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

One Shot™ TOP10 Chemically Competent E. coli

TOP10 E. coli 의 transformation efficiency는 supercoiled DNA 1 micro;g 당 1 x 10e9 cfu로 고효율 클로닝과 plasmid 증식에 이상적입니다.자세히 알아보기
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카탈로그 번호수량
C40400642 x 50 μL
C40401011 x 50 μL
C40400321 x 50 μL
카탈로그 번호 C404006
제품 가격(KRW)
836,000
Precio exclusivo en nuestra web
Ends: 31-Dec-2025
879,000
할인액 43,000 (5%)
Each
카트에 추가하기
수량:
42 x 50 μL
제품 가격(KRW)
836,000
Precio exclusivo en nuestra web
Ends: 31-Dec-2025
879,000
할인액 43,000 (5%)
Each
카트에 추가하기
TOP10 E. coli 의 transformation efficiency는 supercoiled DNA 1 micro;g 당 1 x 10e9 cfu로 고효율 클로닝과 plasmid 증식에 이상적입니다. 이는 high-copy plasmid의 안정적인 복제를 가능하게 합니다. TOP10 세포의 유전자형은 DH10B™strain과 유사하며, 다음과 같은 특징을 제공합니다.
 
-hsdR-: PCR 증폭 산물 중 unmethylated DNA의 효율적인 transformation
-mcrA : Genomic DNA 중 methylated DNA의 효율적인 transformation
-lacZΔM15 : 재조합 클론의 blue/white 스크리닝
-endA1: Endonuclease I에 의한 비특이적 digestion 제거로 깨끗한 DNA 추출과 다음 분석 어플리케이션 결과가 향상됨
-recA1: 클론 DNA의 비특이적 재조합 발생이 감소됨
 
One Shot™ TOP10 Kit는 각 transformation 요구에 맞게 chemically competent 또는 electrocompetent E. coli 로 이용할 수 있습니다. TOP10 E. coli 는 high-throughput MultiShot™ 형식으로도 구매 가능합니다.
For Research Use Only. Not for use in diagnostic procedures.
사양
항생제 내성 박테리아Yes (Streptomycin)
블루/화이트 스크리닝Yes (lacZΔM15)
메틸화 DNA 클로닝Yes (mcrA)
불안정 DNA 클로닝No
에프에피솜 포함No
고처리량 호환성Low
플라스미드 품질 개선Yes (endA1)
플라스미드High Copy Plasmid
비메틸화 DNA 준비No
제품라인One Shot
제품 유형Chemically Competent Cells
수량42 x 50 μL
재조합 감소Yes (recA1)
배송 조건Dry Ice
T1 Phage - 저항성(tonA)No
형질전환 효율 수준High Efficiency (>1 x 109 cfu/μg)
형식Tube
E. coli (K12)
Unit SizeEach
구성 및 보관
• One Shot TOP10 Chemically Competent E. coli (42 x 50 μL)
Store Competent Cells at –80°C.

• pUC19 DNA (50 μL at 10 pg/μL)
Store pUC19 DNA at –20°C.

• S.O.C. medium (6 mL)
Store S.O.C. Medium at 4°C or room temperature.

자주 묻는 질문(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.

인용 및 참조 문헌 (3)

인용 및 참조 문헌
Abstract
Cloning and Characterization of a Cryptic Haloacid Dehalogenase from Burkholderia cepacia MBA4
Authors:J. Tsang and L. Sam
Journal:J Bacteriol
PubMed ID:10498712
Burkholderia cepacia MBA4 has been shown to produce a single dehalogenase batch culture.Moreover, other cryptic dehalogenases were also detected when the cells were grown in continuousculture. In this paper, we report the cloning and characterization of one of the cryptic dehalogenases inMBA4. This cryptic haloacid dehalogenase, designated Chd1, was expressed ... More
Endogenous heparan sulfate and heparin modulate bone morphogenetic protein-4 signaling and activity.
Authors:Khan SA, Nelson MS, Pan C, Gaffney PM, Gupta P,
Journal:Am J Physiol Cell Physiol
PubMed ID:18385288
Bone morphogenetic proteins (BMPs) and their endogenous antagonists are important for brain and bone development and tumor initiation and progression. Heparan sulfate (HS) proteoglycans (HSPG) modulate the activities of BMPs and their antagonists. How glycosaminoglycans (GAGs) influence BMP activity in various malignancies and in inherited abnormalities of GAG metabolism, and ... More
Methyl-CpG binding domain protein 2 represses transcription from hypermethylated pi-class glutathione S-transferase gene promoters in hepatocellular carcinoma cells.
Authors: Bakker Jila; Lin Xiaohui; Nelson William G;
Journal:J Biol Chem
PubMed ID:11960994
During the pathogenesis of human hepatocellular carcinoma (HCC), the CpG island encompassing the pi-class glutathione S-transferase gene (GSTP1) becomes hypermethylated. Repression of transcription accompanying CpG island hypermethylation has been proposed to be mediated by methyl-CpG binding domain (MBD) proteins. We report here that inhibition of transcription from hypermethylated GSTP1 promoters ... More