ISISBio:Protocols/p11 resin preparation - Revision history

Cameron Neylon at 15:07, 1 August 2008

2008-08-01T15:07:50Z

←Older revision		Revision as of 15:07, 1 August 2008
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	[[Category:Chromatography]]		[[Category:Chromatography]]
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Cameron Neylon at 11:11, 29 April 2008

2008-04-29T11:11:16Z

←Older revision		Revision as of 11:11, 29 April 2008
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	==Overview==		==Overview==

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	# Suspend the resin in at least 20 volumes of water and allow to settle for at least 30 minutes		# Suspend the resin in at least 20 volumes of water and allow to settle for at least 30 minutes
	## Pour off supernatant, resuspend and repeat at least 8-10 times.		## Pour off supernatant, resuspend and repeat at least 8-10 times.
-	##~~Step 3 has multiple sub-steps within~~ it.	+	##* This may appear appointless but it is crucial for getting rid of fine particles that will increase back pressure and reduce column performance.
-	##~~Enumerate each~~ of ~~those~~.	+	# Suspend the resin in 0.2 M NaOH,allow to settle for at least 30 minutes.
		+	## Pour of supernatant and repeat until pH of supernatant is higher than 10
		+	# Suspend resin in water, allow to settle, pour off supernatant, and repeat until pH is seven or lower
		+	# Suspend resin in 0.2 M HCl, allow to settle, pour off supernatant, and repeat until pH is three or lower
		+	# Suspend resin in storage buffer, allow to settle, pour of supernatant, and repeat until pH is that of buffer
		+	#* Try to leave the resin at least once overnight in buffer at some point in this step
		+	# Suspend resin and pour carefully into column housing
		+	# If resin is to be stored, consider adding 0.2% sodium azide
		+	# Try to replace the buffer regularly as ammonia can be released from amine containing buffers

	==Notes==		==Notes==
-	#~~List troubleshooting tips here.~~	+	# The repeated washing with water is critical to remove fines. Don't be tempted to shortcut this step!
-	~~#You can also link~~ to ~~FAQs/tips provided by other sources such as the manufacturer or other websites~~.	+
-	~~#Anecdotal observations that might~~ be ~~of use~~ to ~~others can also be posted here.~~	+

	Please sign your name to your note by adding <font face="courier"><nowiki>'''*~~~~''':</nowiki></font> to the beginning of your tip.		Please sign your name to your note by adding <font face="courier"><nowiki>'''*~~~~''':</nowiki></font> to the beginning of your tip.

	==References==		==References==
-	~~'''Relevant papers and books'''~~
	<!-- If this protocol has papers or books associated with it, list those references here. See the [[OpenWetWare:Biblio]] page for more information. -->		<!-- If this protocol has papers or books associated with it, list those references here. See the [[OpenWetWare:Biblio]] page for more information. -->
-	~~<biblio>~~
-	~~#Goldbeter-PNAS-1981 pmid=6947258~~
-	~~#Jacob-JMB-1961 pmid=13718526~~
-	~~#Ptashne-Genetic-Switch isbn=0879697164~~
-	~~</biblio>~~
-
	==Contact==		==Contact==
-	*~~Who has experience with this protocol?~~	+	* [[User:Cameron_Neylon\|Cameron Neylon]]

-	~~or instead, [[Talk:{{PAGENAME}}\|discuss this protocol]].~~

	<!-- You can tag this protocol with various categories. See the [[Categories]] page for more information. -->		<!-- You can tag this protocol with various categories. See the [[Categories]] page for more information. -->
	[[Category:Protocol]]		[[Category:Protocol]]
-	~~[[Category:Needs attention]] <!--Delete this line once the protocol is complete-->~~

-	~~<!-- Move the relevant categories above this line to tag your protocol with the label~~
	[[Category:In vitro]]		[[Category:In vitro]]
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		+	[[Category:Protein]]
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		+	[[Category:Chromatography]]
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	[[Category:In vivo]]		[[Category:In vivo]]
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-	~~[[Category:Protein]]~~	+

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Cameron Neylon: New page: ==Overview== Preparation of Whatmann P11 Phosphocellulose resin for cation exchange chromatography. Phosphocellulose remains a useful and cheap cation exchange resin and is particularly...

2008-04-29T10:53:49Z

New page: ==Overview== Preparation of Whatmann P11 Phosphocellulose resin for cation exchange chromatography. Phosphocellulose remains a useful and cheap cation exchange resin and is particularly...

New page

==Overview==

Preparation of Whatmann P11 Phosphocellulose resin for cation exchange chromatography.

Phosphocellulose remains a useful and cheap cation exchange resin and is particularly good for the final stages of purification of DNA binding proteins. The preparation of the resin for optimum performance is somewhat tedious but carefull attention to detail will yield a higher performance coplumn with lower back pressure.

==Materials==

* Whatmann P11 Phosphocelluose resin
* Purified water
* 0.2 M NaOH
* 0.2 M HCl
* Storage buffer (Tris-HCl pH 7.6 is a common choice)

==Procedure==
# Weigh out approximately as many grams of resin as millilitres of column will be required into a large container with at least 20-fold larger volume
# Suspend the resin in at least 20 volumes of water and allow to settle for at least 30 minutes
## Pour off supernatant, resuspend and repeat at least 8-10 times.
##Step 3 has multiple sub-steps within it.
##Enumerate each of those.

==Notes==
#List troubleshooting tips here.
#You can also link to FAQs/tips provided by other sources such as the manufacturer or other websites.
#Anecdotal observations that might be of use to others can also be posted here.

Please sign your name to your note by adding <font face="courier"><nowiki>'''*~~~~''':</nowiki></font> to the beginning of your tip.

==References==
'''Relevant papers and books'''

<biblio>
#Goldbeter-PNAS-1981 pmid=6947258
#Jacob-JMB-1961 pmid=13718526
#Ptashne-Genetic-Switch isbn=0879697164
</biblio>

==Contact==
*Who has experience with this protocol?

or instead, [[Talk:{{PAGENAME}}|discuss this protocol]].


[[Category:Protocol]]
[[Category:Needs attention]]