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	<title>Epi293 Protein Production - Revision history</title>
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	<updated>2026-10-18T06:19:16Z</updated>
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		<id>https://eln.excellgen.com/index.php?title=Epi293_Protein_Production&amp;diff=6280&amp;oldid=prev</id>
		<title>Paul.xu: Created page with &quot;== Transfection and Expression ==  &lt;br&gt;Follow the procedure below to transfect suspension Expi293F Cells in a 30 mL volume. For each 30 mL transfection, you will need 7.5 × 107 ...&quot;</title>
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		<updated>2012-10-01T01:38:47Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;== Transfection and Expression ==  &amp;lt;br&amp;gt;Follow the procedure below to transfect suspension Expi293F Cells in a 30 mL volume. For each 30 mL transfection, you will need 7.5 × 107 ...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;== Transfection and Expression ==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;br&amp;gt;Follow the procedure below to transfect suspension Expi293F Cells in a 30 mL volume. For each 30 mL transfection, you will need 7.5 × 107 cells in 25.5 mL of Expi293 Expression Medium.&lt;br /&gt;
&lt;br /&gt;
&amp;lt;br&amp;gt;1. The day before transfection (day –1), seed Expi293F Cells at a density of 2.0 × 10^6 viable cells/mL in Expi293 Expression Medium to transfect them on the following day (day 0).&lt;br /&gt;
&lt;br /&gt;
2. Incubate the cells overnight in a 37°C incubator with a humidified atmosphere of 8% CO2 in air on an orbital shaker rotating at 125 rpm.&lt;br /&gt;
&lt;br /&gt;
3. On the day of transfection (day 0), determine cell viability using an automated cell counter or the trypan blue dye exclusion method.&amp;lt;br&amp;gt;Important: Cell should not be clumping and viability of cells must be over 95% to proceed with transfection.&lt;br /&gt;
&lt;br /&gt;
4. Add the appropriate volume of cell suspension containing 7.5 × 10^7 cells (see Note on page 1) into a sterile, disposable 125-mL Erlenmeyer shaker flask, and bring up the volume to 25.5 mL with fresh, pre-warmed Expi293 Expression Medium. Return the cells to the incubator.&lt;br /&gt;
&lt;br /&gt;
5. Prepare lipid-DNA complexes by performing the following:&lt;br /&gt;
&lt;br /&gt;
a. Dilute 30 μg (i.e., 30 μL) of Antibody Expressing Positive Control Vector in Opti-MEM® I medium to a total volume of 1.5 mL. Mix gently.&lt;br /&gt;
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b. Dilute 80 μL of ExpiFectamine 293 Reagent in Opti-MEM I medium to a total volume of 1.5 mL. Mix gently and incubate for 5 minutes at room temperature.&amp;lt;br&amp;gt;Note: Longer incubation times may result in decreased activity.&lt;br /&gt;
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c. After the 5 minutes, add the diluted control vector DNA to the diluted ExpiFectamine 293 Reagent to obtain a total volume of 3 mL. Mix&amp;lt;br&amp;gt;gently.&lt;br /&gt;
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d. Incubate DNA-ExpiFectamine 293 Reagent mixture for 20–30 minutes at room temperature to allow the DNA-ExpiFectamine 293 Reagent complexes to form.&lt;br /&gt;
&lt;br /&gt;
6. After the DNA-ExpiFectamine 293 Reagent complex incubation is complete, add the DNA-ExpiFectamine 293 Reagent complex to the cells from Step 4. The flask should contain a total volume of 28.5 mL.&lt;br /&gt;
&lt;br /&gt;
7. Incubate the cells in a 37°C incubator with a humidified atmosphere of 8% CO2 in air on an orbital shaker rotating at 125 rpm.&lt;br /&gt;
&lt;br /&gt;
8. Approximately 16–18 hours post-transfection, add 150 μL of ExpiFectamine 293 Transfection Enhancer 1 and 1.5 mL of ExpiFectamine 293 Transfection Enhancer 2 to each flask. The final volume should be approximately 30 mL in each 125-mL flask.&lt;br /&gt;
&lt;br /&gt;
9. The rabbit IgG expressed by the control will be secreted into the Expi293 Expression Medium. Expression can be detected by day 3 post-transfection;&amp;lt;br&amp;gt;however maximum yield is obtained 6–7 days post-transfection. The expected yield of the control IgG is approximately 200–300 mg IgG per liter of culture on day 7.&amp;lt;br&amp;gt;&amp;lt;br&amp;gt;&lt;br /&gt;
&lt;br /&gt;
[[Category:Protocols]]&lt;/div&gt;</summary>
		<author><name>Paul.xu</name></author>
	</entry>
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