One Shot™ TOP10 Electrocomp™ E. coli
One Shot&trade; TOP10 Electrocomp&trade; <i>E. coli</i>
Invitrogen™

One Shot™ TOP10 Electrocomp™ E. coli

One Shot™ TOP10 Electrocomp™ E. coli は、1 x 1010詳細を見る
製品番号(カタログ番号)数量
C40405011 x 50 μL, 10 Reactions
C40405221 x 50 μL, 20 Reactions
製品番号(カタログ番号) C404050
価格(JPY)
53,500
Each
お問い合わせください ›
数量:
11 x 50 μL, 10 Reactions
One Shot™ TOP10 Electrocomp™ E. coli は、1 x 1010 cfu/ µgスーパーコイルDNAの形質転換効率で提供され、高効率クローニングやプラスミド増殖に最適です。コピー数の多いプラスミドの安定した複製が可能です。TOP10細胞のジェノタイプは、DH10B™株のジェノタイプに似ており、以下の特徴を備えています。

hsdR:PCR増幅から非メチル化DNAを効率的に形質転換
mcrA:ゲノム調製からメチル化DNAを効率的に形質転換
lacZΔM15:組換えクローンの青/白をカラースクリーニング
endA1:DNAをよりクリーンに調製—エンドヌクレアーゼIによる非特異的消化の除去によって、下流アプリケーションでの結果を改善
recA1:クローンDNA中の非特異的な組換えの発生を低減

キットのオプション
One Shot™ TOP10キットは、ケミカルコンピテントまたはエレクトロコンピテントE. coli のいずれかと一緒に使用して、特定の形質転換ニーズに合わせることができます。TOP10 E. coli は、ハイスループットのMultiShot™フォーマットでもご利用いただけます。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
抗生物質耐性菌Yes (Streptomycin)
青/白スクリーニング
メチル化DNAのクローニング
不安定DNAのクローニング不安定なDNAのクローニングには不適
F'エピソームを含むNo
高スループット適合性ハイスループット非対応(手動)
プラスミドの品質を向上
プラスミドプラスミド 20 kb>に使用できます。
非メチル化DNAの調製非メチル化DNAの調製には適していません
製品ラインOne Shot
製品タイプ大腸菌
数量11 x 50 μL, 10 Reactions
組換えを抑制
出荷条件ドライアイス
T1ファージ-耐性(tonA)No
形質転換効率レベル高効率(> 10^9 cfu⁄µg)
フォーマットOne Shot
E. coli
Unit SizeEach
組成および保存条件
超低温フリーザー(-68~-85℃)に保存。

よくあるご質問(FAQ)

What is the difference between TOP10 and TOP10F' cells?

The only difference between TOP10 and TOP10F' cells is that the latter contain the F' episome that carries the tetracycline resistance gene and allows isolation of single-stranded DNA from vectors that have an f1 origin of replication. The F' episome also carries the lacIq repressor for inducible expression from trc, tac, and lac promoters using IPTG. TOP10F' cells require IPTG induction for blue/white screening.

I am trying to clone an insert that is supposedly pretty toxic. I used DH5? and TOP10 cells for the transformation and got no colonies on the plate. Do you have any suggestions for me?

If the insert is potentially toxic to the host cells, here are some suggestions that you can try:

- After transforming TOP10 or DH5? cells, incubate at 25-30°C instead of 37°C. This will slow down the growth and will increase the chances of cloning a potentially toxic insert.
- Try using TOP10F' cells for the transformation, but do not add IPTG to the plates. These cells carry the lacIq repressor that represses expression from the lac promoter and so allows cloning of toxic genes. Keep in mind that in the absence of IPTG, blue-white screening cannot be performed.
- Try using Stbl2 cells for the transformation.

Can I directly clone, propagate and express in BL21 without using TOP10?

It is imperative that a cloning strain such as TOP10 be used for characterization of the plasmid, propagation, and maintenance. BL21 cells are wild-type for endA and recA, which could result in poor miniprep quality and a greater chance of plasmid rearrangements due to recombination. In addition, BL21 cells contain the T7 RNA polymerase gene which is expressed at low levels even in the absence of inducer. If the gene is toxic to E. coli, plasmid instability and/or cell death can result.

I need to clone unmethylated DNA from a PCR reaction using a strain that has the hsdRMS mutation to avoid restriction after transformation. Is TOP10 suitable for my purposes?

Yes, TOP10 has the hsdRMS mutation, so this strain can be used to clone DNA from PCR reactions and other non-methylated sources. hsdRMS is a mutation in the system that E. coli uses to recognize foreign DNA. There are two parts to this system, methylation and restriction. E. coli methylate DNA at certain sequences, and if the DNA is not methylated at these sequences it will be recognized as foreign and restricted. Thus, if unmethylated DNA is transformed into E.coli that does not carry the hsdRMS genotype, it is recognized as foreign and enzymatically degraded.

Are TOP10 cells lacIq+ (plus) or lacIq- (minus)? That is, do they produce the lambda lacIq repressor protein?

TOP10 cells are lacIq- (minus). They do not have the lacIq gene and therefore do not produce the lacIq repressor protein. lacIq is most commonly found on an F' episome, and therefore is present in TOP10F', JM101, JM109, and NM522 strains.

引用および参考文献 (1)

引用および参考文献
Abstract
High throughput immuno-screening of cDNA expression libraries produced by in vitro recombination; exploring the Plasmodium falciparum proteome.
Authors:Kordai Sowa MP, Sharling L, Humphreys G, Cavanagh DR, Gregory WF, Fenn K, Creasey AM, Arnot DE,
Journal:Mol Biochem Parasitol
PubMed ID:14698438
Improved Plasmodium falciparum cDNA expression libraries were constructed by combining mRNA oligo-capping with in vitro recombination and directional cloning of cDNA inserts into a plasmid vector that expresses sequences as thioredoxin fusion proteins. A novel procedure has also been developed for the rapid identification of seropositive clones on high-density filters, ... More