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384-well PCR实验方法

互联网2013-09-06

2629

Beforehand.

http://molbiol.ru/eng ;
e-mail: editor@molbiol.ru

Solutions.

PCR buffer 10x

(store at +4^o C):

	Conc.	Stock	500ml
Tris Cl, pH 8.undefined	0.5M	1M	250ml
KCl	0.5M	2M	125ml
MgCl₂	15mM	1M	7.5ml
Tween 20	1%	100% p=1.108	5.0ml 5.54g
H₂ O		mQ	112.5ml

	Conc.	Stock	500ml
Tris Cl, pH 8.undefined	0.5M	1M	250ml
KCl	0.5M	2M	125ml
MgCl₂	15mM	1M	7.5ml
Tween 20	1%	10%	50ml
H₂ O		mQ	67.5ml

p (10x Buf.) = 1.018 g/ml
~undefined - another possibility: 175ml (1M Trise-base) + 75ml(1M Trise-HCl).

PCR buffer 2.5x

(store at +4^o C)

	Conc.	Stock	100ml	300ml
Buffer (15mM MgCl₂ )	2.5x	10x	25ml	75ml
Betaine	3.75M	5M	74.75ml	224.25ml
Cresol red (Na)	125 µM	50mM	250 µl	0.75ml

p (2.5x buffer) = 1.06g/ml

PCR mix

Store working quantity at +4^o C; the main stock at -20^o C. It is possible to keep PCR mixture with enzymes at at +4^o C for about 15h without any decrease of efficiency of PCR reaction.

	Conc.	Stock	72.5mundefined~K~Hfont~M_~K~Ha~M~K~Hfont~M~K~Htd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~Ktd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~0~Kfont~M~Ka_name~L~4s3~4~M_~Kfont~M_~K~Hfont~M~K~Ha~M~K~Hfont~M~K~Htd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~K~Htr~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~Ktr~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~Ktd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~0~Kfont~M~Ka_name~L~4s3~4~M~Kfont~MPCR_buffer~K~Hfont~M_~K~Ha~M~K~Hfont~M~K~Htd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~Ktd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~0~Kfont~M~Ka_name~L~4s3~4~M~Kfont~M1x~K~Hfont~M_~K~Ha~M~K~Hfont~M~K~Htd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~Ktd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~0~Kfont~M~Ka_name~L~4s3~4~M~Kfont~M2.5x~K~Hfont~M_~K~Ha~M~K~Hfont~M~K~Htd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~Ktd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~0~Kfont~M~Ka_name~L~4s3~4~M~Kfont~M29ml~K~Hfont~M_~K~Ha~M~K~Hfont~M~K~Htd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~Ktd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~0~Kfont~M~Ka_name~L~4s3~4~M_~Kfont~M_~K~Hfont~M~K~Ha~M~K~Hfont~M~K~Htd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~K~Htr~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~Ktr~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~Ktd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~0~Kfont~M~Ka_name~L~4s3~4~M~Kfont~MdNTP’s	0.2mM	25mM	580µl
Primer#1 & #2	200pmol/ml	?	? µl
H₂ O		mQ	?ml
Taq/Pfu poundefined*~K~Hfont~M_~K~Ha~M~K~Hfont~M~K~Htd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~Ktd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~0~Kfont~M~Ka_name~L~4s3~4~M~Kfont~M50~F250u~Hml~K~Hfont~M_~K~Ha~M~K~Hfont~M~K~Htd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~Ktd~M~2~1~0~0~0~0~0~0~0~0~0~0~0~0~0~0~Kfont~M~Ka_name~L~4s3~4~M~Kfont~M~Nu~H_µl	?µl

~undefined*_~F_Taq~Au~B~IPfu~Au~B~L100~I1.~K~Hfont~M_~K~Ha~M~K~Hfont~M~K~Hp~M~Ka_name~L~4s3~4~M~2~1~0~0~0~0~0~0~Kfont~M~K~Hfont~M~K~Ha~M~Kfont~M~Ka_name~L~4s3~4~M_~Kfont~M_~K~Hfont~M~K~Ha~M~K~Hfont~M~Ka_name~L~4s3~4~M~2~1~0~0~0~0~0~Kfont~M~K~Hfont~M~K~Ha~M~Kfont~M~Ka_name~L~4s3~4~M~Kfont~M_~K~Hfont~M~K~Ha~M~K~Hfont~M~K~Hdiv~M~Ka_name~L~4s3~4~M~2~1~0~0~0~0~Kfont~M~K~Hfont~M~K~Ha~M~Kfont~M~Ka_name~L~4s3~4~M~Kfont~M_~K~Hfont~M~K~Ha~M~K~Hfont~M~K~Htd~M~2~1~0~0~K~Htr~M~2~1~0~K~Htbody~M~2~1~K~Htable~M~K~Ha~M~2~1~Ktable~M~2~1~0~Ktbody~M~2~1~0~0~Ktr~M~2~1~0~0~0~Ktd~M~2~1~0~0~0~0~Kdiv~M~2~1~0~0~0~0~0~Kbr_~H~M~2~1~0~0~0~0~0~Kp_class~L~4h2~4~M~2~1~0~0~0~0~0~0~Kfont~M~Ka_name~L~4k~4~M_~Kfont~MComments.~K~Hfont~M_~K~Ha~M~K~Hfont~M~K~Hp~M~Ka_name~L~4k~4~M~2~1~0~0~0~0~0~K~Ha~M~Kp_class~L~4h3~4~M~Ka_name~L~4k~4~M~2~1~0~0~0~0~0~0~K~Ha~M~Ka_name~L~4k~4~M~K~Ha~M~Ka_name~L~4kp~4~M_~Kfont~MDetailed_instructions~E_step_by_step~K~Hfont~M_~K~Ha~M~K~Hp~M~Ka_name~L~4kp~4~M~2~1~0~0~0~0~0~K~Ha~M~Ka_name~L~4kp~4~M_~2~1~0~0~0~0~0~Kp_class~L~4pn~4~M~2~1~0~0~0~0~0~0~Kfont~M~51.~K~Hfont~M~K~Hp~M~2~1~0~0~0~0~0~K~Ha~M~Kul~M~Ka_name~L~4kp~4~M~2~1~0~0~0~0~0~0~Kli~M~2~1~0~0~0~0~0~0~0~Kp_class~L~4pn~4~M~2~1~0~0~0~0~0~0~0~0~Kfont~M~53.~K~Hfont~M~K~Hp~M~2~1~0~0~0~0~0~0~0~Kul~M~2~1~0~0~0~0~0~0~0~0As_a_first_approximation_for_the_annealing_temperature_of_primers_one_can_use_the_Tmelting_value_given_by_the_program_~4Oligo~4._Take_into_account_that_betaine_addition_would_probably_decrease_the_annealing_temperature_~Asucrose_has_no_effect_on_it~B._For_example~E_for_the_primer_pair_M~F13~H23_and_M~F13~H30_maximum_annealing_temperature_decreased_from_71o_C_to_67o_C_when_1.5M_betaine_was_added.~2~1~0~0~0~0~0~0~0~K~Hul~M~2~1~0~0~0~0~0~0~K~Hli~M~2~1~0~0~0~0~0~0~Kli~M~2~1~0~0~0~0~0~0~0~Kfont~MIt_is_convenient_to_have~I~Kbr_~H~M~2~1~0~0~0~0~0~0~undefined all four dNTP's mix (100mM or 25mM stocks);
~undefined primers mix.

#4.

Frozen bacteria plates have to be placed on a bench in one layer one by one, separately. This prevents condensation of liquid on the inner side of the cover and transfer of liquid between wells. Condensation occurs when temperature of the cover becomes lower than temperature of the liquid in the plate. It is convenient to use an air fan to accelerate thawing.

#6.

12.2ml per plate, if PCR volume is 30µl/well (maximum for old ABT-384 plates #TF-0384) or 16.3ml per plate, if PCR volume is 40µl/well (maximum for new ABT-384 plates #AB-0937).

Add the enzyme last. We were told that Pfu polymerase can destroy primers if PCR mix stored for too long at room temperature. Therefore, just before you add the enzyme, in front of you should be labeled PCR plates, the reservoir for multi-channel pipette, bacterial plates and the replicators. We have tested that it is possible to keep PCR mixture with enzymes at +4^o C for about 15h without any decrease of efficiency of PCR reaction.

After the PCR mix is aliquoted into plates, transfer the remaining volume to 50ml Falcon tube and keep it at -20^o C. You can use it for the subsequent experiments (with the same primers), thus minimizing the volume of new PCR master-mix which needs to be prepared.

#8.

Optional ― remove air bubbles from bottom of the wells.

#9.

You need twice as much replicators as number of PCR-plates. Insert replicator from the nearest edge, holding it leaned at 5-10^o so that the nearest pins are closer to the plate (the row "P" in the PCR plate). The pins should be directed to the center of the wells.

The purpose of double inoculation is not to increase amount of transferred material but rather to decrease the probability of no transfer at all.

It is better to mix bacteria in the plate by replicator before transfer. Try to avoid mixing in only one direction, because it can induce sticking of partually lysed bacteria to the needles of replicator.

The volume of media captured on one needle of the replicator is ca 0.2µl.

In theory, the plates with inoculated bacteria can be stored at -20^o C before PCR up to a few weeks. However, do not freeze them on dry ice. Instead, just put them in the freezer or on the towel soaked with the liquid nitrogen. If freezed on dry ice, evaporating CO₂ will shift the pH. If betain- or sucrose-containing PCR mix was used, most likely PCR would succeed anyway, but you don't want be unsure about it, do you?

The same precautions should be taken for the PCR/NaOH mixtures for spotting. It is possible to freeze them in dry ice (for about 0.5 - 1h) only if they are sealed by "Tesafilm" or "Adhesive Sealing Sheet".

#10.

Sealing films: the best is the office tape from TESA (Tesafilm #2826775): (i) easily taped and removable; (ii) reliable; (iii) cheap - about 10DM per roll. Much worse variants:

ABgene : (hardly removable, expensive);
Microseal "A" film. Fragile: don't press the PCR machine cover very tightly, it can damage Microseal "A", it shrinks after PCR and unsuitable for freezing. For Microseal "A" film:
- when PCR is finished - immediately (plate still in the PCR block) take off the upper film;
- take the plates out of PCR machine;
- remove the isolating film layer;
- get rid of the PCR mix which is in between wells with the yellow tip connected to the vacuum pump;
- use soft blotting paper to remove liquid from the plate surface;
- cover with the "Genetix" covers;
"Bio-stat" film. It has to be sealed tightly, e.g. using the backside of the marker to help. One can put a piece of thin rubber on top, as well. Funny: there were cases when PCR's worked fine with a quite sloppily attached Bio-stat film. In that case considerable volume was evaporated uniformly from each well. Probably there is some sort of equilibrium inside the PCR block so that the content of the well does not dry out completely.

For 384-PCR it is better to change the parameter exceed of temperature of the lid "Setup/Lid/Tracking/Lid offset" from the default 15^o C to 5^o C.

PCR-mix: our impression, that in general betaine is slightly worsening PCR reaction. The enzyme speed and activity became lower. But it is impossible to exclude betaine from the buffer for 384 plates. Without it we observed smear, differing from PCR plate to plate (in an 8-strip from the same PCR-mix PCR worked fine). Adding of sucrose has similar effect - the smear partially disappeared, but with betaine - completely.

If a sub-cycle PCR is used (see below) the product yield is more stable and a little bit higher (probably it is because of low-melting regions in some sequences). We used the following program:

Step:	T (^o C):	Time:
1	95	1:00
2	94	0:15
3	59	0:15
4	65	0:55
5	go to 3	2 add. times
6	go to 2	29 add. times
7	68	10:00
8	4	0
9	END

#11.

Lift each four edges carefully and hold the plate with your hand. Avoid the abrupt moves, if not, your PCR ends up on the cover.

The plate holder for 384-plates can be treated with "Teflon spray", then the plate can be removed easier.

#14.

Concentration should be more then 0.15µg/µl.

PCR方法相关产品:

move the plates to +4^o C and then to -20^o C;
centrifuge at ~800 rpm, 3' NT;
control PCR by agarose gel electrophoresis: 0.5 - 1µl from 5 - 15 wells;
seal the plates again;
move the plates to +4^o C and then to -20^o C;
for long term storage - -70^o C (keep track in your lab book!).
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