GoldBio/RR1 Chemically Competent E. coli Cells/5 x 50 μl/CC-113-5x50

GoldBio’s RR1 chemically competent E. coli cells are suitable for high-efficiency transformation in a wide variety of applications such as cloning and sub-cloning. E. coli RR1 is a recA+ derivative of the HB101 strain and can be more useful than HB101 if a recA+ background is required.

Product SpecificationsCompetent cell type: Chemically competentDerivative of: RR1Species: E. coliFormat: TubesTransformation efficiency: ≥3 x 10⁷ cfu/μg pUC19 DNABlue/white screening: No

Storage/Handling: This product may be shipped on dry ice. RR1 Chemically Competent E. coli cells should be stored at -80°C, pUC19 Control DNA should be stored at -20°C and recovery medium should be stored at 4°C immediately upon arrival. When stored under the recommended conditions and handled correctly, these products should be stable for at least 1 year from the date of receipt.

Genotype

F- Lambda- araC14 leuB6(Am) DE(gpt-proA)62 lacY1 glnX44(AS) galK2(Oc) recA+ rpsL20(strR) xylA5 mtl-1 thiE1 hsdS20(rB-, mB-)

Reagents Needed for One Reaction

• RR1 chemically competent cells: 50 μl
• DNA (or pUC19 Control, 10 pg/μl): 1 μl
• Recovery medium: 1 ml

Quality ControlTransformation efficiency is tested by using the pUC19 control DNA supplied with the kit and using the protocol given below. Transformation efficiency should be ≥3 x 10⁷ CFU/μg pUC19 DNA. Untransformed cells are tested for appropriate antibiotic sensitivity.

General Guidelines

• 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.

Calculation of Transformation EfficiencyTransformation Efficiency (TE) is defined as the number of colony forming units (cfu) produced by transforming 1 μg of plasmid into a given volume of competent cells.

• TE = Colonies/μg/Dilution
  • Colonies = the number of colonies counted
  • μg = amount of DNA transformed in μg
  • Dilution = total dilution of the DNA before plating

Example: Transform 1 μl of (10 pg/μl) control plasmid into 25 μl of cells, add 975 μl of Recovery Medium. Dilute 10 μl of this in 990 μl of Recovery Medium and plate 50 μl. Count the colonies on the plate the next day. If you count 250 colonies, the TE is calculated as follows:Colonies = 250μg of DNA = 0.00001 Dilution = 10/1000 x 50/1000 = 0.0005 TE = 250/0.00001/0.0005 = 5.0 × 10¹⁰