Super competent Cell Preparation Kit
Reagent
Code: #246912
blur_circular Chemical Specifications
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Storage & Handling
Storage
-20°C
description Product Description
Used in molecular biology for highly efficient transformation of plasmid DNA into bacterial cells. Enables rapid cloning and protein expression workflows by allowing even low-copy plasmids to be transformed with high success rates. Ideal for library construction, site-directed mutagenesis, and recombinant protein production. Requires no heat shock or lengthy incubations—compatible with standard laboratory protocols for fast and reliable results.
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| Test Parameter | Specification |
|---|---|
| Performance test | PASS |
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Super Competent Cell Preparation Kit
Product Introduction
This kit is used for rapid preparation of high-transformation-efficiencyEscherichia colicompetent cells. The kit includes specialized bacterial culture medium and preparation reagents.
The competent cell preparation process can be completed in up to 40 min. Verified transformation efficiency can reach 108–109cfu/μg plasmid.
Product Packing List
| Product Code | Component | 100T | 200T |
|---|---|---|---|
| 246912.1 | Escherichia coliculture medium | 150 mL | 300 mL |
| 246912.2 | Preparation Reagent A | 50 mL | 100 mL |
| 246912.3 | Preparation Reagent B | 1 mL | 2 mL |
| 246912.m | Instructions | 1 copy | 1 copy |
Quality Standards and Safety Information
| Raw Material or Packaging Name | Quality Standard | Main Toxicity |
|---|---|---|
| Bacterial culture medium | Sterile, enzyme-free | — |
| Reagent A | Sterile, enzyme-free | — |
| Reagent B | Sterile, enzyme-free | — |
Shipping and Storage Conditions
| Shipping | This product is shipped with ice packs. |
|---|---|
| Storage | Store Preparation Reagent A at -20°C and avoid repeated freezing and thawing. Store the bacterial culture medium and Preparation Reagent B at room temperature. |
Instructions for Use
Perform all experiments below under aseptic conditions. Perform the second-step reaction on ice, and pre-cool the centrifuge to 4°C in advance.
I. Obtain a Monoclonal Bacterial Culture
- Take 10 μL of preserved glycerol bacteria or another bacterial culture, add 1 mL bacterial culture medium, and incubate at 37°C and 220 rpm for 12 h.
- Take an appropriate amount of the bacterial culture and spread it on a non-antibiotic LB plate. Incubate inverted at 37°C for 10 h.
- Pick a single clone, add 1 mL bacterial culture medium, and incubate at 37°C and 220 rpm for 12 h to obtain the monoclonal bacterial culture.
II. Prepare Competent Cells
- Take 100 μL of the bacterial culture prepared above and add it to 50 mLE. coliculture medium. Culture at 18°C and 220 rpm for 14 h, until OD600is approximately 0.55.
- Let the culture stand on ice for 10 min.
- Transfer the culture to a centrifuge tube. Centrifuge at 4°C and 3500 rpm for 10 min to collect the bacterial cells. The centrifuge must be pre-cooled in advance.
- Discard the supernatant. Add 16 mL ice-cold Preparation Reagent A to resuspend the cells. Centrifuge at 4°C and 3500 rpm for 10 min.
- Discard the supernatant. Add 4 mL ice-cold, pre-cooled Preparation Reagent A to resuspend the cells. Add 300 μL Preparation Reagent B and mix gently.
- On ice, aliquot the solution into sterile, nuclease-free EP tubes at 100 μL per tube.
- Immediately place the tubes in liquid nitrogen for rapid freezing, then store at -80°C. Under normal conditions, transformation efficiency will not change significantly after 6 months.
Precautions
- This kit is suitable for mostEscherichia colistrains, such as DH5α, Top10, Trans1-T1, and BL21(DE3).
- For safety and health, wear a lab coat and disposable gloves when operating.
- This product is for research use only.
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