丁香实验_LOGO
登录
提问
我要登录
|免费注册
点赞
收藏
wx-share
分享

DNA extraction from hair...help-Molecular Biology

互联网

943

Hi....I need a protocol for extracting DNA from hair/roots...(specifically horse)...and any additional information such as  storage pr℃edure/timing/etc....thanks....

-tree-

--------------------------------------------------------------------------------

if anyone is curious, i found a protocol from Quiagen....thanks

-tree-

--------------------------------------------------------------------------------

Hi,

Having a look at your problem I remember that I have seen some protocol for DNA extraction from hair in the Bio-Rad site.

Try it and good luck!

-diliana-

--------------------------------------------------------------------------------

I use either of these two methods

1.DNA Extraction from hair:

Cut 10- 15 hair roots about 0.5 cm into a 1.5ml eppendorf tube.

Add 50 μl of 200mM NaOH solution.

Boil the tube in a water bath at 94℃ for 10 minutes.

Cool at room temperature and add 50 μl of a solution containing 200mM HCL.

+100mM Tris-HCL pH 8.5.

Your DNA is ready for PCR.

10mM Tris pH 8.3

50mM KCL

0.5% Tween

Also add 10μl of 20ug/ml solution of Proteinase K in 10mM Tris-HCL (pH 7.5)

Vortex for 30 seconds.

Ultracentrifuge at 13000 rpmfor 1 second.

Incubate overnight in a 56 - 60℃ waterbath.

Incubate for 10 minutes at 94℃ ( to denature the proteinase K  I presume)

Cool down to room temperature.

Ultracentrifuge at 13000 rpm for 1 second.

Ready DNA for your PCR.

Do not hesitate to get in touch incase of any further queries.

-Djibrial-

--------------------------------------------------------------------------------

I use either of these two methods

1.DNA Extraction from hair:

Cut 10- 15 hair roots about 0.5 cm into a 1.5ml eppendorf tube.

Add 50 μl of 200mM NaOH solution.

Boil the tube in a water bath at 94℃ for 10 minutes.

Cool at room temperature and add 50 μl of a solution containing 200mM HCL.

+100mM Tris-HCL pH 8.5.

Your DNA is ready for PCR.

10mM Tris pH 8.3

50mM KCL

0.5% Tween

Also add 10μl of 20ug/ml solution of Proteinase K in 10mM Tris-HCL (pH 7.5)

Vortex for 30 seconds.

Ultracentrifuge at 13000 rpmfor 1 second.

Incubate overnight in a 56 - 60℃ waterbath.

Incubate for 10 minutes at 94℃ ( to denature the proteinase K  I presume)

Cool down to room temperature.

Ultracentrifuge at 13000 rpm for 1 second.

Ready DNA for your PCR.

Do not hesitate to get in touch incase of any further queries.

-Djibrial-

--------------------------------------------------------------------------------

Hi,

I had received more info:  for horse hair, use 2mm of 3 hairs (from the root end) because it is pretty coarse...

I did this, following the Quiagen protocol, and was able to isolate DNA.....

 thanks for all the hints....

-tree-

--------------------------------------------------------------------------------

Hi

Does anyone know how can I purify the hairs before the extraction?

I am sure that the hairs covered with all kinds of bacteria which their DNA will be contain in the final solution.

what is the amount of the DNA extracted from hair?

thanks

-shaytzur-

--------------------------------------------------------------------------------

提问
扫一扫
丁香实验小程序二维码
实验小助手
丁香实验公众号二维码
扫码领资料
反馈
TOP
打开小程序