GeneSpin Srl
Via Friuli, 51
20135 Milano
P.IVA C.F. 04520270960
Laboratory
and sales office
c/o Fondazione Filarete
Viale Ortles, 22/4
20139 Milano
tel. +39 02 56660199
fax. +39 02 537250
Endpoint PCR Green Line
2X XtraWhite Master Mix and 2X XtraRTL Master Mix (GeneSpin proprietary formulation), are two premixed, ready-to-use solution containing Xtra-Taq Pol, dNTPs and MgCl2 in a Reaction Buffer optimized for use in PCR amplification of targets present in low copy number and to avoid amplification of non-specific products. Both buffers contain 3.0mM magnesium, PCR enhancers and thickening agents (vortex thoroughly prior to use). 2X Master Mix Standard GL contain an internal fluorescent stain for DNA detection on Agarose gel directly after PCR amplification.
2X XtraRTL Master Mix contains Orange G dye that allows gel loading and electrophoresis of the sample directly from the PCR tube, without further manipulation. 2X XtraWhite Master Mix is supplied with appropriate quantity of 6X Loading Dye. The Orange G dye migrates at the same rate as a duplex DNA fragment of approximately 50 Kbp and does not interfere with DNA migration when it is used as a loading dye for agarose gel electrophoresis.
STS-XMMixW 200* GL
5ml
2X XtraWhite Master Mix GL
STS-XMMixW 1000* GL
25ml
2X XtraWhite Master Mix GL
STS-XMMixRTL 200 GL
5ml
2X XtraRTL Master Mix GL
STS-XMMixRTL 1000 GL
25ml
2X XtraRTL Master Mix GL
*2X XtraWhite Master Mix GL is supplied with appropriate quantity of 6X Loading Dye
FOR RESEARCH USE ONLY
UNIT DEFINITION
One unit is defined as the amount of enzyme required to incorporate 10 nanomoles of dNTPs into acid-insolubile material in 30 min at 74°C.
SHIPPING
Shipped in green ice.
STORAGE
Store at -20C°
SHELF LIFE
12 months
FORM
Liquid
CONCENTRATION
2X conc.
GREEN LINE OVERVIEW
2X Master Mix GL contain an internal fluorescent stain for DNA detection on Agarose gel directly after PCR amplification.
component
primers
DNA Template
MG Water
2X Master Mix GL
Assay Set-Up:
Before starting, vortex all components thoroughly to ensure homogeneity.
Prepare a premix for the number of assays you need according to the following protocol:
stock conc.
final conc.
2X
1X
15.0ul
1ug/ul each
50ng/ul each
-
-
10-20ng
-
-
30ul reaction
2.0ul each
up to 30ul
1)The annealing temperature depends on the melting temperature of the primers used.
2)The elongation time depends on the length of the fragments to be amplified. A time
of 1 min/kb is recommended.
Cycling conditions:
Spin down the tubes/plate briefly to remove bubbles and place them into the cycler.
denaturation
denaturation (1)
annealing (2)
extension
95°C
95°C
50-68°C
72°C
5min
30 sec
30 sec
30 sec
4 min
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administration@pec.genespin.com
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