fracture technique splits the frozen lipid bilayer membrane into two halves and immobilizes membrane proteins and lipids by the vacuum evaporation of platinum and carbon. After a treatment by SDS to remove extramembrane materials, the specimen is subjected to immunogold l ...

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Pre-embedding Electron Microscopy Methods for Glycan Localization in Chemically Fixed Mammalian Tissue Using Horseradish Peroxidase-Conjugated Lectin

In histochemistry and cytochemistry, horseradish peroxidase-labeled lectins are often used as probes for the localization of carbohydrates in cells and tissues. In transmission electron microscopy, the most commonly used procedure for detection of carbohydrates is lectin– ...

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The Post-embedding Method for Immunoelectron Microscopy of Mammalian Tissues: A Standardized Procedure Based on Heat-Induced Antigen Retrieval

We describe a standardized method of fixation, antigen retrieval, and image contrasting for post-embedding immunoelectron microscopy. Tissues are fixed with formaldehyde solutions containing Ca2+ and Mg2+ ions at pH 7.4 and then at pH 8.5. After dehydration with dimethylformamide, t ...

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Pre-embedding Nanogold Silver and Gold Intensification

Pre-embedding nanogold silver and gold intensification methods involve immunoreactions with nanogold-labeled antibodies and intensification of the nanogold particles before embedding and ultrathin sectioning. These highly sensitive methods show good resolution ...

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Double-Label Immunoelectron Microscopy for Studying the Colocalization of Proteins in Cultured Cells

Multiple label immunoelectron microscopy localizes and detects multiple antigens in cells and tissues. In double labeling, two kinds of primary antibodies from different animal species are used after being mixed in a single solution. To distinguish the different antigens, seconda ...

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Methods to Analyze Subcellular Localization and Intracellular Trafficking of Claudin-16

The integral tight junction protein Claudin-16 (Cldn16) is predominantly expressed in renal epithelial cells of the thick ascending limb of Henle’s loop where, together with claudin-19, it forms a cation-selective pore that allows influx of Na+ from the interstitial fluid into the lumen of t ...

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Measuring Size-Dependent Permeability of the Tight Junction Using PEG Profiling

Tight junctions restrict the paracellular movement of ions, solutes, drugs, and larger material across epithelia and endothelia. For practical purposes, the barrier can be modeled as having two components. The first is a system of small 4  � radius pores lined or created by claudins. The pores show ...

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Identification of Claudins by Western Blot and Immunofluorescence in Different Cell Lines and Tissues

Claudins are integral proteins of the TJ. Each epithelia in the organism expresses a unique set of claudins that determines the degree of sealing of the paracellular pathway and the ionic selectivity of the tissue. TJs are dynamic structures whose organization and composition change in resp ...

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Expression and Function of Claudins in Hepatocytes

Tight junctions of hepatocytes play crucial roles in the barrier to keep bile in bile canaliculi away from the blood circulation, which we call the blood–biliary barrier. Tight junction proteins of hepatocytes are regulated by various cytokines and growth factors via distinct signal tra ...

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Analysis of Changes in the Expression Pattern of Claudins Using Salivary Acinar Cells in Primary Culture

Primary saliva is produced from blood plasma in the acini of salivary glands and is modified by ion adsorption and secretion as the saliva passes through the ducts. In rodents, acinar cells of salivary glands express claudin-3 but not claudin-4, whereas duct cells express both claudins-3 and -4. The ...

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Using Molecular Tracers to Assess the Integrity of the Intestinal Epithelial Barrier In Vivo

The examination of the epithelial barrier has been a primary site of focused research for years. Despite the importance of this site to numerous intestinal diseases, the determination of the integrity of this barrier has been clouded by controversies as to the validity of certain techniques a ...

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Development of Biological Tools to Study Claudins in the Male Reproductive Tract

It is estimated that between 12 and 15% of couples are infertile. More than half of these are related to problems associated with male reproductive dysfunction. Of those, 40% occur from idiopathic or unexplained causes. While spermatozoa are formed in the testis, testicular spermatozoa are im ...

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Laboratory Methods in the Study of Endometrial Claudin-4

Immunohistochemistry is a suitable method for the detection of proteins from the Claudin family and several antibodies are commercially available for the detection of Claudin congeners. Immunodetection of Caludin-4 in the paraffin-embedded specimens might be a useful tool for st ...

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