DT301
DT301
规格:
货期:
编号:TS178038
品牌:Testobio
| 产品名称： | DT301 |
|---|---|
| 商品货号： | TS178038 |
| Designations： | DT301 |
| Species： | Corynebacterium diphtheriae (Kruse) Lehmann and Neumann |
| Depositors： | President and Fellows of Harvard College, JR Murphy, President and Fellows of Harvard College |
| Vector： | Construct size (kb): 0.0 Insert ends: Sau3A1 DESCRIPTION OF VECTOR COMPONENT: Name of vector: pUC8 Intact vector size: 2.700 Type of vector: plasmid Cloning sites: EcoRI SmaI XmaI BamHI SalI AccI HincII PstI HindIII Polylinker sites: EcoRI SmaI XmaI BamHI SalI AccI HincII PstI HindIII Construction: pBR322, Escherichia coli lacZalpha, M13mp8 Host range: Escherichia coli Features (with orientation and position when available): enhancer: none insert detection: lacZ marker(s): ampR promoter: lac replicon: pMB1 terminator: none Cross references: |
| Insert： | DNA: genomic DESCRIPTION OF INSERT COMPONENT: Genome: Corynebacterium diphtheriae Gene name: diphtheria toxin, fragment B Contains complete coding sequence?: U Type of DNA: genomic Insert end: Insert end: Insert size (kb): Cross references: Gene product: diphtheria toxin, fragment B |
| Media： | ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin |
| Biosafety Level： | 1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country. |
| Shipping Information： | Distributed: freeze-dried |
| Comments： | Restriction digests of the clone give the following sizes (kb): EcoRI--4.2. Constructed by cloning a Sau3A1 fragment from the tox gene including all of the fragment B gene. Fragment cloned is depicted as fragment B in Fig. 3 of US Patent 4,675,382 dated June 23, 1987. Constructed from pUC8 and a small segment of the Corynebacteriophage beta tox-197 genome. |
| References： | Murphy JR. Hybrid protein. US Patent 4,675,382 dated Jun 23 1987 |
| Disclosure： | This material is cited in a US or other Patent and may not be used to infringe the claims. Depending on the wishes of the Depositor, ATCC may be required to inform the Patent Depositor of the party to which the material was furnished. This material may not have been produced or characterized by ATCC. |
首页 >
产品中心
>
微生物培养
>
菌株
>
null
>
DT301
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： | DT301 |
|---|---|
| 商品货号： | TS178038 |
| Designations： | DT301 |
| Species： | Corynebacterium diphtheriae (Kruse) Lehmann and Neumann |
| Depositors： | President and Fellows of Harvard College, JR Murphy, President and Fellows of Harvard College |
| Vector： | Construct size (kb): 0.0 Insert ends: Sau3A1 DESCRIPTION OF VECTOR COMPONENT: Name of vector: pUC8 Intact vector size: 2.700 Type of vector: plasmid Cloning sites: EcoRI SmaI XmaI BamHI SalI AccI HincII PstI HindIII Polylinker sites: EcoRI SmaI XmaI BamHI SalI AccI HincII PstI HindIII Construction: pBR322, Escherichia coli lacZalpha, M13mp8 Host range: Escherichia coli Features (with orientation and position when available): enhancer: none insert detection: lacZ marker(s): ampR promoter: lac replicon: pMB1 terminator: none Cross references: |
| Insert： | DNA: genomic DESCRIPTION OF INSERT COMPONENT: Genome: Corynebacterium diphtheriae Gene name: diphtheria toxin, fragment B Contains complete coding sequence?: U Type of DNA: genomic Insert end: Insert end: Insert size (kb): Cross references: Gene product: diphtheria toxin, fragment B |
| Media： | ATCC® Medium 1227: LB Medium (ATCC medium 1065) with 50 mcg/ml ampicillin |
| Biosafety Level： | 1
Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country. |
| Shipping Information： | Distributed: freeze-dried |
| Comments： | Restriction digests of the clone give the following sizes (kb): EcoRI--4.2. Constructed by cloning a Sau3A1 fragment from the tox gene including all of the fragment B gene. Fragment cloned is depicted as fragment B in Fig. 3 of US Patent 4,675,382 dated June 23, 1987. Constructed from pUC8 and a small segment of the Corynebacteriophage beta tox-197 genome. |
| References： | Murphy JR. Hybrid protein. US Patent 4,675,382 dated Jun 23 1987 |
| Disclosure： | This material is cited in a US or other Patent and may not be used to infringe the claims. Depending on the wishes of the Depositor, ATCC may be required to inform the Patent Depositor of the party to which the material was furnished. This material may not have been produced or characterized by ATCC. |
