intactgenomics/Ar.Qual ElectroCompetent Agrobacterium | ig™ | Intact Genomics/6x50µl/1273-12

Intact Genomics (ig^®) Ar.Qual Electrocompetent Agrobacterium cells are made from a specific strain of Rhizobium rhizogenes (formerly Agrobacterium rhizogenes), Agrobacterium rhizogenes (str R,Cam R) Ar Qual Ri (agropine type). Agrobacterium rhizogenes is a soil-borne gram-negative bacterium that can infect most dicotyledons, a few monocotyledons and some gymnosperms.  Ar.Qual Electrocompetent Agrobacterium are optimized for the highest transformation efficiencies and are useful for transgenic operations of corn, tobacco, tomato, citrus and other plants.  Ar.Qual Agrobacterium rhizogenes strain contains agrobacterium-type Ri plasmid and displays streptomycin and chloramphenicol resistance.

SpecificationsCompetent cell type: ElectrocompetentSpecies: R. rhizogenesStrain: Ar.QualFormat: TubesTransformation efficiency: ≥ 1 x 10⁷  cfu/µg pIG7-spe DNABlue/white screening: NoShipping condition: Dry ice

Reagents Needed for One ReactionAr.Qual ElectroCompetent Agrobacterium: 25 µlDNA (pIG7-spe, 500 pg/µl): 1 µlRecovery medium: 1 ml

StorageAr.Qual ElectroCompetent Agrobacterium: -80 ºCpIG7-spe control DNA: -20 ºCRecovery medium: 4 ºC

Quality ControlTransformation efficiency is tested by using the pIG7-spe control DNA supplied with the kit and using the protocol in this manual. Transformation efficiency should be ≥1 x 10⁷ CFU/µg pIG7-spe DNA. Untransformed cells are tested for appropriate antibiotic sensitivity.

General GuidelinesFollow these guidelines when using Ar.Qual ElectroCompetent Agrobacterium:

• Handle competent cells gently as they are highly sensitive to changes in temperature or mechanical lysis caused by pipetting.
• Thaw competent cells on ice, and transform cells immediately following thawing. After adding DNA, mix by tapping the tube gently. Do not mix cells by pipetting or vortexing.

Note: A high-voltage electroporation apparatus such as Bio-Rad Gene Pulser II #165-2105, capable of generating field strengths of 16 kV/cm is required.

 Calculation of Transformation EfficiencyTransformation Efficiency (TE) is defined as the number of colony forming units (cfu) produced by transforming 1µg of plasmid into a given volume of competent cells.TE = Colonies/µg/PlatedTransform 1 µl of (500 pg/µl) pIG7-spe control plasmid into 25 µl of cells, add 974 µl of Recovery Medium. Recover for 3 hours and plate 100 µl. Count the colonies on the plate in two days. If you count 500 colonies, the TE is calculated as follows:Colonies = 500µg of DNA = 0.0005Dilution = 100/1000 = 0.1TE = 500/.0005/.1 = 1×10⁷

Please note, all agrobacterial strains are not well studied for antibiotic resistance and there are many agrobacterial strains.  Therefore, it is the customer’s responsibility to make sure his/her vectors are compatible with the Agrobacterial strains if he/she uses an alternate antibiotic selection than spectinomycin-selection.1273-12 1273-36