Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.
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グレード
Molecular Biology
for molecular biology
フォーム
suspension
輸送温度
dry ice
保管温度
−70°C
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詳細
Thunderbolt GC10 electrocompetent E. coli have a very high transformation efficiency of >1x1010 cfu/μg when transformed with non-saturating amounts of pUC19 plasmid DNA. They are comparable to DH10β strain.
アプリケーション
Suitable for recovery of high quality plasmid DNA and generation of cDNA libraries from plasmid-based vectors
特徴および利点
- Ensures recovery of stable, high quality plasmid DNA as well as methylated DNA
- Renders protection to clonal stocks from T1 and T5 bacteriophage contamination
- Allows for β-galactosidase α-complementation for blue/white screening
- Guaranteed high transformation efficiency
- Convenient 80 μL or 100 μL aliquots
構成
- Thunderbolt GC10 electrocompetent cells, 5 X 80 μL or 5 X 100 μL (T7074)
- pUC 19 control DNA (10 ng/μL), 10 μL (D2567)
原理
Thunderbolt GC10 electrocompetent E. coli is K strain bacteria that contain mutations in recA1 and endA1 genes. These mutations aid in minimizing recombination and ensuring plasmid stability. This strain also contains tonA genotype that confers resistance to lytic bacteriophages such as T1 and T5. The host restriction systems are eliminated to allow the cloning of methylated DNA.
法的情報
GC10 is a trademark of GeneChoice, Inc.
Thunderbolt is a trademark of GeneChoice, Inc.
関連製品
製品番号
詳細
価格
保管分類コード
12 - Non Combustible Liquids
WGK
WGK 1
引火点(°F)
Not applicable
引火点(℃)
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Jan Code
T7699-5X100UL:
T7699-5X80UL:
T7699-BULK:
T7699-VAR:
Dana G Mordue et al.
Molecular microbiology, 63(2), 482-496 (2006-12-15)
The apicomplexan parasite Toxoplasma gondii is able to suppress nitric oxide production in activated macrophages. A screen of over 6000 T. gondii insertional mutants identified two clones, which were consistently unable to suppress nitric oxide production from activated macrophages. One
Jeffrey Sabina et al.
The Journal of biological chemistry, 284(43), 29635-29643 (2009-09-02)
Efficient uptake of glucose is especially critical to Saccharomyces cerevisiae because its preference to ferment this carbon source demands high flux through glycolysis. Glucose induces expression of HXT genes encoding hexose transporters through a signal generated by the Snf3 and
W Florian Fricke et al.
Journal of bacteriology, 190(20), 6779-6794 (2008-08-19)
The increasing occurrence of multidrug-resistant pathogens of clinical and agricultural importance is a global public health concern. While antimicrobial use in human and veterinary medicine is known to contribute to the dissemination of antimicrobial resistance, the impact of microbial communities
D Lee Taylor et al.
Molecular ecology resources, 8(4), 742-752 (2008-07-01)
High throughput sequencing methods are widely used in analyses of microbial diversity, but are generally applied to small numbers of samples, which precludes characterization of patterns of microbial diversity across space and time. We have designed a primer-tagging approach that
Plasmids of Escherichia coli as cloning vectors.
F Bolivar et al.
Methods in enzymology, 68, 245-267 (1979-01-01)
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What is the Department of Transportation shipping information for this product?
1 回答-
役に立ちましたか？
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Are home-made competent cells as efficient at transformation as purchased cells?
1 回答-
They can be, depending on the technique used, the expected transformation efficiency and how the cells are handled. For special applications, competent cells prepared in-house using standard methods may not provide the efficiency you need.
役に立ちましたか？
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Can I re-freeze the vial if I do not use the entire aliquot of competent cells?
1 回答-
Re-freezing competent cells will result in a decrease in their transformation efficiency. If the cells are frozen first in a dry ice / ethanol bath before placement in the -80C freezer, the loss will be about two-fold. If placed directly in the -80C freezer, the loss in transformation efficiency is about five to ten-fold.
役に立ちましたか？
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How should I thaw the competent cells?
1 回答-
Competent cells should be thawed on ice. The transformation efficiency is dependent on the proper handling of the cells (maintaining cold temperature until transformation).
役に立ちましたか？
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Are all competent cells suitable for both plasmid production and protein expression?
1 回答-
No. Most strains of competent cells are suitable for producing plasmid DNA that will be used to transfect insect or mammalian cells for expression of the protein. The BL21 competent cell strains have special traits enabling protein expression in bacteria.
役に立ちましたか？
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What are important considerations when performing bacterial transformation?
1 回答-
Things to consider when planning bacterial transformation:DNA impuritiesSource of DNAAmount of DNA usedStorage and handling of the competent cells
役に立ちましたか？
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Competent cells were left on ice overnight - can they still be used?
1 回答-
Competent cells left on ice, or allowed to come to room temperature slowly will suffer a dramatic loss in transformation efficiency. We recommend thawing a new aliquot of competent cells.
役に立ちましたか？
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Can I grow more competent cells from the stock I purchased?
1 回答-
Generally, no, because the future generations of cells lose their competency.
役に立ちましたか？
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Can I store the competent cells in the -20C?
1 回答-
No. Competent cells should not be stored at -20C for any length of time. The cells suffer a dramatic drop in transformation efficiency when stored higher than -80C.
役に立ちましたか？
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What DNA purity do I need for use in transformation?
1 回答-
The DNA used should be high quality - free from phenol, proteins, detergents, and ethanol. Dissolve the DNA in sterile water or 0.5x TE buffer (5 mM Tris-HCl, 0.5 mM EDTA).
役に立ちましたか？
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