Download - Primary culture ch:12
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Primary culture ch:12
By : Saib al owini
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Primary culture: steps
• 1- ISOLATION OF THE TISSUE• 2- Dissection and/or disaggregation : - Mechanically: sieving or pipetting - or chemically : crude or pure enzymes (trypsin alone or trypsin/EDTA ) , (glycanases, such
as hyaluronidase or heparinase,), (collagenase, dispase, pronase )
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• Trypsin + pronase : complete but may damage • Collagenase + dispase : incomplete ,safe • Hyaluronidase + collagenase : for matrix
digestion • DNASE : for released DNA and support
reaggregation • 3- Culture
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General requirements for 1ry culture
• Remove necrotic and lipids• Sharp instrument • Enzymes must removed • Begin with large # not all will survive • F12/DMEM with serum as beginning• Embryonic tissue is preferable ( soft,
proliferation rate)
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ISOLATION OF THE TISSUE
• Ethical processes • Sterility • Bss • Where to dissect
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Mouse Embryo
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Protocol
• Induction of estrus• Dating the embryos• Kill the mouse by cervical dislocation• Tear the ventral skin transversely at
themedian line• Dissect out the uteri into a 25-mL or 50-mLscrew-capped vial containing 10 or 20 mL DBSS
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Human biopsy
• Problems:-Many consents -Patent rights - The operation is performed by physicians - You will receive and record but it may has a
risk infection
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PROTOCOL
Decontamination. Although most surgical speci-mens are sterile when removed,
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PRIMARY EXPLANT
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FINE CHOPED
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3 DAY 7 DAY
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Warm Trypsin
Enzymatic Disaggregation
EDTA or EGTAEGTA (ethylene glycol tetraacetic acid)(ethylenediaminetetraacetic acid )
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Trypsinization with Cold Preexposure
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SEPARATION OF VIABLE CELLS