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购买须知
| 产品名称： | pEagRM2.9 pEag RM2.9 |
|---|---|
| 商品货号： | TS163415 |
| Designations： | pEagRM2.9 pEag RM2.9 |
| Species： | Pantoea agglomerans (Beijerinck) Gavini et al. |
| Depositors： | New England Biolabs, Inc., I Schildkraut, New England Biolabs, Inc. |
| Applications： | in suitable host, produces protein modification methylase EagI in suitable host, produces protein restriction endonuclease EagI |
| Vector： | Construct size (kb): 7.30 |
| Insert： | DNA: genomic Insert lengths(kb): 2.90 Gene product: restriction endonuclease EagI hsdM Target Gene: modification methylase EagI, restriction endonuclease EagI |
| Insert Size (kb)： | 2.900 |
| 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： | Shipped: xa0Original depositor-supplied purified DNA. Distributed in aliquots sufficient for transformation. |
| Comments： | Restriction digests of the clone give the following sizes (kb): PstI--4.5, 2.9; EcoRV--4.4, 1.5 (doublet): AvaI--4.1, 3.3; NotI--uncut. The insert contains the following restriction sites (approximate kb from the end closer to the ori): EcoRV--0.8, 2.4; ClaI--1.2, 2.2; SacI--1.6; PvuII--2.7. The vector is pBR322 modified such that the EcoRI site, the PvuII site, and the two DraI sites located outside of the bla gene have been replaced by NotI sites. Distributed in aliquots sufficient for transformation. |
| References： | Brooks JE, Sznyter LA. Method for producing the EagI restriction endonuclease and methylase. US Patent 4,996,151 dated Feb 26 1991 |
| 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. |