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Gene Bio Systems

Trans109 Chemically Competent Cell

Trans109 Chemically Competent Cell

SKU:CD301-02

Regular price $46.00 USD
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Product Size

Genotype

endA1 recA1 gyrA96 thi-1 hsdR17 (rk-, mk+) relA1 supE44 D (lac-proAB) [F′traD36 proAB laqIqZΔM15]

Features

• High transformation efficiency: >108 cfu/μg ( pUC19 DNA).

• The lowest homologous recombination favorable for plasmid DNA preparation.

• Routine cloning.

• Blue/white selection.

Storge

at -70 °C for six months

Notes

Higher efficiency transformation can be achieved by transforming cells immediately following thawing.

Avoid repeated thawing.

Gentle handling is required for the entire procedure.


References:

Literature Journal IF Author Date Link
MAPK signaling pathway alters expression of midgut ALP and ABCC genes and causes resistance to Bacillus thuringiensis Cry1Ac toxin in diamondback moth PLoS Genetics 8.167 Zhaojiang Guo?? et al 2015 Apr The original link
Bacillus thuringiensis subsp. sichuansis strain MC28 produces a novel crystal protein with activity against Culex quinquefasciatus larvae World Journal of Microbiology and Biotechnology 1.262 Peng Guan, et al. State Key Laboratory of Hybrid R 2014 Apr The original link
Cloning and characterisation of a novel cry1H gene effective against lepidopterous larvae from a Bacillus thuringiensis strain Biocontrol Science and Technology 0.848 Yu Z, et al. Sichuan agricultural university 2015 The original link

LiteratureJournalIFAuthorDateLinkDown-regulation of a novel ABC transporter gene (Pxwhite) is associated with Cry1Ac resistance in the diamondback moth, Plutella xylostella (L.)Insect Biochemistry and Molecular Biology3.42Zhaojiang Guo?? et al2015 JanThe original linkCloning, expression, and characterization of a novel xylose reductase from Rhizopus oryzaeJournal of Basic Microbiology1.823M Zhang, et al.2015 FebThe original linkProduction of poly(3-hydroxypropionate) and poly(3-hydroxybutyrate-co-3-hydroxypropionate) from glucose by engineering Escherichia coli0De-Chuan Meng, et al.2015 AprThe original link

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