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	<id>https://eln.excellgen.com/index.php?action=history&amp;feed=atom&amp;title=RBC_Lysing_Solutions</id>
	<title>RBC Lysing Solutions - Revision history</title>
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	<updated>2026-10-18T02:36:58Z</updated>
	<subtitle>Revision history for this page on the wiki</subtitle>
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	<entry>
		<id>https://eln.excellgen.com/index.php?title=RBC_Lysing_Solutions&amp;diff=15155&amp;oldid=prev</id>
		<title>Paul.xu: Created page with &quot;RBC Lysing Solutions and Cell Lysing Procedure  Ammonium chloride lyse (10X concentration)&lt;br/&gt;NH4Cl (ammonium chloride) 8.02gm&lt;br/&gt;NaHCO3 (sodium bicarbonate) 0.84gm&lt;br/&gt;EDTA...&quot;</title>
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		<updated>2016-07-31T01:44:30Z</updated>

		<summary type="html">&lt;p&gt;Created page with &amp;quot;RBC Lysing Solutions and Cell Lysing Procedure  Ammonium chloride lyse (10X concentration)&amp;lt;br/&amp;gt;NH4Cl (ammonium chloride) 8.02gm&amp;lt;br/&amp;gt;NaHCO3 (sodium bicarbonate) 0.84gm&amp;lt;br/&amp;gt;EDTA...&amp;quot;&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;RBC Lysing Solutions and Cell Lysing Procedure&lt;br /&gt;
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Ammonium chloride lyse (10X concentration)&amp;lt;br/&amp;gt;NH4Cl (ammonium chloride) 8.02gm&amp;lt;br/&amp;gt;NaHCO3 (sodium bicarbonate) 0.84gm&amp;lt;br/&amp;gt;EDTA (disodium) 0.37gm&amp;lt;br/&amp;gt;QS to 100ml with Millipore water. Store at 4 oC for six months.&lt;br /&gt;
&lt;br /&gt;
Working solution&amp;lt;br/&amp;gt;Dilute 10ml 10X concentrate with 90 ml Millipore water. Refrigerate until use.&amp;lt;br/&amp;gt;Procedure&amp;lt;br/&amp;gt;1.Obtain a whole blood specimen in a heparin tube.&amp;lt;br/&amp;gt;2.Aliquot 1ml blood into 15ml conical centrifuge tube.&amp;lt;br/&amp;gt;3.Fill tube to capacity with fresh cold lysing solution.&amp;lt;br/&amp;gt;4.Invert or rock for ~10 minutes at room temperature until liquid is clear red.&amp;lt;br/&amp;gt;5.Spin at 4C for 10 minutes at 250 x g.&amp;lt;br/&amp;gt;6.Decant supernatant and allow tubes to drain briefly.&amp;lt;br/&amp;gt;7.Resuspend cell by raking gently across a tube rack.&amp;lt;br/&amp;gt;8.Wash cells and combine multiple tubes with 10ml cold PBS/2% FCS.&amp;lt;br/&amp;gt;9.Spin, decant, and resuspend as above (steps 5-7).&amp;lt;br/&amp;gt;10. Count cells and adjust cell concentration to ~2-4x 106/ml.&lt;br /&gt;
&lt;br /&gt;
ERYTHROCYTE LYSING SOLUTION-10X STOCK SOLUTION (peripheral blood)Procedure&amp;lt;br/&amp;gt;1. Mix 14 ml 1x working solution (lysing buffer) to 1 ml Blood.&amp;lt;br/&amp;gt;2. Incubate for 3 - 5 minutes.&amp;lt;br/&amp;gt;3. Centrifuge at 300 x g for 5 minutes at room temperature.&amp;lt;br/&amp;gt;4. Aspirate supernatant and resuspend pellet in 5 ml of COLD Phosphate Buffered Saline(PBS).&amp;lt;br/&amp;gt;5. Centrifuge at 300 x g for 5 minutes at 2 - 8°C.&amp;lt;br/&amp;gt;6. Aspirate supernatant and resuspend pellet in 1 ml of COLD PBS with protein carrier&amp;lt;br/&amp;gt;10X Stock Lysing Buffer&amp;lt;br/&amp;gt;NH4Cl 89.9 g&amp;lt;br/&amp;gt;KHCO3 10.0 g&amp;lt;br/&amp;gt;Tetrasodium EDTA 370.0 mg&amp;lt;br/&amp;gt;Milli Q Water 1.0 Liter&amp;lt;br/&amp;gt;Adjust pH to 7.3. Filter Sterilized. Store at 4o&amp;lt;br/&amp;gt;C in full, tightly closed 50 ml tubes.&amp;lt;br/&amp;gt;1X Working Solution (lysing buffer)&amp;lt;br/&amp;gt;Add 5 ml 10X Stock Lysing Buffer to 45 ml H2O. Mix well. Store at room temperature for up to one week&lt;br /&gt;
&lt;br /&gt;
1X &amp;amp;nbsp;ACK (Ammonium Chloride Potassium)&lt;br /&gt;
&lt;br /&gt;
&amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; 155mM NH4Cl &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp;8.29g&lt;br /&gt;
&lt;br /&gt;
&amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; 10mM KHCO3 &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp;1.0g&lt;br /&gt;
&lt;br /&gt;
&amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; 0.1mM EDTA &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp; &amp;amp;nbsp;0.2 ml (500mM)&lt;br /&gt;
&lt;br /&gt;
RBC lysis buffer 10x&amp;lt;br/&amp;gt;1. Prepare 8,26 g of NH4Cl&amp;lt;br/&amp;gt;2. Add 1,19 g of NaHCO3&amp;lt;br/&amp;gt;3. Add 200 µL of EDTA [0,5 M, pH8]&amp;lt;br/&amp;gt;4. Add a.d until 100 mL&amp;lt;br/&amp;gt;5. Adjust pH to 7.3&amp;lt;br/&amp;gt;6. Filter sterile&amp;lt;br/&amp;gt;Note: to obtain 1x solution, dilute with a.d sterile&amp;amp;nbsp;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;br/&amp;gt;Erythrocyte Lysing Solution (no preservative) 10X Stock Solution&amp;lt;br/&amp;gt;Dissolve in 1 liter of H2O:&lt;br /&gt;
&lt;br /&gt;
89.9 g NH4Cl&amp;lt;br/&amp;gt;10.0 g KHCO3&amp;lt;br/&amp;gt;370.0 mg tetrasodium EDTA&amp;lt;br/&amp;gt;Adjust pH to 7.3. Store at 4°C in full, tightly closed 50 ml tubes.&amp;lt;br/&amp;gt;1X Working Solution&amp;lt;br/&amp;gt;Add 5 ml 10X Lysing Stock Solution to 45 ml H2O. Mix well. Store at room temperature for up to one week.&lt;br /&gt;
&lt;br /&gt;
Procedure&amp;lt;br/&amp;gt;Mix 14 ml Lysing Buffer to 1 ml Blood.&amp;lt;br/&amp;gt;Incubate for 3 - 5 minutes.&amp;lt;br/&amp;gt;Centrifuge at 300 x g for 5 minutes at room temperature.&amp;lt;br/&amp;gt;Aspirate supernatant and resuspend pellet in 5 ml of COLD Phosphate Buffered Saline (PBS).&amp;lt;br/&amp;gt;Centrifuge at 300 x g for 5 minutes at 2 - 8°C.&amp;lt;br/&amp;gt;Aspirate supernatant and resuspend pellet in 1 ml of COLD PBS with protein carrier.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
[[Category:Transfection]]&lt;/div&gt;</summary>
		<author><name>Paul.xu</name></author>
	</entry>
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