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	<title>Cell Adaptation Protocol - Revision history</title>
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	<updated>2026-10-18T03:03:34Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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		<id>https://eln.excellgen.com/index.php?title=Cell_Adaptation_Protocol&amp;diff=11289&amp;oldid=prev</id>
		<title>Paul.xu: Created page with &quot;= Cell Adaptation Protocols&lt;br&gt; =  == Introduction ==  There are two approaches to be considered when adapting cells to Sf-900 II SFM: 1) Direct planting of cells from medium con...&quot;</title>
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		<updated>2014-02-20T22:33:29Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;= Cell Adaptation Protocols&amp;lt;br&amp;gt; =  == Introduction ==  There are two approaches to be considered when adapting cells to Sf-900 II SFM: 1) Direct planting of cells from medium con...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;= Cell Adaptation Protocols&amp;lt;br&amp;gt; =&lt;br /&gt;
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== Introduction ==&lt;br /&gt;
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There are two approaches to be considered when adapting cells to Sf-900 II SFM: 1) Direct planting of cells from medium containing serum to Sf-900 II SFM; 2) Sequential adaptation or “weaning&amp;quot;. It is critical that cell viability be at least 90% and the growth rate be in mid-logarithmic phase prior to initiating adaption procedures.&lt;br /&gt;
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== Materials and Equipment: ==&lt;br /&gt;
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Incubator capable of maintaining 28°C ± 0.5°C, and large enough to accommodate orbital shaker with dual platform.&lt;br /&gt;
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Insect cell culture growth medium: Sf-900 II SFM and currently used complete medium.&lt;br /&gt;
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Microscope, Hemocytometer&lt;br /&gt;
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Electronic Cell Counter&lt;br /&gt;
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Low speed centrifuge&lt;br /&gt;
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Pipettes: 1 mL, 5 mL, 10 mL, 25 mL&lt;br /&gt;
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Pasteur pipettes&lt;br /&gt;
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250 mL sterile disposable Erlenmeyer flasks&lt;br /&gt;
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== A. Direct Adaptation ==&lt;br /&gt;
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1) Cells growing in 5% to 10% FBS supplemented medium are transferred directly into prewarmed Sf-900 II SFM following parameters set in III, steps 1-10.&lt;br /&gt;
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2) When the cell density reaches 1-3 x 10 6th&lt;br /&gt;
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cells/mL (4-6 days post planting), subculture to a density of 3 x 10 5th cells/mL.&lt;br /&gt;
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3) When the cells are completely adapted to serum-free culture they will reach a density in excess of 4 x 10 6th&lt;br /&gt;
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viable cells/mL after approximately 7 days culture.&lt;br /&gt;
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4) Stock cultures of SFM adapted cells should be subcultured twice weekly when the viable cell count&lt;br /&gt;
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reaches 1 to 3 x 10 6th cells/mL with at least a 90% viability.&lt;br /&gt;
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Note: If suboptimal performance is achieved using the direct adaptation method, use the sequential adaptation (weaning) method.&lt;br /&gt;
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== B. Sequential Adaptation / Weaning Procedure ==&lt;br /&gt;
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1) Subculture Sf9 cells grown in conventional medium with 5-10% serum into a 50:50 ratio of Sf-900 II SFM and the original serum supplemented media.&lt;br /&gt;
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2) Incubate according to III, steps 1-10 until viable cell count exceeds 6 x 10 5th cells/mL.&lt;br /&gt;
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Subculture by mixing equal volumes of culture and fresh Sf-900 II SFM.&lt;br /&gt;
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3) Continue to subdivide the culture in this manner until the calculated serum complement falls&lt;br /&gt;
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below 0.1%, cell viability is approximately 85% and a viable count in excess of 6 x 10 5th cells/mL is achieved.&lt;br /&gt;
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4) Subculture when the viable cell count reaches 1-2 x 10 6th cells/mL (approx. every 4-6 days post planting).&lt;br /&gt;
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5) After several passages the viable cell count should exceed 4 x 10 6th cells/mL with a viability exceeding 85% after approximately 7 days of culture. At this stage the culture is considered to be adapted to Sf-900 II SFM&lt;br /&gt;
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[[Category:Protocols]]&lt;/div&gt;</summary>
		<author><name>Paul.xu</name></author>
	</entry>
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