GreenGate 2.0 (GG2.0) expands the current GreenGate (GG)features set. GG2.0 offers an expanded repertoire of overhangs subdividing the existing GG A to E modules into 14 sub-modules. These modules can be cloned in a unique Universal entry vector to generate Level 0 entry clones. Up to 12 Level 0 clones can be assembled in one GG2.0 transcriptional unit compared to six for GG. Whereas GG only allowed the combination of two TUs to form a multi-gene Level 2 assembly, GG2.0 leverages GreenBraiding for the parallel, iterative assembly of a limitless number of TUs in Level 2 assemblies.</p
<p>A) Type IIS restriction endonucleases, such as <i>Bsa</i>I, have a distinct, non-palindromic reco...
During the last 30 years, Genomics has been revolutionized by the development of first- and second-g...
Assembling composite DNA modules from custom DNA parts has become routine due to recent technologica...
Molecular cloning is a crucial technique in genetic engineering that enables the precise design of s...
Molecular cloning is a crucial technique in genetic engineering that enables the precise design of s...
Molecular cloning is a crucial technique in genetic engineering that enables the precise design of s...
Molecular cloning is a crucial technique in genetic engineering that enables the precise design of s...
<p>A) The GreenGate cloning system uses six different types of pUC19 based entry vectors into which ...
GG2.0 introduces six new overhangs (in grey) that subdivide the existing GG A to E modules into 14 s...
Building expression constructs for transgenesis is one of the fundamental day-to-day tasks in modern...
(A) Key components and cloning sites of the GreenBraid destination plasmids (pGB). The PaqCI/AarI an...
The continual demand for specialized molecular cloning techniques that suit a broad range of applica...
<div><p>Standardized DNA assembly strategies facilitate the generation of multigene constructs from ...
<p>The NGA50 length (<b>A</b>, in kilobases) and the number of mis-assemblies (<b>B</b>, combining l...
<p>(a) Scheme of entry clone generation in pJOG130. Either PCR products flanked by <i>Bsa</i>I restr...
<p>A) Type IIS restriction endonucleases, such as <i>Bsa</i>I, have a distinct, non-palindromic reco...
During the last 30 years, Genomics has been revolutionized by the development of first- and second-g...
Assembling composite DNA modules from custom DNA parts has become routine due to recent technologica...
Molecular cloning is a crucial technique in genetic engineering that enables the precise design of s...
Molecular cloning is a crucial technique in genetic engineering that enables the precise design of s...
Molecular cloning is a crucial technique in genetic engineering that enables the precise design of s...
Molecular cloning is a crucial technique in genetic engineering that enables the precise design of s...
<p>A) The GreenGate cloning system uses six different types of pUC19 based entry vectors into which ...
GG2.0 introduces six new overhangs (in grey) that subdivide the existing GG A to E modules into 14 s...
Building expression constructs for transgenesis is one of the fundamental day-to-day tasks in modern...
(A) Key components and cloning sites of the GreenBraid destination plasmids (pGB). The PaqCI/AarI an...
The continual demand for specialized molecular cloning techniques that suit a broad range of applica...
<div><p>Standardized DNA assembly strategies facilitate the generation of multigene constructs from ...
<p>The NGA50 length (<b>A</b>, in kilobases) and the number of mis-assemblies (<b>B</b>, combining l...
<p>(a) Scheme of entry clone generation in pJOG130. Either PCR products flanked by <i>Bsa</i>I restr...
<p>A) Type IIS restriction endonucleases, such as <i>Bsa</i>I, have a distinct, non-palindromic reco...
During the last 30 years, Genomics has been revolutionized by the development of first- and second-g...
Assembling composite DNA modules from custom DNA parts has become routine due to recent technologica...