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| 产品名称： | pJB124RM4-11 purified plasmid DNA |
|---|---|
| 商品货号： | TS197215 |
| Designations： | pJB124RM4-11 purified plasmid DNA |
| Depositors： | New England Biolabs, Inc., I Schildkraut, New England Biolabs, Inc. |
| Applications： | produces protein modification methylase HinPI produces protein restriction endonuclease HinPI |
| Vector： | Vector: pBR322 Vector type: plasmid Vector size (kb): 4.36 Markers: tetR, ampR (not functional in this clone) Vector ends: PstI |
| Insert： | Insert size (kb): 6.1 Gene: Modification methylase HinPI, restriction endonuclease HinP1 DNA : Genomic Source : Haemophilus influenzae biogroup aegyptius strain P1 (ATCC 53700) Insert ends: PstI |
| 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： | 150 ng dried plasmid DNA |
| Comments： | Restriction digests of the clone give the following sizes (kb): BamHI--10.6; EcoRI--6.4, 4.3; PstI--4.3 (doublet), 1.55. Insert contains the following restriction sites (approximate kb from the 5 end): BglII--1.0; ClaI--0.9; HindIII--5.4; PstI--1.5; PvuII--0.5, 5.5. |
| References： | Barsomian JM, Wilson GG. Method for producing the HinPI restriction endonuclease and methylase. US Patent 4,983,522 dated Jan 8 1991 Barsomian JM, et al. Cloning of the HhaI and HinPI restriction-modification systems. Gene 74: 5-7, 1988. PubMed: 3074018 |
| 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. |