AGL1 Electroporation Competent Cell

ACC-113

AGL1 Electroporation Competent Cell

The genotype of AGL1 Electroporation Competent Cell is C58 RecA (rif R/carb R) Ti pTiBo542DT-DNA (Strep R) Succinamopine. Background of AGL1 strain is C58, RecA-type. It contains rifampicin resistant gene (rif) and the carbenicillin resistance gene (carb) as screening label. AGL1 carries amber basic Ti plasmid pAGL1 (pTiBo542DT-DNA) to facilitate transformation. Ti plasmid pAGL1 (pTiBo542DT-DNA) contains vir gene, which is essential for insertion of T-DNA into plant genome. Ti plasmid pAGL1 (pTiBo542DT-DNA) is disabled to transfer its own T-DNA but enabled to transfer foreign binary vector T-DNA. pAGL1 (pTiBo542DT-DNA) Ti plasmid contains streptomycin resistance gene. AGL1 Electroporation Competent Cell is particularly suitable for large plasmid transformation.

AGL1 Electroporation Competent Cell is suitable for transgenic operations of rice, Arabidopsis, poplar and other plants.

1. Volume of DNA from ligation mix should not exceed 1/10 of the cell mixture; DNA for transformation should be purified and free of organic substances such as ethanol.
2. Do not pipette or vortex cells.
3. Plating volume can be adjusted accordingly.
4. Please avoid excessive use of rifampicin. Maximum concentration of rifampicin in selection is 25 μg/mL.

Store at - 80 °C for 12 months.

AGL1 Electroporation: 50 μL/tube * 10 tube/50 tube.

Transformation efficiency of AGL1 Electroporation Competent Cell using pCAMBIA2301 plasmid with 50 μg/mL kan is >10^5 cfu/μg DNA. Transformation efficiency is reduced to half when the plate contains 50 μg/mL kan and 20 μg/mL rif.