Transfected Stable Cell Lines
Reliable | High-Performance | Wide Rage
Precision reporter, kinase, immune receptor, biosimilar, Cas9, and knockout stable cell lines for diverse applications.
Cat. No. : EMNT2013
| Cat. No. | EMNT2013 |
| Description | Lambda Terminase is an endonuclease encoded by bacteriophage lambda that recognizes and cleaves DNA at cos sites, generating 5′ overhangs of 12 bases in length.3 Since the 12-base cos site sequence is rare, the sizes of inserts in BAC, fosmid, or cosmid clones can be rapidly determined.4 Epicentre"s Lambda Terminase is highly purified to provide reproducible cleavage with minimum nonspecific nicking activity. A typical digestion requires only 1 unit of Lambda Terminase for each microgram of DNA. |
| Concentration | 2000 units/ml |
| Applications | Rapid sizing of BAC, fosmid, or cosmid clones. Generation of restriction maps of BAC, cosmid, or fosmid clone inserts.1 Linearization of cos site-containing clones for in vitro packaging. Specific cleavage of chromosomal DNA for physical mapping.2 |
| Size | 50 units; 200 units |
| Unit Definition | One unit of Lambda Terminase linearizes up to 70% of 1 μg of the cosmid DNA vector pHC79 in 60 minutes at room temperature under standard assay conditions. |
| Storage | 50% glycerol containing 50 mM Tris-HCl (pH 7.5), 0.1 M NaCl, 0.1 mM EDTA, 1 mM DTT, and 0.1% Triton® X-100. |
A: The Lambda Terminase cutting rate at the 5' hydroxyl end is 20 times slower than at the 5' phosphate end.
A: Lambda exonuclease activity in different buffers is as follows: NEBuffer 1: 15%; NEBuffer 2: 40%; NEBuffer 3: 10%; NEBuffer 4: 40%; CutSmart: 50%; Nuclease I Reaction Buffer: 100%; Thermopol Reaction Buffer: 100%.
A: Unlike Lambda exonuclease, T5 exonuclease can degrade gapped circular dsDNA. T5 exonuclease can also act on ssDNA, which Lambda exonuclease cannot.
A: No, the Lambda Terminase cutting rate for single-stranded DNA is 100 times slower than for double-stranded DNA.
A: Lambda Restriction Enzyme can function in rCutSmart Buffer. To assess its functional activity percentage in rCutSmart, as well as the activity percentages of other DNA modifying enzymes in the cloning workflow, please refer to the following data.
A: Reaction buffer system: 67 mM Glycine-KOH, 2.5 mM MgCl2, 50 μg/ml BSA.
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