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| 产品名称： | pEC145RM102-18/39 |
|---|---|
| 商品货号： | TS183527 |
| Designations： | pEC145RM102-18/39 |
| Species： | Xanthomonas campestris (Pammel) Dowson pathovar badrii |
| Depositors： | New England Biolabs, Inc., I Schildkraut, New England Biolabs, Inc. |
| Applications： | in suitable host, produces protein modification methylase XbaI in suitable host, produces protein restriction endonuclease XbaI |
| Vector： | Construct size (kb): 5.699999809265137 |
| Insert： | DNA: genomic Insert lengths(kb): 3.0 Gene product: restriction endonuclease XbaI hsdM Target Gene: modification methylase XbaI, restriction endonuclease XbaI |
| Insert Size (kb)： | 3.0 |
| 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. |
| Comments： | Restriction digests of the clone give the following sizes (kb): XbaI--5.7; EcoRI--5.7; HindIII--2.7, 1.3, 1.1, 0.4, 0.3. The insert contains 3 internal HindIII sites, generating fragments from the insert of 1.3, 1.1, 0.25, and 0.35 kb. |
| References： | Van Cott EM, Wilson GG. Method for producing the XbaI restriction endonuclease and methylase. US Patent 4,983,542 dated Jan 8 1991 Van Cott EM, Wilson GG. Cloning the FnuDI, NaeI, NcoI and XbaI restriction-modification systems. Gene 74: 55-59, 1988. PubMed: 3074019 |
| 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. |