Assembly pcr - Revision history

Christopher C Vanlang at 21:10, 23 December 2011

2011-12-23T21:10:56Z

←Older revision		Revision as of 21:10, 23 December 2011
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	This technique worked great for assembling Biobricks, especially GFP with promoters, etc. I started using this back when I was running into trouble with 3-way assembly and thought this might save a step if it worked. It worked really well in that context using [http://www.invitrogen.com/content/sfs/manuals/11306016.pdf PCR supermix].		This technique worked great for assembling Biobricks, especially GFP with promoters, etc. I started using this back when I was running into trouble with 3-way assembly and thought this might save a step if it worked. It worked really well in that context using [http://www.invitrogen.com/content/sfs/manuals/11306016.pdf PCR supermix].
	**However, recently tried this again with a plasmid that contained repeats using Phusion PCR and even the self-mix Platinum PCR (Invitrogen), and couldn't get it to work... :( Be wary of repeats.		**However, recently tried this again with a plasmid that contained repeats using Phusion PCR and even the self-mix Platinum PCR (Invitrogen), and couldn't get it to work... :( Be wary of repeats.
		+
		+	==See Also==
		+	*[[PCR]]
		+	*[[PCR Techniques]]

	[[Category:Protocol]] [[Category:In vitro]] [[Category:DNA]]		[[Category:Protocol]] [[Category:In vitro]] [[Category:DNA]]

Felix Moser: /* Notes */

2009-06-30T18:09:53Z

Notes

←Older revision		Revision as of 18:09, 30 June 2009
Line 26:		Line 26:
	==Notes==		==Notes==
	[[User:Felix Moser\|Felix Moser]] 14:08, 30 June 2009 (EDT)		[[User:Felix Moser\|Felix Moser]] 14:08, 30 June 2009 (EDT)
-	This technique worked great for ~~putting together biobricke~~, especially GFP with promoters, etc. I was running into trouble with 3-way assembly and thought this might save a step if it worked. ~~Worked~~ really well in that context using [http://www.invitrogen.com/content/sfs/manuals/11306016.pdf PCR supermix].	+	This technique worked great for assembling Biobricks, especially GFP with promoters, etc. I started using this back when I was running into trouble with 3-way assembly and thought this might save a step if it worked. It worked really well in that context using [http://www.invitrogen.com/content/sfs/manuals/11306016.pdf PCR supermix].
-	**However, recently tried this again with a plasmid that contained repeats using Phusion PCR and even the self-mix Platinum PCR (~~Initrogen~~), and couldn't get it to work... :(	+	**However, recently tried this again with a plasmid that contained repeats using Phusion PCR and even the self-mix Platinum PCR (Invitrogen), and couldn't get it to work... :( Be wary of repeats.

	[[Category:Protocol]] [[Category:In vitro]] [[Category:DNA]]		[[Category:Protocol]] [[Category:In vitro]] [[Category:DNA]]

Felix Moser at 18:08, 30 June 2009

2009-06-30T18:08:11Z

←Older revision		Revision as of 18:08, 30 June 2009
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	by [[User:Felix Moser\|Felix Moser]]		by [[User:Felix Moser\|Felix Moser]]
		+
		+	==Notes==
		+	[[User:Felix Moser\|Felix Moser]] 14:08, 30 June 2009 (EDT)
		+	This technique worked great for putting together biobricke, especially GFP with promoters, etc. I was running into trouble with 3-way assembly and thought this might save a step if it worked. Worked really well in that context using [http://www.invitrogen.com/content/sfs/manuals/11306016.pdf PCR supermix].
		+	**However, recently tried this again with a plasmid that contained repeats using Phusion PCR and even the self-mix Platinum PCR (Initrogen), and couldn't get it to work... :(

	[[Category:Protocol]] [[Category:In vitro]] [[Category:DNA]]		[[Category:Protocol]] [[Category:In vitro]] [[Category:DNA]]

Felix Moser at 19:29, 30 March 2009

2009-03-30T19:29:39Z

←Older revision		Revision as of 19:29, 30 March 2009
Line 1:		Line 1:
	{{back to protocols}}		{{back to protocols}}
	==Introduction==		==Introduction==
-	Assembly PCR can be used to assemble two pieces of DNA into one piece ~~without endonuclease and ligation steps~~. Briefly, it essentially involves PCR'ing the two pieces separately with primers that have a 20bp overlap and then doing an extra PCR step using the two products as the template. This is essentially just for ease of cloning. Instead of trying to PCR two separate pieces and then assemble them by endonuclease digestion and ligation, it can be easier simply to PCR the first piece w/ a reverse primer that overlaps with the forward primer of the second piece, and then use the product of the first PCR reactions as a template for the assembly reaction. If ~~the overlap of~~ the reverse primer for the 5' piece and the forward primer for the 3' piece overlap by ~20bp, the product of the first PCR reactions should anneal in the overlapping region and create a full length product. Using the Fw primer for the first piece and the ~~Rev~~ primer for the second piece in the assembly reaction then amplifies the desired full-length product. The ~~great~~ merits for this technique are that it's arguably faster than standard 3-way ligation assembly (because you need good-quality DNA to make that work well, which usually means sub-cloning each piece), and it's more reliable (the quality of the product is very good so you can clone it directly into the desired vector; in my hands, PCR assembly has worked ~~everytime i~~'ve tried it (~8times)).	+	Assembly PCR can be used to assemble two gene-sized pieces of DNA into one piece for easier cloning of fusion genes/parts. Briefly, it essentially involves PCR'ing the two pieces separately with primers that have a 20bp overlap and then doing an extra PCR step using the two products as the template. This is essentially just for ease of cloning. Instead of trying to PCR or cut out of a vector two separate pieces and then assemble them by endonuclease digestion and ligation (aka 3-way ligation), it can be easier simply to PCR the first piece w/ a reverse primer that overlaps with the forward primer of the second piece, and then use the product of the first PCR reactions as a template for the assembly reaction. If the reverse primer for the 5' piece and the forward primer for the 3' piece overlap by ~20bp, the product of the first PCR reactions should anneal in the overlapping region and create a full length (gene fusion) product. Using the forward primer for the first piece and the reverse primer for the second piece in the assembly reaction then amplifies the desired full-length product. The merits for this technique are that it's arguably faster than standard 3-way ligation assembly (because you need good-quality DNA to make that work well, which usually means sub-cloning each piece, in my experience), and it's more reliable (the quality of the product is very good so you can clone it directly into the desired vector; in my hands, PCR assembly has worked every time I've tried it (~8times)).

	==Method==		==Method==
-	Remember that this technique ~~works only~~ if: You want to ~~assembly~~ in series two pieces of DNA from PCR product (or you already have one piece you want to cut out and assemble in series w/ a PCR product; in this case it's easier just to do the PCR for the piece you already have. Believe me, the assembly reaction product is well worth the cost of the extra primers and PCR step).	+	Remember, that this technique is good if: You want to assemble in series two long pieces of DNA from PCR product.

-	*1) Design the reverse primer for the DNA that will be 5' w/ significant overlap w/ the forward primer for the 3' piece. Essentially, as long as one of the primers has ~20bp overlap w/ the reverse complement of the other primer, the products should anneal in the assembly reaction.	+	*1) Design the reverse primer for the DNA that will be 5' w/ significant overlap w/ the forward primer for the 3' piece. Essentially, as long as one of the primers has ~20bp overlap w/ the 'reverse complement' of the other primer, the products should anneal in the assembly reaction.

	*2) Do PCR as normal for the two (5' and the 3') pieces using the longer primers that correspond to each piece.		*2) Do PCR as normal for the two (5' and the 3') pieces using the longer primers that correspond to each piece.

-	*3) Check on a gel to make sure you got product from the first PCR reaction. Some people like to cut out the product band and use the purified products as template for the next reaction. I just use the PCR product straight from the first reactions w/o any purification; the logic is that the undesired primers/templates will be in such low concentrations that the intended reaction will be highly favored. Besides, if the residual "middle" primers did create product, they would just be making more starting template!	+	*3) Check on a gel to make sure you got product from the first PCR reaction. Some people like to cut out the product band and use the purified products as template for the next reaction. I just use the PCR product straight from the first reactions w/o any purification; the logic is that the undesired primers/templates will be in such low concentrations that the intended reaction will be highly favored. Besides, if the residual "middle" primers did create product, they would just be making more starting template, which shouldn't hurt your rxn.

-	*4) Set up the assembly reaction like a regular PCR, except: 1) as template use equal amounts of product from the first reactions, and 2)use the Forward primer for the 5' piece and the Reverse primer for the 3' piece to amplify the annealed template. (I use 45µl of Invitrogen Taq HIFI supermix, 2µl of 5µM primer each, and 0.5µl of each PCR product as template). Cycle like you did for the first reactions.	+	*4) Set up the assembly reaction like a regular PCR, except: 1) as template use equal amounts of product from the first reactions, and 2)use the Forward primer for the 5' piece and the Reverse primer for the 3' piece to amplify the annealed template. (I use 45µl of Invitrogen Taq HIFI supermix, 2µl of 5µM primer each, and 0.5µl of each PCR product as template). Cycle like you did for the first reactions, except w/ longer extension time corresponding to the length of your product.

	*5) Run the product on a gel. If the reaction worked, you should see a band the size of the sum of your two templates.		*5) Run the product on a gel. If the reaction worked, you should see a band the size of the sum of your two templates.

-	*6) Purify the product (I use the Quiagen PCR pur. kit), cut w/ desired endonucleases, and clone away! The quality of the product from this reaction is usually very good and I can get up to >100 transformants.	+	*6) Purify the product (I use the Quiagen PCR pur. kit), cut w/ desired endonucleases, and clone away! The quality of the product from this reaction is usually very good and very plentyful and I can get up to >100 transformants.
		+
		+	*7) An arguable disadvantage of this technique, besides slightly higher up-front cost for primers, is that it requires sequencing following assembly to make sure the PCR rxn hasn't produced mutations. Use HiFi polymerase and you shouldn't really have a problem, though... but don't be lazy: you should still get your clones sequenced.
		+
		+	*Also: If you already have one piece that you've cloned successfully and you want to cut out and assemble in series w/ the second piece (a PCR product), I still think it's it's easier just to do the PCR for the piece you already have cloned. For me, the assembly reaction product is well worth the cost of the extra primers (<$20) and PCR step.

	by [[User:Felix Moser\|Felix Moser]]		by [[User:Felix Moser\|Felix Moser]]

	[[Category:Protocol]] [[Category:In vitro]] [[Category:DNA]]		[[Category:Protocol]] [[Category:In vitro]] [[Category:DNA]]

Torsten Waldminghaus at 17:32, 23 February 2009

2009-02-23T17:32:26Z

←Older revision		Revision as of 17:32, 23 February 2009
Line 1:		Line 1:
		+	{{back to protocols}}
	==Introduction==		==Introduction==
	Assembly PCR can be used to assemble two pieces of DNA into one piece without endonuclease and ligation steps. Briefly, it essentially involves PCR'ing the two pieces separately with primers that have a 20bp overlap and then doing an extra PCR step using the two products as the template. This is essentially just for ease of cloning. Instead of trying to PCR two separate pieces and then assemble them by endonuclease digestion and ligation, it can be easier simply to PCR the first piece w/ a reverse primer that overlaps with the forward primer of the second piece, and then use the product of the first PCR reactions as a template for the assembly reaction. If the overlap of the reverse primer for the 5' piece and the forward primer for the 3' piece overlap by ~20bp, the product of the first PCR reactions should anneal in the overlapping region and create a full length product. Using the Fw primer for the first piece and the Rev primer for the second piece in the assembly reaction then amplifies the desired full-length product. The great merits for this technique are that it's arguably faster than standard 3-way ligation assembly (because you need good-quality DNA to make that work well, which usually means sub-cloning each piece), and it's more reliable (the quality of the product is very good so you can clone it directly into the desired vector; in my hands, PCR assembly has worked everytime i've tried it (~8times)).		Assembly PCR can be used to assemble two pieces of DNA into one piece without endonuclease and ligation steps. Briefly, it essentially involves PCR'ing the two pieces separately with primers that have a 20bp overlap and then doing an extra PCR step using the two products as the template. This is essentially just for ease of cloning. Instead of trying to PCR two separate pieces and then assemble them by endonuclease digestion and ligation, it can be easier simply to PCR the first piece w/ a reverse primer that overlaps with the forward primer of the second piece, and then use the product of the first PCR reactions as a template for the assembly reaction. If the overlap of the reverse primer for the 5' piece and the forward primer for the 3' piece overlap by ~20bp, the product of the first PCR reactions should anneal in the overlapping region and create a full length product. Using the Fw primer for the first piece and the Rev primer for the second piece in the assembly reaction then amplifies the desired full-length product. The great merits for this technique are that it's arguably faster than standard 3-way ligation assembly (because you need good-quality DNA to make that work well, which usually means sub-cloning each piece), and it's more reliable (the quality of the product is very good so you can clone it directly into the desired vector; in my hands, PCR assembly has worked everytime i've tried it (~8times)).

Felix Moser: /* Method */

2008-07-06T22:52:32Z

Method

←Older revision		Revision as of 22:52, 6 July 2008
Line 9:		Line 9:
	*2) Do PCR as normal for the two (5' and the 3') pieces using the longer primers that correspond to each piece.		*2) Do PCR as normal for the two (5' and the 3') pieces using the longer primers that correspond to each piece.

-	*3) Check on a gel to make sure you got product from the first PCR reaction. Some people like to cut out the product band and use the purified products as template for the next reaction. I just use the PCR product straight from the first reactions w/o any purification; the logic is that the undesired primers/templates will be in such low concentrations that the intended reaction will be highly favored. Besides, if the ~~residueal~~ "middle" primers did create product, they would just be making more starting template!	+	*3) Check on a gel to make sure you got product from the first PCR reaction. Some people like to cut out the product band and use the purified products as template for the next reaction. I just use the PCR product straight from the first reactions w/o any purification; the logic is that the undesired primers/templates will be in such low concentrations that the intended reaction will be highly favored. Besides, if the residual "middle" primers did create product, they would just be making more starting template!

	*4) Set up the assembly reaction like a regular PCR, except: 1) as template use equal amounts of product from the first reactions, and 2)use the Forward primer for the 5' piece and the Reverse primer for the 3' piece to amplify the annealed template. (I use 45µl of Invitrogen Taq HIFI supermix, 2µl of 5µM primer each, and 0.5µl of each PCR product as template). Cycle like you did for the first reactions.		*4) Set up the assembly reaction like a regular PCR, except: 1) as template use equal amounts of product from the first reactions, and 2)use the Forward primer for the 5' piece and the Reverse primer for the 3' piece to amplify the annealed template. (I use 45µl of Invitrogen Taq HIFI supermix, 2µl of 5µM primer each, and 0.5µl of each PCR product as template). Cycle like you did for the first reactions.

Felix Moser: /* Method */

2008-07-06T22:51:30Z

Method

←Older revision		Revision as of 22:51, 6 July 2008
Line 9:		Line 9:
	*2) Do PCR as normal for the two (5' and the 3') pieces using the longer primers that correspond to each piece.		*2) Do PCR as normal for the two (5' and the 3') pieces using the longer primers that correspond to each piece.

-	*3) Check on a gel to make sure you got product from the first PCR reaction. Some people like to cut out the product band and use the purified products as template for the next reaction. I just use the PCR product straight from the first reactions w/o any purification; the logic is that the undesired primers/templates will be in such low concentrations that the intended reaction will be highly favored.	+	*3) Check on a gel to make sure you got product from the first PCR reaction. Some people like to cut out the product band and use the purified products as template for the next reaction. I just use the PCR product straight from the first reactions w/o any purification; the logic is that the undesired primers/templates will be in such low concentrations that the intended reaction will be highly favored. Besides, if the residueal "middle" primers did create product, they would just be making more starting template!

	*4) Set up the assembly reaction like a regular PCR, except: 1) as template use equal amounts of product from the first reactions, and 2)use the Forward primer for the 5' piece and the Reverse primer for the 3' piece to amplify the annealed template. (I use 45µl of Invitrogen Taq HIFI supermix, 2µl of 5µM primer each, and 0.5µl of each PCR product as template). Cycle like you did for the first reactions.		*4) Set up the assembly reaction like a regular PCR, except: 1) as template use equal amounts of product from the first reactions, and 2)use the Forward primer for the 5' piece and the Reverse primer for the 3' piece to amplify the annealed template. (I use 45µl of Invitrogen Taq HIFI supermix, 2µl of 5µM primer each, and 0.5µl of each PCR product as template). Cycle like you did for the first reactions.

Felix Moser: /* Method */

2008-07-06T22:50:11Z

Method

←Older revision		Revision as of 22:50, 6 July 2008
Line 7:		Line 7:
	*1) Design the reverse primer for the DNA that will be 5' w/ significant overlap w/ the forward primer for the 3' piece. Essentially, as long as one of the primers has ~20bp overlap w/ the reverse complement of the other primer, the products should anneal in the assembly reaction.		*1) Design the reverse primer for the DNA that will be 5' w/ significant overlap w/ the forward primer for the 3' piece. Essentially, as long as one of the primers has ~20bp overlap w/ the reverse complement of the other primer, the products should anneal in the assembly reaction.

-	*2) Do PCR as normal for the 5' and the 3' pieces using the longer primers that correspond to each piece.	+	*2) Do PCR as normal for the two (5' and the 3') pieces using the longer primers that correspond to each piece.

	*3) Check on a gel to make sure you got product from the first PCR reaction. Some people like to cut out the product band and use the purified products as template for the next reaction. I just use the PCR product straight from the first reactions w/o any purification; the logic is that the undesired primers/templates will be in such low concentrations that the intended reaction will be highly favored.		*3) Check on a gel to make sure you got product from the first PCR reaction. Some people like to cut out the product band and use the purified products as template for the next reaction. I just use the PCR product straight from the first reactions w/o any purification; the logic is that the undesired primers/templates will be in such low concentrations that the intended reaction will be highly favored.

Felix Moser: /* Introduction */

2008-07-06T22:48:25Z

Introduction

←Older revision		Revision as of 22:48, 6 July 2008
Line 1:		Line 1:
	==Introduction==		==Introduction==
-	Assembly PCR can be used to assemble two pieces of DNA into one piece without endonuclease and ligation steps. Briefly, it essentially involves PCR'ing the two pieces separately with primers that have a 20bp overlap and then doing an extra PCR step using the two products as the template. This is essentially just for ease of cloning. Instead of trying to PCR two separate pieces and then assemble them by endonuclease digestion and ligation, it can be easier simply to PCR the first piece w/ a reverse primer that overlaps with the forward primer of the ~~soon-to-be adjacent~~ piece, and then use the product of the first PCR reactions as a template for the assembly reaction. If the overlap of the reverse primer for the 5' piece and the forward primer for the 3' piece overlap by ~20bp, the product of the first PCR reactions should anneal in the overlapping region and create a full length product. Using the Fw primer for the first piece and the Rev primer for the second piece in the assembly reaction then amplifies the desired full-length product. The great merits for this technique are that it's arguably faster than standard 3-way ligation assembly (because you need good-quality DNA to make that work well, which usually means sub-cloning each piece), and it's more reliable (the quality of the product is very good so you can clone it directly into the desired vector; in my hands, PCR assembly has worked everytime i've tried it (~8times)).	+	Assembly PCR can be used to assemble two pieces of DNA into one piece without endonuclease and ligation steps. Briefly, it essentially involves PCR'ing the two pieces separately with primers that have a 20bp overlap and then doing an extra PCR step using the two products as the template. This is essentially just for ease of cloning. Instead of trying to PCR two separate pieces and then assemble them by endonuclease digestion and ligation, it can be easier simply to PCR the first piece w/ a reverse primer that overlaps with the forward primer of the second piece, and then use the product of the first PCR reactions as a template for the assembly reaction. If the overlap of the reverse primer for the 5' piece and the forward primer for the 3' piece overlap by ~20bp, the product of the first PCR reactions should anneal in the overlapping region and create a full length product. Using the Fw primer for the first piece and the Rev primer for the second piece in the assembly reaction then amplifies the desired full-length product. The great merits for this technique are that it's arguably faster than standard 3-way ligation assembly (because you need good-quality DNA to make that work well, which usually means sub-cloning each piece), and it's more reliable (the quality of the product is very good so you can clone it directly into the desired vector; in my hands, PCR assembly has worked everytime i've tried it (~8times)).

	==Method==		==Method==

Felix Moser: /* Introduction */

2008-07-06T22:44:18Z

Introduction

←Older revision		Revision as of 22:44, 6 July 2008
Line 1:		Line 1:
	==Introduction==		==Introduction==
-	Assembly PCR can be used to assemble two pieces of DNA into one piece. Briefly, it essentially involves PCR'ing the two pieces separately with primers that have a 20bp overlap and then doing an extra PCR step using the two products as the template. This is essentially just for ease of cloning. Instead of trying to PCR two separate pieces and then assemble them by endonuclease digestion and ligation, it can be easier simply to PCR the first piece w/ a reverse primer that overlaps with the forward primer of the soon-to-be adjacent piece, and then use the product of the first PCR reactions as a template for the assembly reaction. If the overlap of the reverse primer for the 5' piece and the forward primer for the 3' piece overlap by ~20bp, the product of the first PCR reactions should anneal in the overlapping region and create a full length product. Using the Fw primer for the first piece and the Rev primer for the second piece in the assembly reaction then amplifies the desired full-length product. The great merits for this technique are that it's arguably faster than standard 3-way ligation assembly (because you need good-quality DNA to make that work well, which usually means sub-cloning each piece), and it's more reliable (the quality of the product is very good so you can clone it directly into the desired vector; in my hands, PCR assembly has worked everytime i've tried it (~8times)).	+	Assembly PCR can be used to assemble two pieces of DNA into one piece without endonuclease and ligation steps. Briefly, it essentially involves PCR'ing the two pieces separately with primers that have a 20bp overlap and then doing an extra PCR step using the two products as the template. This is essentially just for ease of cloning. Instead of trying to PCR two separate pieces and then assemble them by endonuclease digestion and ligation, it can be easier simply to PCR the first piece w/ a reverse primer that overlaps with the forward primer of the soon-to-be adjacent piece, and then use the product of the first PCR reactions as a template for the assembly reaction. If the overlap of the reverse primer for the 5' piece and the forward primer for the 3' piece overlap by ~20bp, the product of the first PCR reactions should anneal in the overlapping region and create a full length product. Using the Fw primer for the first piece and the Rev primer for the second piece in the assembly reaction then amplifies the desired full-length product. The great merits for this technique are that it's arguably faster than standard 3-way ligation assembly (because you need good-quality DNA to make that work well, which usually means sub-cloning each piece), and it's more reliable (the quality of the product is very good so you can clone it directly into the desired vector; in my hands, PCR assembly has worked everytime i've tried it (~8times)).

	==Method==		==Method==