Takara HST08 Premium Competent Cells Manual

E.coli Competent Cells HST08 Premium is a high-efficiency host E.coli HST08 Premium that has a high transformation efficiency and can be used for the preparation of methylated plasmids. It is also suitable for the cloning of long fragments of 10 kbp and above. When it is used with Takara DNA Ligation Kit LONG (Takara Code: D6024), it works well. pUC series plasmids, BAC libraries, and other conversions can be used. β-galactosidase α-complementation can be used to add X-gal for blue-white screening to select positive clones.


Brand
E.coli
Category
Other
Document type
User Manual
Language
Chinese
Pages
1
File format
PDF
File size
246 KB
Updated
30 September, 2023
Model
HST08
MD5 checksum
5E3ABEA4B27F9EB3E9B33F0CC66F51E5

About this manual

The HST08 Premium competent cells are a high‑efficiency strain supplied by Takara for cloning applications, especially when target DNA is present at low concentrations. The product includes 100 µl aliquots (10 tubes) and a control pUC19 DNA (0.1 ng) for reference.

The manual details thawing, mixing with up to 10 ng of DNA, a 30‑minute ice incubation, a 45‑60 second heat‑shock at 42 °C, and recovery in SOC medium. It also lists storage at –80 °C, recommended tube types, and precautions to maintain transformation efficiency. This manual is written in Chinese.

What's inside

  • Product Description
  • Genotype
  • Packaging
  • Storage Conditions
  • Transformation Procedure
  • Precautions
  • SOC Medium Composition

Specifications

Packaging100 µl × 10 tubes
Control DNApUC19, 0.1 ng per tube (10 × 1)
Cell Concentration1–2 × 10³ cells/µl
Typical Transformation Efficiency> 1 × 10⁸ transformants per µg pUC19
Heat‑Shock Condition42 °C for 45–60 seconds
SOC Medium Composition2% Bacto tryptone, 0.5% Bacto yeast extract, 10 mM NaCl, 2.5 mM K₂HPO₄, 10 mM MgSO₄, 10 mM MgCl₂, 20 mM Glucose

Frequently asked questions

What heat‑shock time and temperature are recommended for transformation?

After adding DNA, incubate the mixture at 42 °C for 45–60 seconds.

What is the composition of the SOC recovery medium?

SOC contains 2% Bacto tryptone, 0.5% Bacto yeast extract, 10 mM NaCl, 2.5 mM K₂HPO₄, 10 mM MgSO₄, 10 mM MgCl₂, and 20 mM glucose.

What transformation efficiency can be expected with pUC19 DNA?

More than 1 × 10⁸ transformants per µg of pUC19 DNA are typically obtained.

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