TOPO™ TA Cloning™ Kit, Dual Promoter, with One Shot™ TOP10 chemically competent E. coli cells
본 제품은 LMO 제품으로, 고객 분께서 LMO 신고 시스템을 통해 직접 수입 신고를 진행해주셔야 합니다. 자세히보기
TOPO&trade; TA Cloning&trade; Kit, Dual Promoter, with One Shot&trade; TOP10 chemically competent <i>E. coli</i> cells
Invitrogen™

TOPO™ TA Cloning™ Kit, Dual Promoter, with One Shot™ TOP10 chemically competent E. coli cells

빠르고 효율적인 클로닝과 차후 in vitro transcription⁄translation을 위해서는 Invitrogen's TOPO™ TA cloning Dual Promoter Kit와 본사의 인기 제품인 pCR™II vector를자세히 알아보기
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카탈로그 번호수량
K46004050 Reactions
K4600J1010 Reactions
K46000125 Reactions
카탈로그 번호 K460040
제품 가격(KRW)
1,605,000
Online offer
Ends: 31-Mar-2026
1,888,000
할인액 283,000 (15%)
Each
카트에 추가하기
수량:
50 Reactions
제품 가격(KRW)
1,605,000
Online offer
Ends: 31-Mar-2026
1,888,000
할인액 283,000 (15%)
Each
카트에 추가하기
빠르고 효율적인 클로닝과 차후 in vitro transcription⁄translation을 위해서는 Invitrogen's TOPO™ TA cloning Dual Promoter Kit와 본사의 인기 제품인 pCR™II vector를 함께 사용하는 것이 탁월한 선택입니다. 시간이 많이 걸리고 지루한 restriction site cloning 과정을 없앤 TOPO™ cloning은 믿을 수 있는 최고의 방법으로 3단계 프로토콜을 사용해 단 5분 만에 최고 95% recombinant를 수득할 수 있습니다.

TOPO™ TA Dual Promoter Kit와 본사의 pCR™II-TOPO™ TA vector 병용은 다음과 같은 편리한 특징을 갖습니다.

• 3′-T overhangs - Taq-amplified PCR 산물의 direct ligation
• T7 및 SP6 promoters - 효율적인 in vitro transcription
• M13 forward/reverse primer site - sequencing
• EcoR I franking insert를 포함한 편리하고 검증된 restriction site 16개 - 차후 절단 또는 sub-cloning
• 선택한 E. coli에 대한 Kanamycin 및 ampicillin resistance
• 용이한 blue⁄white colony screening - recombinant 선택
• OneShot™ TOP10 Competent cells이 포함 - 편의성과 최고의 cloning 효율을 보장함
For Research Use Only. Not for use in diagnostic procedures.
사양
박테리아 또는 효모 균주TOP10
세포 유형Chemically Competent
클로닝 방법TOPO™-TA
제품라인One Shot
제품 유형Cloning Kit
프로모터T7, SP6
수량50 Reactions
벡터TOPO-TA Cloning Vectors
형식Kit
Unit SizeEach
구성 및 보관
Box 1:
• Topoisomerase I-activated pCR™II-TOPO™ vector
• PCR buffer
• Salt solution
• dNTPs
• Control template
• M13 forward and reverse primers
• Control PCR primers
• Sterile water

Store at -5 to -30°C.
All reagents are stable for 6 months when properly stored.

Box 2:
• One Shot™ Chemically Competent or Electrocomp™ E. coli
• S.O.C. medium
• Supercoiled pUC19 control plasmid.

Store at -68 to -85°C.

자주 묻는 질문(FAQ)

Can I store my competent E. coli in liquid nitrogen?

We do not recommend storing competent E. coli strains in liquid nitrogen as the extreme temperature can be harmful to the cells. Also, the plastic storage vials are not intended to withstand the extreme temperature and may crack or break.

How should I store my competent E. coli?

We recommend storing our competent E. coli strains at -80°C. Storage at warmer temperatures, even for a brief period of time, will significantly decrease transformation efficiency.

What is the difference between the pCR2.1-TOPO and pCR4-TOPO vectors?

The vector backbones for both of these vectors are very similar. The main difference is that the pCR4-TOPO vector has sequencing primer sites located as close as 33 base pairs from the PCR product insertion site. This minimizes the amount of vector DNA sequence that needs to be read before reaching the sequence of the insert, making the pCR4-TOPO vector very useful for sequencing applications.

What is the difference between the pCR2.1-TOPO and pCRII-TOPO vectors?

The vector backbones for both of these vectors are very similar. The main difference is that the pCRII-TOPO vector is a dual promoter vector, containing the SP6 and T7 promoters for in vitro transcription/sequencing, whereas the pCR2.1-TOPO vector contains only the T7 promoter for in vitro transcription/sequencing. Both vectors contain the M13 Forward and Reverse primer sites for sequencing or PCR screening.

Your TOPO cloning kits contain a control template and control primers. Can I obtain the sequence of the control template?

The sequence of the control template is proprietary.

인용 및 참조 문헌 (8)

인용 및 참조 문헌
Abstract
Cloning and functional expression of a thyrotropin receptor cDNA from rat fat cells.
Authors:Endo T; Ohta K; Haraguchi K; Onaya T;
Journal:J Biol Chem
PubMed ID:7738021
Thyrotropin receptor (TSH-R) has been thought to be thyroid-specific, but, by Northern blot analysis, we found that rat adipose tissue expressed TSH-R mRNAs in amounts approaching those in the thyroid. To investigate the function of TSH-R from adipose tissue, we screened a rat fat cell lambda gt11 cDNA library for ... More
Dual DNA binding specificity of ADD1/SREBP1 controlled by a single amino acid in the basic helix-loop-helix domain.
Authors:Kim JB, Spotts GD, Halvorsen YD, Shih HM, Ellenberger T, Towle HC, Spiegelman BM
Journal:Mol Cell Biol
PubMed ID:7739539
'Adipocyte determination- and differentiation-dependent factor 1 (ADD1), a member of the basic helix-loop-helix (bHLH) family of transcription factors, has been associated with both adipocyte differentiation and cholesterol homeostasis (in which case it has been termed SREBP1). Using PCR-amplified binding analysis, we demonstrate that ADD1/SREBP1 has dual DNA sequence specificity, binding ... More
Sequential mutations in the interleukin-3 (IL3)/granulocyte-macrophage colony-stimulating factor/IL5 receptor beta-subunit genes are necessary for the complete conversion to growth autonomy mediated by a truncated beta C subunit.
Authors:Hannemann J, Hara T, Kawai M, Miyajima A, Ostertag W, Stocking C
Journal:Mol Cell Biol
PubMed ID:7739524
'An amino-terminally truncated beta C receptor (beta C-R) subunit of the interleukin-3 (IL3)/granulocyte-macrophage colony-stimulating factor/IL5 receptor complex mediates factor-independent and tumorigenic growth in two spontaneous mutants of a promyelocytic cell line. The constitutive activation of the JAK2 protein kinase in these mutants confirms that signaling occurs through the truncated receptor ... More
A powerful transgenic tool for fate mapping and functional analysis of newly generated neurons.
Authors:Zhang J, Giesert F, Kloos K, Vogt Weisenhorn DM, Aigner L, Wurst W, Couillard-Despres S
Journal:BMC Neurosci
PubMed ID:21194452
Lack of appropriate tools and techniques to study fate and functional integration of newly generated neurons has so far hindered understanding of neurogenesis' relevance under physiological and pathological conditions. Current analyses are either dependent on mitotic labeling, for example BrdU-incorporation or retroviral infection, or on the detection of transient immature ... More
Classical and non-classical Major Histocompatibility Complex class I gene expression in in vitro derived bovine embryos.
Authors:Doyle J, Ellis SA, O'Gorman GM, Aparicio Donoso IM, Lonergan P, Fair T
Journal:J Reprod Immunol
PubMed ID:19682752
The role of the Major Histocompatibility Complex class I (MHC-I) genes in human and mouse preimplantation embryo development has received considerable attention. In contrast, information concerning the role of these genes in bovine embryo development is limited. The objective of the current study was to characterize the expression pattern of ... More