If you don't care about the price, you may want to try Sigma's kit. I don't remember the name,but it is very quick and efficient.
【在 c*********u 的大作中提到】 : No, I mean the PCR kit for genotyping. this kit can be used for the dirty : and unpurified DNA sample.
q*i
13 楼
赶紧扫描了发过去,打印出来
w*l
14 楼
自己配吧,十分简单又便宜!
s*9
15 楼
自己准备不充分赖FEDEX干嘛啊。
s*e
16 楼
we use a digestion kit from Zygem for embryonic tissue, it does save a lot of time
r*o
17 楼
正解
【在 q*********i 的大作中提到】 : 赶紧扫描了发过去,打印出来
h*n
18 楼
I guess you mean extract-n-amp. Sometimes it does not make good DNA for PCR, its PCR master mix is good. So I go back to DNeasy.
t
【在 O******e 的大作中提到】 : If you don't care about the price, you may want to try Sigma's kit. I don't : remember the name,but it is very quick and efficient.
自己配的, 网上搜了搜,这是跟我们完全一样的protocol Final concentration of tail digestion buffer (TDB): 50 mM KCl 10 mM Tris-HCl (pH 9.0) 0.1 % Triton X-100 0.4 mg/ml Proteinase K Add 100 ul of TDB per tail piece (2-5 mm) in a microcentrifuge tube. Be careful not to cut too much tail. Incubate the tube at either 60 C for 3 hours, with gentle mixing every 30 minutes, or 55 C overnight. Incubate the tube at 94 C (or boil) for 10 minutes to denature the Proteinase K. Spin in microcentrifuge at top speed for 15 minutes.
We use Sigma's RedTaq for mouse genotyping (tail). It does not need to add DNA sample buffer (loading dye) to your PCR products, so you can directly load your PCR samples to agarose gel and run.