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全部话题 - 话题: digester
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w*******y
发帖数: 60932
1
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w*******y
发帖数: 60932
w*******y
发帖数: 60932
3
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X***h
发帖数: 74
4
来自主题: Biology版 - 有一个digestion的问题
如果我PCR后的product比较干净,能否不处理直接restriction digest? 现在我比较麻
烦的是如
果用column purification总是丢失大部分的DNA,后面digest完了还要gel
purification,
那就所剩无几了。
或者用SAP 去除primers,然后Ethanol-sodium acetate precipitation,总可以上
digestion了吧。
s******r
发帖数: 2876
5
来自主题: Biology版 - 有一个digestion的问题
你既然都P出来了,完全可以用PCR产物第二次扩增一遍,
DNA还不是要多少有多少。

如果我PCR后的product比较干净,能否不处理直接restriction digest? 现在我比较麻
烦的是如
果用column purification总是丢失大部分的DNA,后面digest完了还要gel
purification,
那就所剩无几了。
或者用SAP 去除primers,然后Ethanol-sodium acetate precipitation,总可以上
digestion了吧。
S******e
发帖数: 393
6
想用SalI-NheI double digetion,
NEB suggest sequential,
但我看到SalI和EcoRI double digestion 用 E.coRI buffer
NheI 和 EcoRI double digestion 也用E.coRI buffer
是不是SalI-NheI double digestion 就可以用E.coRI buffer,
而不用sequential了?
多谢回答!
e******0
发帖数: 2149
7
现在在用LC/MS/MS做一个膜蛋白的定量,试过run western blots的同时做in gel
digestion 然后LCMSMS,也试过in solution digestion.听别人说过似乎in gel
digestion比in solution的效率高,但我感觉in gel technically 难做些。至今两个
方法做出来的结果差别不大。想听下前辈们的意见,哪个方法会好些。多谢!
w*******y
发帖数: 60932
8
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w*******y
发帖数: 60932
9
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w*******y
发帖数: 60932
10
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w*******y
发帖数: 60932
11
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发帖数: 60932
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w*******y
发帖数: 60932
13
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w*******y
发帖数: 60932
14
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w*******y
发帖数: 60932
15
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w*******y
发帖数: 60932
16
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w*******y
发帖数: 60932
17
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w*******y
发帖数: 60932
c***e
发帖数: 111
19
来自主题: shopping版 - Reader's Digest 催我要钱
不知道该发哪里,就来这里求助大家了。n个月前,在Reader's Digest上Enter了一个
抽奖,结果没注意他下面有个小小的checkbox订阅他们的杂志,我没有主动uncheck,
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它自说自话来划钱了。而且我根本没想订杂志(虽然事实是我没有uncheck那个b... 阅读全帖
D*a
发帖数: 6830
20
来自主题: Biology版 - genotyping digestion buffer
Quick Tail Prep
Collect 1 mg skin biopsy (= normal size tail or figure tip) in 0.5 ml
Eppendorf tube.
Add 100 microliter of quick tail digestion buffer (below).
Incubate @ 56 C several hours to overnight.
Vortex and incubate @ 99 C, 10 minutes.
Centrifuge @ max speed, 5 minutes.
(NB i don't vortex so i don't need to centifuge the tube, it works)
Use 1-2 microliter aliquot of supernatant for a 25-50 microliter PCR
reaction (or whatever you routinely do).
Transfer supernatant to a fresh tube for s... 阅读全帖
D*a
发帖数: 6830
21
来自主题: Biology版 - genotyping digestion buffer
Quick Tail Prep
Collect 1 mg skin biopsy (= normal size tail or figure tip) in 0.5 ml
Eppendorf tube.
Add 100 microliter of quick tail digestion buffer (below).
Incubate @ 56 C several hours to overnight.
Vortex and incubate @ 99 C, 10 minutes.
Centrifuge @ max speed, 5 minutes.
(NB i don't vortex so i don't need to centifuge the tube, it works)
Use 1-2 microliter aliquot of supernatant for a 25-50 microliter PCR
reaction (or whatever you routinely do).
Transfer supernatant to a fresh tube for s... 阅读全帖
y****6
发帖数: 196
22
来自主题: Biology版 - antibody digestion
Thanks for sinister and kaka1000's reply. I labeled the antibody with
fluorescent dyes and quenchers, and I want to digest the antibody to small
fragments to break the FRET between dyes and quenchers. It would be best if
I can digest the antibody into the smallest fragments. Papain may not be the
best choice as it only cut antibody into three pieces. Maybe I can use some
kind of protease mixture? Any suggestion is welcome.
s******s
发帖数: 1584
23
两种Digestion没区别 要是担心Digestion 不完全多加点Trypsin就好了
膜蛋白我推荐In Gel
f******h
发帖数: 609
24
5个包子答谢:求一篇 2009 IEEE intermag conference 的 digest
找不到会议的CD了, 哪位仁兄还有的话能否帮我email一份? Please note it's not the paper. I have the 6page paper. I want the 2page digest from the conference CD.
FD-02 Spin polarized transport and dynamics in magnetic tunneling structures.
万分感激! 我的地址: h******[email protected]
f******h
发帖数: 609
25
5个包子答谢:求一篇 2009 IEEE intermag conference 的 digest
找不到会议的CD了, 哪位仁兄还有的话能否帮我email一份? Please note it's not the paper. I have the 6page paper. I want the 2page digest from the conference CD.
FD-02 Spin polarized transport and dynamics in magnetic tunneling structures.
万分感激! 我的地址: h******[email protected]
w*******y
发帖数: 60932
26
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w*******y
发帖数: 60932
w*******y
发帖数: 60932
28
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w*******y
发帖数: 60932
29
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w*******y
发帖数: 60932
30
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w*******y
发帖数: 60932
31
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w*******y
发帖数: 60932
w*******y
发帖数: 60932
33
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w*******y
发帖数: 60932
34
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w*******y
发帖数: 60932
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w*******y
发帖数: 60932
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w*******y
发帖数: 60932
37
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w*******y
发帖数: 60932
38
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w*******y
发帖数: 60932
39
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w*******y
发帖数: 60932
40
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x****5
发帖数: 1564
41
来自主题: Golf版 - 最新一期golf digest
1. get your stance in "sink"
2.put your takeaway on slow-mo
3. stop your backswing before you start down
4.make a "one-piece" downswing
5. anchor your right foot
sorry it is in the current golf magazine, not golf digest
d****9
发帖数: 3206
42
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x******r
发帖数: 367
43
Hello!
Is there anywhere that I can buy Readers Digest and Times in China?
Thank you very much.
a********a
发帖数: 3176
44
Reader's Digest has been out of business.
x******r
发帖数: 367
45
I am just asking if it is possible to get Readers Digest issues after 2000,
not necessarily the most current one.
Thanks.
l***r
发帖数: 459
46
I met a strange problem on JDBCRealm:
In my server.xml, it looks like:
className="org.apache.catalina.realm.JDBCRealm"
debug="99"
driverName="com.mysql.jdbc.Driver"
connectionURL="jdbc:mysql://localhost/auth"
connectionName="user"
connectionPassword="password"
userTable="users"
userNameCol="user_name"
userCredCol="user_pass"
userRoleTable="user_roles"
roleNameCol="role_name"
digest="MD5"
/>
It works if I use FORM authentication. So I am sure
mysql driver and MD5 are working fine. But it d
M******t
发帖数: 555
47
digest 100ug plasmid DNA 最小体积多少啊?
谢谢.
m******5
发帖数: 1383
48
google N-chip和X-chip
两种不同的方法
用酶digest的非特异性binding少,并且因为去掉了cross linking的步骤,能用的抗体
数大大增加。缺点是很难拿到transcriptional factor和特定片断的binding 。做
Histon的人应该用得多些,但因为没有cross linking,也会引入很多非特异性的
nucleosome remodeling。
用sonication 以及cross linking配合的方法好处是拿到的相互作用理论上说更接近生
理条件,但因为引入了固定这个过程,也导致许多artificial 作用, 比如蛋白质,
DNA间非功能性的相互作用
s******u
发帖数: 81
49
多谢!
另外的原因可能还有digestion enzyme的sequence preference.
说到co-IP, lysis buffer一般都加detergent吗?看别人的文章基本都加,可有的
interaction加了detergent几乎检测不到。

stringency
m******t
发帖数: 109
50
来自主题: Biology版 - genotyping digestion buffer
i want to know the digestion buffer for genotyping that doesnot purify
genomic DNA.i forgot it. let me know. thx.
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