TG1 Phage Display Electrocompetent Cells

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Description

GoldBio’s TG1 Phage Display Electrocompetent E. coli cells are suitable for protein expression and preparation of antibody or peptide phage display libraries. TG1 Phage Display cells have ≥1 x 109 cfu/µg efficiency with electroporation and have Amber suppressor strain (supE).

Reagents Needed for One Reaction

  • TG1 Phage Display electrocompetent cells: 25 µL
  • DNA (or pUC19 Control, 500 pg/µL): 0.2 µL
  • Recovery medium: 1 mL

Kit Components

  • Competent Cells
  • 1 x 12 mL Recovery Media
  • 1 x 10 µL Control Plasmid (pUC19 Control, 500 pg/µL)

Storage/Handling

This product may be shipped on dry ice. TG1 Phage Display Electrocompetent 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.

Genomic Features

  • ≥1 x 109 cfu/µg efficiency with electroporation.
  • Amber suppressor strain (supE)

Genotype

F’ [traD36 proAB+ lacIq lacZΔM15] supE thi-1 Δ(mcrB-hsdSM)5(rK-mK-) Δ(lac-proAB)

Quality Control

Transformation efficiency is tested by using the pUC19 control DNA supplied with the kit and using the protocol given below. Transformation efficiency should be ≥1 x 109 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.

Note: A high-voltage electroporation apparatus capable of generating field strengths of 16 kV/cm is required.

Calculation of Transformation Efficiency

Transformation 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 = 250
    µg of DNA = 0.00001
    Dilution = 10/1000 x 50/1000 = 0.0005
    TE = 250/0.00001/0.0005 = 5.0 × 1010

pUC Plasmid Vector

TG1 Phage Display Electrocompetent Cells

View Sizes & Pricing

Catalog Number:
CC-205-5x100
CAS Number:
$194.00 $155.00

Availability:
In Stock
Shipping:
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    Description

    GoldBio’s TG1 Phage Display Electrocompetent E. coli cells are suitable for protein expression and preparation of antibody or peptide phage display libraries. TG1 Phage Display cells have ≥1 x 109 cfu/µg efficiency with electroporation and have Amber suppressor strain (supE).

    Reagents Needed for One Reaction

    • TG1 Phage Display electrocompetent cells: 25 µL
    • DNA (or pUC19 Control, 500 pg/µL): 0.2 µL
    • Recovery medium: 1 mL

    Kit Components

    • Competent Cells
    • 1 x 12 mL Recovery Media
    • 1 x 10 µL Control Plasmid (pUC19 Control, 500 pg/µL)

    Storage/Handling

    This product may be shipped on dry ice. TG1 Phage Display Electrocompetent 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.

    Genomic Features

    • ≥1 x 109 cfu/µg efficiency with electroporation.
    • Amber suppressor strain (supE)

    Genotype

    F’ [traD36 proAB+ lacIq lacZΔM15] supE thi-1 Δ(mcrB-hsdSM)5(rK-mK-) Δ(lac-proAB)

    Quality Control

    Transformation efficiency is tested by using the pUC19 control DNA supplied with the kit and using the protocol given below. Transformation efficiency should be ≥1 x 109 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.

    Note: A high-voltage electroporation apparatus capable of generating field strengths of 16 kV/cm is required.

    Calculation of Transformation Efficiency

    Transformation 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 = 250
      µg of DNA = 0.00001
      Dilution = 10/1000 x 50/1000 = 0.0005
      TE = 250/0.00001/0.0005 = 5.0 × 1010

    pUC Plasmid Vector

    Product Specifications

    Catalog ID: CC-205
    Storage/handling: Store Competent Cells at -80°C.

    CITATIONS

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