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	<title>Lentivirus-Production-CGMP - Revision history</title>
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	<updated>2026-10-18T14:09:26Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://eln.excellgen.com/index.php?title=Lentivirus-Production-CGMP&amp;diff=3414&amp;oldid=prev</id>
		<title>Paul.xu: Created page with &quot;=== 293T cells ===  1. Thaw a vial of 293T cells and place them in a Nunc T-75 flask.   2. Passage cells every three to four days into Nunc T-500 flasks  3. Transfer cells to 10-...&quot;</title>
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		<updated>2012-02-28T15:03:36Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;=== 293T cells ===  1. Thaw a vial of 293T cells and place them in a Nunc T-75 flask.   2. Passage cells every three to four days into Nunc T-500 flasks  3. Transfer cells to 10-...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;=== 293T cells ===&lt;br /&gt;
&lt;br /&gt;
1. Thaw a vial of 293T cells and place them in a Nunc T-75 flask. &lt;br /&gt;
&lt;br /&gt;
2. Passage cells every three to four days into Nunc T-500 flasks&lt;br /&gt;
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3. Transfer cells to 10-layer Nunc Cell Factory trays&lt;br /&gt;
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=== &amp;lt;br&amp;gt;Lentivirus production and Purification ===&lt;br /&gt;
&lt;br /&gt;
&amp;lt;br&amp;gt;1, Seed 1.25 × 10^5 cells/cm2 in 10-layer Corning CELLbind CellStack trays &amp;lt;br&amp;gt;or at 1 × 10^5cells/cm2 in T-75 flasks. &lt;br /&gt;
&lt;br /&gt;
2. Two days later, transfect cells with three helper plasmids (pCgp, pCMV-Rev2, and pCMV-G) and a lentiviral construct expressing target gene in a ratio of 20:13:5:20 respectively with 0.8 μg DNA/cm2. &lt;br /&gt;
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3. Remove transfection reagents (CaPO3) after a three-hour incubation&lt;br /&gt;
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4. Add fresh media containing 2% serum and 6 μM sodium butyrate. &lt;br /&gt;
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5. Harvest crude supernatant 72 hours later&lt;br /&gt;
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6. Add Benzonase nuclease at 50 U/mL in the presence of 2 mM Mg for six hours at 37 °C.&lt;br /&gt;
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7. Clarify culture supernatant by depth filtration using either a 0.45-μm capsule filter (Sartorius) or a 0.5-μm capsule filter (Millipore) with 3,000 cm2 of surface area. &lt;br /&gt;
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8. Use a hollow-fiber cartridge with a 500-kDa NMWC (GE Healthcare) to concentrate supernatant (from 10 L down to 2 L).&lt;br /&gt;
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9. diafilter viral supernatant to ~500 mL using 8 L chilled DF buffer (4 g/100 mL lactose from JT Baker in DPBS from MediaTech). &lt;br /&gt;
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10. Diafilter with an additional 2 L of DF buffer. &lt;br /&gt;
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11. Centrifuge viral suspension for 16–20 hours at 6,000g.&lt;br /&gt;
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12. Resuspend pellet and spin at 1,000 rpm for two minutes to pellet and remove insoluble material. &lt;br /&gt;
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13. Store viral vector at –80 °C &lt;br /&gt;
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14. p24 Titer Assay using HIV-1 p24 ELISA kit from PerkinElmer (catalog #NEK050).&lt;br /&gt;
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&amp;lt;br&amp;gt;&lt;br /&gt;
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[[Category:Lentivirus]][[Category:Protocols]]&lt;/div&gt;</summary>
		<author><name>Paul.xu</name></author>
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