AGL1 electro competent cells (MOFY-0822-FY535)


Cat: MOFY-0822-FY535
Certificate of Analysis Lookup
To download a Certificate of Analysis, please enter a lot number in the search box below. Note: Certificate of Analysis not available for kit components.
Lot Number

Size:
 Inquiry
  • Product Details

Specifications

DescriptionThe AGL1 strain is C58, RecA type background, and the nuclear gene contains screening tags-rifampicin resistance gene rif and carbenicillin resistance gene carb, in order to facilitate the transformation operation, this strain carries a succinine type without self-transport function Ti plasmid pTiBo542DT-DNA, AGL1 strain is suitable for transgenic operation of rice, Arabidopsis, poplar and other plants.
Gene TypesC58 RecA (rifR/carbR) Ti pTiBo542DT-DNA Succinamopine
Size50 µL/vial
QC resultTransformation efficiency of pCAMBIA2301 plasmid (size:11633 bp) detection:>105 cfu/μg DNA; Transformation efficiency of pCAMBIA2301-ZH plasmid (size:40 kb) detection:>5×103 cfu/μg DNA.
Note1. When the plasmid is added, the volume should not be greater than 1/10 of the competent volume; if the plasmid is impure or there is organic pollution such as ethanol, the transformation efficiency will drop sharply; if the plasmid is doubled, the transformation efficiency will drop by an order of magnitude.
2. Be gentle when mixing plasmids. Transforming high concentrations of plasmids can correspondingly reduce the amount of bacteria that are ultimately used for plating.
3. When the density of positive clones on the plate is too large, due to insufficient nutrition, the growth of positive clones will slow down and the colonies will become smaller. In order to obtain large colonies, the amount of plasmid should be reduced.
4. The concentration of rifampicin should not be higher than 25 μg/ml. Too high concentration of rifampicin is not conducive to the growth of Agrobacterium and will reduce its growth rate and transformation efficiency. The plate used by our company to calculate the transformation efficiency only contains 50 μg/ml kan. If the plate used contains 20 μg/ml rif, the transformation efficiency will be reduced to 1/2.
5. The purpose of adding rifampicin to the medium is to prevent the growth of miscellaneous bacteria and screen Agrobacterium; adding Ti plasmid to screen antibiotics according to the resistance of the strain used can prevent the loss of Ti plasmid, but Ti plasmid screening antibiotics is not conducive to the transgenic operation of Agrobacterium. Therefore, these antibiotics are generally not considered when culturing Agrobacterium, and the probability of Ti plasmid loss is extremely low (can be ignored).

Properties

ShippingDry ice
StorageStore at -80 °C
Handling AdviceImmediately upon receipt, cells were transferred from dry ice to -80°C refrigerator.
Related Products
MOFY-0822-FY536AGL1(pSoup) competent cells (MOFY-0822-FY536)
MOFY-0822-FY537AGL1 competent cells (MOFY-0822-FY537)
For Research Use Only | Not For Clinical Use.
Online Inquiry