DNA实验技术 您的位置：首页 > 实验方法 DNA实验技术

Random Primer DNA Labeling

点击次数：  更新时间：2015/12/22 14:09:04  

　　For use with GibcoBRL Random Primer DNA labeling system.

　　Objective:

　　To produce radioactively labeled DNA strands for the detection of target DNA or RNA sequences in various applications including Southern and northern blot hybridization.

　　Required Materials

　　GibcoBRL Random Primer Labeling Kit

　　Random primers buffer mixture

　　dATP solution

　　dCTP solution

　　dGTP solution

　　dTTP solution

　　Klenow Fragment (Large Fragment of DNA Polymerase I)

　　Stop Buffer

　　Control DNA

　　dsDNA Fragment

　　Distilled Water

　　[a-32 P]dCTP

　　Radioactivity monitoring and waste management equipment

　　1 mL syringe

　　Sephadex G-50 saturated in TE buffer pH 7.4 , 0.2% SDS.

　　Procedures

　　Start=> You must first have a purified dsDNA fragment of known concentration that you wish to label.

　　1.Combine the following:

　　25 ng dsDNA fragment in 5-20μl dH2 O

　　2 μl dATP solution

　　2 μl dGTP solution

　　2 μl dTTP solution

　　15 μl Random Primer Buffer Mixture

　　5 μl [a-32 P]dCTP (approximately 50 uCi)

　　Distilled water to a volume of 49 μl

　　2.Mix briefly, and pulse down in a microcentrifuge.

　　3.Denature dsDNA by boiling for 5 minutes. Then immediately place on ice.

　　4.Add 1 μl Klenow Fragment, mix gently but thoroughly. If necessary, briefly pulse down contents in a microcentrifuge.

　　5.Incubate at room temperature (25 degrees Celsius) for 1 hour.

　　6.Add 2 μl of stop buffer.

　　To purify and/or determine the activity of incorporated dCTP- continue.

　　7.Dilute 2 μl of the 52 μl sample into 500 μl with 498 μl of distilled water for use later when determining total radioactivity.

　　8.Place a small amount of glass wool at the bottom of a 1 mL syringe.

　　9.Load sephadex G-50 (saturated in TE pH 7.4, 0.2% SDS) into the 1 mL syringe.

　　10.Pack the mini-column by spinning the 1 mL syringe in a 15 mL conical tube in a clinical centrifuge on a setting of 6 for 30 seconds.

　　11.Repeat steps 9 and 10 until the column fills the syringe to approximately 0.9 mL.

　　12.Add the remaining 50 μl of the labeling reaction onto the column. Rinse the labeling reaction with 50 μl TE pH 7.4 and add the rinse to the column.

　　13.Place a clean 1.5 mL microcentrifuge tube at the bottom of the 15 mL conical tube to collect your sample.

　　14.Spin the column in the clinical centrifuge for one minute on setting 6.

　　15.Add an additional 100 μl of TE pH 7.4 to the column and spin down for one minute at setting 6.

　　16.Check the volume of the collected sample and adjust to 200 μl if short.

　　17.Dilute 2 μl of the 200 μl sample into 125 μl by adding 123 μl of distilled water.

　　18.Label two Whatman GF/C filters, total and inc. Then spot the total filter with 5 μl of diluted probe from step 7 and spot the inc. filter with 5 μl of the diluted and purified probe from step 17.

　　19.Allow the filters to dry or dry under a heat lamp.

　　20.Check radioactivity in a liquid scintillation counter.

　　Total radioactivity(cpm) is equal to 2600 x cpm[total]

　　Incorporated radioactivity(cpm) is equal to 2500 x cpm[inc]

　　% incorporated is equal to (inc/50)/(total/52)*100

　　21.Store the probe at -20 degrees.