Fig. 1
From: Gateway-compatible vectors for functional analysis of proteins in cell type specific manner
Cloning procedure of the intermediate vectors. a The backbone of dpGreenBarT was modified with attR4/attR3 gateway cassette replaced by attR1/attR2 gateway cassette being flanked by two multi-cloning sites (MCS-1 and MCS-2). The resulting vector was named as pSWU001. Different fluorescent proteins (FPs) and cell-specific promoters (labelled as promoter) were sequentially introduced into MCS-2 and MCS-1 of pSWU001 respectively. The complete sequences for MCS-1 and MCS-2 are shown in b