GoldBio/DH5-alpha Chemically Competent E. coli Cells/10 x 50 μL/CC-101-10x50

GoldBio’s DH5-alpha Chemically Competent E. coli cells are suitable for high efficiency transformation in a wide variety of routine applications such as plasmid isolation, cloning, and subcloning.

Product SpecificationsCompetent cell type: Chemically CompetentDerivative of: DH5-alphaSpecies: E. coliTransformation efficiency: ≥5 x 10⁶ cfu/μg pUC19 DNABlue/white screening: Yes

Storage/Handling: This product may be shipped on dry ice. DH5-alpha 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.

GenotypeΦ80 Δ(lacZ)M15 fhuA2 Δ(argF-lacZ)U169 phoA glnV44 gyrA96 recA1 relA1 endA1 thi-1hsdR17

Reagents Needed for One Reaction

• DH5-alpha 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 ≥5 x 10⁶ 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