d*b
2 楼
N900那linux,N8那Sybian 3, 现在N9的meego,都是test drive, N8的所谓Anna,叫
嚣了快半年了吧?我看年底能给你们update算不错了
linux再寡,apple当年再落魄,人还有铁杆粉丝追随,nokia这玩意做的,连铁杆粉丝
都被丫的强奸了,早点卖给比尔盖茨回瑞典织鱼网去那才是正路
嚣了快半年了吧?我看年底能给你们update算不错了
linux再寡,apple当年再落魄,人还有铁杆粉丝追随,nokia这玩意做的,连铁杆粉丝
都被丫的强奸了,早点卖给比尔盖茨回瑞典织鱼网去那才是正路
c*o
3 楼
Hi folks,
I try to purify a peptide(AMP) from the bacteria broth culture. It looks
like that so much sugar from the broth tightly bound with the protein even
after HPLC and centricon pufication. I still find the dark sugar color in
the active fraction. and this is a big problem for the later SDS-PAGE
running since suger blocks the gel pore, I can not get a band......always
smear. Does somebody have experience to romove suger?
thanks for your time and help.
I try to purify a peptide(AMP) from the bacteria broth culture. It looks
like that so much sugar from the broth tightly bound with the protein even
after HPLC and centricon pufication. I still find the dark sugar color in
the active fraction. and this is a big problem for the later SDS-PAGE
running since suger blocks the gel pore, I can not get a band......always
smear. Does somebody have experience to romove suger?
thanks for your time and help.
N*S
5 楼
根据最新消息,装 anna的机器下个月开始卖,老机器升级在8月份,一般提前半个月就
可以自己下载到。
可以自己下载到。
s*e
6 楼
dialysis?
n*7
7 楼
送中国店?
K*S
9 楼
Are you sure those are sugar?
【在 c*****o 的大作中提到】![](/moin_static193/solenoid/img/up.png)
: Hi folks,
: I try to purify a peptide(AMP) from the bacteria broth culture. It looks
: like that so much sugar from the broth tightly bound with the protein even
: after HPLC and centricon pufication. I still find the dark sugar color in
: the active fraction. and this is a big problem for the later SDS-PAGE
: running since suger blocks the gel pore, I can not get a band......always
: smear. Does somebody have experience to romove suger?
: thanks for your time and help.
【在 c*****o 的大作中提到】
![](/moin_static193/solenoid/img/up.png)
: Hi folks,
: I try to purify a peptide(AMP) from the bacteria broth culture. It looks
: like that so much sugar from the broth tightly bound with the protein even
: after HPLC and centricon pufication. I still find the dark sugar color in
: the active fraction. and this is a big problem for the later SDS-PAGE
: running since suger blocks the gel pore, I can not get a band......always
: smear. Does somebody have experience to romove suger?
: thanks for your time and help.
x*n
10 楼
太浪费了,旱的旱死,涝的涝死
c*o
12 楼
it should be the sugar. The culture broth contains high ammount of glucose(
20g/L), so after autoclave the broth color is dark brown. active fraction
eluted from HPLC has even more dark color.
it also looks like difficult to diaysis....
20g/L), so after autoclave the broth color is dark brown. active fraction
eluted from HPLC has even more dark color.
it also looks like difficult to diaysis....
s*3
13 楼
真是好浪费啊,要是离的近,我就去买了。
b*l
14 楼
,叫
粉丝
粉丝
s*9
15 楼
"so much sugar from the broth tightly bound with the protein even
after HPLC and centricon pufication"
Sounds wired... How did you do your HPLC?
after HPLC and centricon pufication"
Sounds wired... How did you do your HPLC?
m*u
17 楼
Nokia马上要跟随微软了,现在做的这些产品...算是对过去的研发努力有所交代吧.
M*a
18 楼
no idea what happened. could it be possible to use Ca2+ for competing
binding and replace glucose?
【在 c*****o 的大作中提到】![](/moin_static193/solenoid/img/up.png)
: Hi folks,
: I try to purify a peptide(AMP) from the bacteria broth culture. It looks
: like that so much sugar from the broth tightly bound with the protein even
: after HPLC and centricon pufication. I still find the dark sugar color in
: the active fraction. and this is a big problem for the later SDS-PAGE
: running since suger blocks the gel pore, I can not get a band......always
: smear. Does somebody have experience to romove suger?
: thanks for your time and help.
binding and replace glucose?
【在 c*****o 的大作中提到】
![](/moin_static193/solenoid/img/up.png)
: Hi folks,
: I try to purify a peptide(AMP) from the bacteria broth culture. It looks
: like that so much sugar from the broth tightly bound with the protein even
: after HPLC and centricon pufication. I still find the dark sugar color in
: the active fraction. and this is a big problem for the later SDS-PAGE
: running since suger blocks the gel pore, I can not get a band......always
: smear. Does somebody have experience to romove suger?
: thanks for your time and help.
n*w
20 楼
why you add glucose to your culture medium? to lower the background?
y*3
21 楼
我的也是头发丝,xmjd啊
y*3
22 楼
开花了做韭花酱啊
n*7
23 楼
冻上冬天吃
y*8
33 楼
包成饺子冻起来最好。直接冻的话叶子会烂的吧?
l*o
38 楼
浪费啊。。。
我家的全割了也只有一点点。
我家的全割了也只有一点点。
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