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peqGOLD 50 bp DNA-Ladder Orange G - Peqlab

peqGOLD 50 bp DNA-Ladder Orange G - Peqlab

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Data Sheet<br />

<strong>peqGOLD</strong> <strong>50</strong> <strong>bp</strong> <strong>DNA</strong>-<strong>Ladder</strong> <strong>Orange</strong> G<br />

'improved version'<br />

Lot-No. ........<br />

Concentration<br />

Usage<br />

0.1 mg <strong>DNA</strong>/ml<br />

1 µl (0.1 µg)/mm Lane<br />

Order-No. 25-23<strong>50</strong> 1 x <strong>50</strong> µg 1 x 1 ml <strong>Orange</strong> G Loading buffer for samples (6x)<br />

25-2351 5 x <strong>50</strong> µg 2 x 1 ml <strong>Orange</strong> G Loading buffer for samples (6x)<br />

Description<br />

<strong>peqGOLD</strong> <strong>50</strong> <strong>bp</strong> <strong>DNA</strong>-<strong>Ladder</strong> <strong>Orange</strong> G consists of fragments derived from specially digested <strong>DNA</strong><br />

of plasmid pEJ3, which contains pUC, λ phage and Yeast sequences. The marker is shipped 'ready-<br />

to-use'<br />

in Loading buffer (10 mM Tris-HCl (pH 7.6), 10 mM EDTA, 0.025 % <strong>Orange</strong> G, 0.005 %<br />

xylene cyanol and 10 % glycerol)<br />

13 Fragments 1000, 900, 800, 700, 600, <strong>50</strong>0, 400, 300, 2<strong>50</strong>, 200, 1<strong>50</strong>, 100 and <strong>50</strong> base pairs<br />

6x <strong>Orange</strong> G<br />

Loading buffer<br />

Note<br />

10 mM Tris-HCL (pH 7.6), 0.15 % <strong>Orange</strong> G, 0.03 % xylene cyanol, 60 % glycerol and 60 mM EDTA<br />

<strong>peqGOLD</strong> <strong>50</strong> <strong>bp</strong> <strong>DNA</strong>-<strong>Ladder</strong> <strong>Orange</strong> G is ideal for sizing of unknown <strong>DNA</strong> fragments in the range<br />

of <strong>50</strong> to 1031 base pairs. Additional weak bands might occur in agarose gels which result from<br />

circular forms of <strong>DNA</strong> ligation products.<br />

The 'improved version' is characterized by equalized amounts of <strong>DNA</strong> per band for easier<br />

quantification. The 1031 <strong>bp</strong> fragment was replaced by a 1000 <strong>bp</strong> fragment. The <strong>50</strong>0 <strong>bp</strong> and the 2<strong>50</strong><br />

<strong>bp</strong> fragments were introduced as new reference bands.<br />

Loading<br />

Agarose and non-denaturing Polyacrylamide gels:<br />

<strong>peqGOLD</strong> <strong>50</strong> <strong>bp</strong> <strong>DNA</strong>-<strong>Ladder</strong> <strong>Orange</strong> G is ready-to-use and can be applied directly to the gel:<br />

Vortex marker briefly.<br />

Load 1 µl (0.1 µg) <strong>DNA</strong>-<strong>Ladder</strong> per 1 mm lane width<br />

Visualize fragments after electrophoretic separation by ethidium bromide-staining. Do not heat before<br />

loading. <strong>50</strong> µg marker are sufficient for approx. 100 lanes (5 mm Lane width).<br />

<strong>Peqlab</strong>_V0911_E<br />

info@peqlab.com · www.peqlab.com


<strong>peqGOLD</strong> <strong>50</strong> <strong>bp</strong> <strong>DNA</strong>-<strong>Ladder</strong> <strong>Orange</strong> G<br />

Quantification<br />

See the graph for the percentage of the bands and the<br />

amount of <strong>DNA</strong> per band in ng, relating to 0.5 µg loaded<br />

marker. Use the same volume of <strong>DNA</strong> and marker.<br />

Additionally the concentration of loading buffer in samples<br />

and marker should be equal.<br />

Note<br />

Ethidium bromide migrates contrarily to the <strong>DNA</strong> during<br />

electrophoresis. Therefore the distribution of ethidium<br />

bromide in the gel is not constant. To ensure equal<br />

distribution of ethidium bromide in the gel add 0.5 mg/l<br />

ethidium bromide to electrophoresis buffer or dye the gel after<br />

the run.<br />

Shipment: blue ice<br />

Storage: + 4 °C/– 20 °C<br />

Stability: up to 6 months at + 4 °C<br />

minimum 18 months at – 20 °C<br />

<strong>Peqlab</strong>_V0911_E<br />

info@peqlab.com · www.peqlab.com

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