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        丁香实验推荐阅读
        Alkaline Phosphatase for Glycol Methacrylate Sections

        Alkaline Phosphatase for Glycol Methacrylate SectionsProcedure:Incubate sections in the incubating medium at room temperature for 1 - 3 hours. Two hours is sufficient in most cases. Wash in distilled ...

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        Glycol Methacrylate Embedding for Immunohistochemistry

        Glycol Methacrylate Embedding for ImmunohistochemistryTechnovit Glycol Methacrylate: Technical Information and Help From Heraeus Kulzer.Embedding in plastic provides many advantages to the histotechno ...

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        Glycol Methacylate Embedding for Materials Samples

        Glycol Methacylate Embedding for Materials SamplesTechnovit Glycol Methacrylate: Technical Information and Help From Heraeus Kulzer.Embedding in a plastic often supplies the support necessary to succe ...

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        Staining Protocols for Lymphoid Tissue:

        Staining Protocols for Lymphoid Tissue:Technovit Glycol Methacrylate: Technical Information and Help From Heraeus Kulzer.Normal immunostaining procedures for routine markers on sections obtained from ...

        丁香实验推荐阅读
        COMBINED ALCIAN BLUE - P.A.S

        COMBINED ALCIAN BLUE - P.A.S SECTIONS4micron paraffin wax sectionsSOLUTIONS1. Alcian Blue pH 2.5Alcian Blue 1g3% Acetic Acid 100ml2. 1% Periodic Acid 3. Schiffs ReagentMETHODTake sections to waterPlac ...

        丁香实验推荐阅读
        Periodic Acid Schiff Stain for Glycol Methacrylate Sections

        Periodic Acid Schiff Stain for Glycol Methacrylate Sections Technovit Glycol Methacrylate: Technical Information and Help From Heraeus Kulzer.Procedure: Oxidize sections in 0.4% periodic acid for 30 m ...

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        Sectioning and Mounting Protocol

        Sectioning and Mounting ProtocolTechnovit Glycol Methacrylate: Technical Information and Help From Heraeus Kulzer. SectioningSectioning is best done with a rotary or sledge microtome such as the JB-4 ...

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        for the technique of embedding specimens in plastic

        for the technique of embedding specimens in plasticDay 1Step 1: Read and understand the Material Safety Data Sheets associated with each of the chemicals used in this procedure. Use of rubber gloves l ...

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        Microwave citrate Pretreatment of Paraffin Sections

        1.Deparaffinize slides a (after drying thoroughly overnight at RT) in 2 changes of xylene (or xylene substitute) for 10 mins each. 2.Transfer slides to 100% alcohol 2 changes for at least 2 m ...

        丁香实验推荐阅读
        Preparation and Staining of Paraffin Sections

        Preparation and Staining of Paraffin Sectionsfor use with Pharmingen reagents I. Fixation and Processing of Tissue for Paraffin SectionsA. Fixation of Tissues in 10% Neutral Buffered FormalinSacrifice ...

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        Preparation and Staining of Frozen Tissue Sections

        Preparation and Staining of Frozen Tissue Sectionsfor use with Pharmingen reagents I. Preparation of Frozen Sections for SectioningMaterials neeed:2-methylbutane (isopentane) Liquid Nitrogen Dry ice P ...

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        SECTION ADHESIVES

        SECTION ADHESIVES It is advisable to use an adhesive to promote tissue attachment to the glass slides used in histological preparation. This is routinely achieved by the application of a smear of glyc ...

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        Tissue sectioning: Cryostat sectioning method

        Material MEMPfa: 0.1M MOPS -- pH 7.4 2mM EGTA 1mM MgSO4 (typically this is made up as 10X MSalts. 4% paraformaldehyde (diluted from a frozen stock of 20%) (store MEMPfa at 4C and use within 1 day). ...

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        Cryosectioning

        CryosectioningWhile the timing of the various steps in this protocol are probably not critical I tend to prefer to process the tissue all at once to ensure that RNA and/or proteins do not get degrade ...

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        FREEZING TISSUE FOR CRYOSTAT SECTIONING

        All tissue types except muscle:Tissue should preferably be snap-frozen by quenching in liquid nitrogen. Quenching is accomplished by putting a small amount of OCT compound onto a cork disc placing the ...

        丁香实验推荐阅读
        FREEZING TISSUE FOR CRYOSTAT SECTIONING

        All tissue types except muscle:Tissue should preferably be snap-frozen by quenching in liquid nitrogen. Quenching is accomplished by putting a small amount of OCT compound onto a cork disc placing the ...

        丁香实验推荐阅读
        Hematoxylin Stain

        Hematoxylin StainSolutionsHematoxylinHematoxylin6.4gAmmonium alum60gEthanol200mlGlycerol160mlDistilled water640mlMix for a day then allow the solution to ripen in the dark for at least a month before ...

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        ACETYL CHOLINESTERASE

        ACETYL CHOLINESTERASE SECTIONS Unfixed cryostat or cold Formol calcium/gum sucrose fixed sections. SOLUTIONS a. Incubating solution. --acetyl thiocholine iodide 5mg --0.1M acetate buffer (pH.6.0) 6.5m ...

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        ACID PHOSPHATASE

        ACID PHOSPHATASE Sections 5-10 micron unfixed or cold formol calcium/gum sucrose fixed Cryostat sections.Stock solutionsA) Pararosanilin-HCL StockPararosanilin 1gDistilled water 20mlHCl Conc 5mlThe pa ...

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        Stain for Sperm Acrosomes

        Stain for Sperm Acrosomes Procedure 1. After sperm preparation adjust sperm concentration as high as possible (5-10 x 106/ml). 2. Prepare a smear of sperm suspention onto a slide and allow it to dry. ...

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