JM109 receptive cells produced by our company are receptive cells obtained by special processing of Escherichia coli JM109 strain, which can be used for chemical transformation of DNA. Using pUC19 plasmid detection, the conversion efficiency can reach 108, and the conversion efficiency does not change when stored at -70℃ for several months.

Genotype: recA supE44 endA1 hsdR17 gyrA96relA1 thi Δ(lac-proAB) F '[traD36 proAB+ lacIq lacZ δM15]

Characteristics: An amber inhibited F 'recombinant defective strain. It supports the growth of M13 phage vector and has modification effect on transfected DNA, but has no restriction effect. The F 'in this strain carries lacZΔM15, which enables alpha-complementation with the amino end of β-galactosidase encoded in λZAP and can be used for blue-white spot screening.

Operation method: (The following steps are aseptic operation)

1. Put the receptive cells on ice to melt. The following experiment takes the 100μL receptive cells as an example.

2. Add the target DNA to be transformed into the receptive cell suspension, and pay attention to the volume of the target DNA not exceeding one-tenth of the volume of the receptive cell suspension, gently rotate the centrifuge tube to mix the contents, and place it in an ice bath for 30min.

3. Place the centrifuge tube in a water bath at 42 ° C for 60-90s, and then quickly transfer to the ice bath for 2-3min. Be careful not to shake the centrifuge tube.

4. 500μL sterile and non-resistant SOC or LB medium was added into the centrifuge tube and cultured for 1h by oscillating at 180rpm at 37℃. The aim is to make the relative resistance marker genes expressed on the plasmid, so as to revive the bacteria.

5. Appropriate amount of transformed receptive cells were coated with SOC or LB plates containing corresponding antibiotics and cultured invert at 37℃ for 12-16h. The amount of coating can be adjusted according to the specific experiment, such as the total amount of converted DNA is more, the conversion product coating plate can be about 100μL; On the other hand, if the total amount of converted DNA is small, 200-300μL of conversion product coating is preferable. Excessive bacterial fluid can inhibit bacterial growth. If few clones are expected, part of the culture solution can be removed by centrifugation, and the bacteria can be suspended and coated on a plate. The remaining bacterial solution can be stored at 4℃, and if the number of transformed colonies is too low the next day, the remaining bacterial solution can be coated with a new plate.

Note:

1. The receptive cells should be stored at -70℃, can not be frozen and thawed repeatedly, otherwise its conversion efficiency will be reduced.

2. The experiment should be strictly aseptic operation, to prevent the contamination of other DNA, to avoid the impact on future screening and identification.

3. During conversion, the conversion efficiency is proportional to the concentration of foreign DNA within a certain range, but when the amount of foreign DNA added is too large or the volume is too large, the conversion efficiency will be reduced. At the time of transformation, the DNA volume is less than one-tenth of the volume of the receptive cell.

4. Calculation of conversion rate: conversion rate = total number of colonies generated/total amount of pavement DNA

5. In order to prevent the conversion experiment is unsuccessful, some of the connected products can be retained to re-transform, and the loss will be minimized.

Note：Product information may be optimized and upgraded. Please refer to the actual label information for accuracy.