pDS472a
pDS472a
规格:
货期:
编号:TS138799
品牌:Testobio
| 产品名称： | pDS472a |
|---|---|
| 商品货号： | TS138799 |
| Designations： | pDS472a |
| Depositors： | SL Forsburg |
| Biosafety Level： | 1 |
| Vector Information： | Size (kb): 9.1999998092651370 Vector: pDS472a (phagemid) Promoters: Promoter for expression nmt1 (full strength) Construction: REP4X Marker(s):ampR,ura4+ Construct size (kb): 9.199999809265137 Features: marker(s): ampR marker(s): ura4+ promoter for expression: nmt1 (full strength) replicon: ars1 replicon: f1 replicon: pMB1 MCS: XhoI...SmaI tag (C-terminal): bacterial GST |
| Applications： | encodes removable tag for protein isolation expression vector |
| Comments： | Restriction digests of the clone give the following sizes (kb): HindIII--6.2, 1.9, 1.1; EcoRI--8.0, 1.2; PstI--9.2. The pDS472 5 oligo changed the ATG of GST to TTG (M1L) in order to prevent translation of only the GST portion of a fusion protein. The vector was designed for C-terminal tagging with GST (glutathione S transferase). The vector contains a thrombin cleavage site (LVPR/GS) immediately following the GST moiety, to allow removal of the tag following purification. The vector was constructed by 1) amplification of the Schistosoma japonicum glutathione S-transferase gene with primers designed to flank the gene and modify the polylinker, 2) gel purification and digest of the PCR product with XhoI, 3) ligation into pREP4X cleaved with XhoI and SmaI; the SmaI site was lost during cloning, 4) digestion with NotI & SalI, purified GST-containing fragment was cloned into pSLF172, digested with NotI and SalI. |
| Media： | ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin |
| Growth Conditions： | Temperature: 37.0°C |
| References： | Forsburg SL, Sherman DA. General purpose tagging vectors for fission yeast. Gene 191: 191-195, 1997. PubMed: 9218719 |
| Related Products： | component of:ATCC 87685 |
| Shipped： | freeze-dried |
首页 >
产品中心
>
微生物培养
>
菌株
>
null
>
pDS472a
产品中心 Product Center
联系我们CONTACT US
-
0574-87917803
24小时服务热线 -
testobio@163.com
销售邮箱 -
浙江省宁波市高新区晶辉路866弄33号智造港E4幢3楼
地址
联系方式
-
章丽敏
17757489010 -
朱静
18067106081 -
李晴
18067408036 -
李晶晶
13375187189 -
周雪
13372109301
| 产品名称： | pDS472a |
|---|---|
| 商品货号： | TS138799 |
| Designations： | pDS472a |
| Depositors： | SL Forsburg |
| Biosafety Level： | 1 |
| Vector Information： | Size (kb): 9.1999998092651370 Vector: pDS472a (phagemid) Promoters: Promoter for expression nmt1 (full strength) Construction: REP4X Marker(s):ampR,ura4+ Construct size (kb): 9.199999809265137 Features: marker(s): ampR marker(s): ura4+ promoter for expression: nmt1 (full strength) replicon: ars1 replicon: f1 replicon: pMB1 MCS: XhoI...SmaI tag (C-terminal): bacterial GST |
| Applications： | encodes removable tag for protein isolation expression vector |
| Comments： | Restriction digests of the clone give the following sizes (kb): HindIII--6.2, 1.9, 1.1; EcoRI--8.0, 1.2; PstI--9.2. The pDS472 5 oligo changed the ATG of GST to TTG (M1L) in order to prevent translation of only the GST portion of a fusion protein. The vector was designed for C-terminal tagging with GST (glutathione S transferase). The vector contains a thrombin cleavage site (LVPR/GS) immediately following the GST moiety, to allow removal of the tag following purification. The vector was constructed by 1) amplification of the Schistosoma japonicum glutathione S-transferase gene with primers designed to flank the gene and modify the polylinker, 2) gel purification and digest of the PCR product with XhoI, 3) ligation into pREP4X cleaved with XhoI and SmaI; the SmaI site was lost during cloning, 4) digestion with NotI & SalI, purified GST-containing fragment was cloned into pSLF172, digested with NotI and SalI. |
| Media： | ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin |
| Growth Conditions： | Temperature: 37.0°C |
| References： | Forsburg SL, Sherman DA. General purpose tagging vectors for fission yeast. Gene 191: 191-195, 1997. PubMed: 9218719 |
| Related Products： | component of:ATCC 87685 |
| Shipped： | freeze-dried |
