TOPO™ TA Cloning™ Kit for Subcloning, with One Shot™ TOP10 chemically competent E. coli cells
TOPO&trade; TA Cloning&trade; Kit for Subcloning, with One Shot&trade; TOP10 chemically competent <i>E. coli</i> cells
Invitrogen™

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

TOPO™ TA Cloning™ Kits for Subcloning provide a highly efficient, 5-minute, one-step cloning strategy ('TOPO™ cloning') for the direct insertion深入閱讀
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產品號碼Quantity
K45004050 Reactions
K4500J1010 Reactions
K45000125 Reactions
產品號碼 K450040
價格 (TWD)
33,450.00
線上優惠
Ends: 31-Dec-2025
44,600.00
您節省 11,150.00 (25%)
Each
新增至購物車
Quantity:
50 Reactions
價格 (TWD)
33,450.00
線上優惠
Ends: 31-Dec-2025
44,600.00
您節省 11,150.00 (25%)
Each
新增至購物車
TOPO™ TA Cloning™ Kits for Subcloning provide a highly efficient, 5-minute, one-step cloning strategy ('TOPO™ cloning') for the direct insertion of Taq polymerase–amplified PCR products into a plasmid vector for subcloning. Each kit uses the pCR™ 2.1-TOPO™ TA vector with convenient restriction sites for subcloning. The cloning kits are available with a variety of competent cells, or without competent cells, depending upon your needs and budget. Features of the TOPO™ TA Cloning™ Kits for Subcloning:

Fast and easy—go from PCR to clones in just 3 steps and in as little as 5 minutes hands-on time
Efficient—obtain up to 95% clones with correct insert
Proven—reliable performance for over a decade with over 4,000 citations
Simple—no ligase, post-PCR procedures, or PCR primers containing specific sequences are required

TOPO™ TA Cloning™ Kits for Subcloning—overview

Vector: pCR™ 2.1-TOPO™ TA vector—subcloning vector with 15 convenient restriction sites flanking your insert for easy, directional subcloning
Cloning method: TOPO™ TA Cloning™ —Topoisomerase I–based, 5-minute ligation of PCR products with 3′-A overhangs (Taq polymerase amplified) to TOPO™ vector with T overhangs
Competent cells: various options—choose from kits with either general, high-efficiency, bacteriophage T1–resistant, fast-growing competent cells, or use your own

pCR™ 2.1-TOPO™ TA vector—cloning and subcloning simplicity
The pCR™ 2.1-TOPO™ TA vector is linearized with 3'-thymidine (T) overhangs for direct ligation of Taq polymerase–amplified PCR products (TA cloning™) and is 'activated' with covalently bound Topoisomerase I. There is no need to add ligase and cloning is complete in 5 minutes. EcoRI sites flanking the PCR product insertion site allow for easy excision of inserts or use any combination of 15 convenient restriction sites flanking your PCR insert for easy, directional subcloning.

pCR™ 2.1-TOPO™ TA clone selection and manipulation
The pCR™ 2.1-TOPO™ TA vector contains both ampicillin and kanamycin resistance markers and the LacZα gene for blue/white screening.

Simplified TOPO™ -based cloning
Using TOPO™ cloning technology, there is no need for PCR primers containing specific sequences, post-PCR procedures, vector preparation, or other time-intensive DNA manipulation steps. Just add your PCR reaction straight to the provided topoisomerase-charged vector, incubate 5 minutes, and transform E. coli competent cells.

Efficient cloning
With up to 95% of clones carrying the desired insert, you can screen less clones, saving time and money. The pCR™ 2.1-TOPO™ TA vector used in this kit comes with 3'-T overhangs for efficient ligation of Taq polymerase–amplified PCR products, which contain 3'-A overhangs.

The standard in cloning
When it comes to cloning, TOPO™ cloning technology has been a reliable partner for thousands of scientists for over ten years. Fast, simple-to-use, and efficient, TOPO™ cloning has been applied to many different vectors for a wide array of applications.

TOPO™ TA Cloning™ Kits for Subcloning—kit options
The TOPO™ TA Cloning™ Kit for Sequencing can be purchased with a variety of competent cells that deliver different advantages depending upon your needs:

• General cloning: TOP10 cells (Cat. No. K4500-01, K4500-40)
• High-efficiency cloning: TOP10 Electrocomp™ Cells (Cat. No. K4560-01, K4560-40)
• General cloning, bacteriophage T1 resistance: DH5α-T1R cells (Cat. No. K4520-01, K4520-40)
• Fast growth: Mach1™ -T1R Chemically Competent E. Coli (Cat. No. K4510-20)
• Provide your own: for flexibility and to save money (Cat. No. 450641)

We also offer two versions of the kit that include a PureLink™ Quick Plasmid Miniprep Kit (Cat. No. K4500-02 and K4510-02) for use in isolation of clean, sequencing-ready, recombinant plasmid.
For Research Use Only. Not for use in diagnostic procedures.
規格
Bacterial or Yeast StrainTOP10
Cell TypeChemically Competent
Cloning MethodTOPO™-TA
Product LineOne Shot
Product TypeCloning Kit
Quantity50 Reactions
VectorTOPO-TA Cloning Vectors
FormatKit
Unit SizeEach
內容物與存放
Box 1:
• Topoisomerase I-activated pCR™2.1-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.

常見問答集 (常見問題)

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.

引用資料與參考文獻 (12)

引用資料與參考文獻
Abstract
Autoregulation of pituitary corticotroph SOCS-3 expression: characterization of the murine SOCS-3 promoter.
Authors:Auernhammer CJ, Bousquet C, Melmed S
Journal:Proc Natl Acad Sci U S A
PubMed ID:10359822
'Pituitary corticotroph SOCS-3 is a novel intracellular regulator of leukemia inhibitory factor (LIF)-mediated proopiomelanocortin gene expression and adrenocorticotropic hormone (ACTH) secretion, inhibiting LIF-activated Janus kinase-signal transducers and activators of transcription (STAT) signaling in a negative autoregulatory loop. We now demonstrate in corticotroph AtT-20 cells that LIF-stimulated endogenous SOCS-3 mRNA expression ... More
Single base mismatches in the mRNA target site allow specific seed region-mediated off-target binding of siRNA targeting human coagulation factor 7.
Authors:Ravon M, Berrera M, Ebeling M, Certa U
Journal:RNA Biol
PubMed ID:22258146
'We have analyzed the off-target activity of two siRNAs (F7-1, F7-2) that knock-down human blood coagulation factor 7 mRNA. F7-1 modulates a significant number of non-target transcripts while F7-2 shows high selectivity for the target transcript under various experimental conditions. The 3''-UTRs of all F7-1 off-target genes show statistically significant ... More
A host-specific function is required for ligation of a wide variety of ribozyme-processed RNAs.
Authors:Reid CE, Lazinski DW
Journal:Proc Natl Acad Sci U S A
PubMed ID:10618434
'Hepatitis delta virus (HDV) replicates its circular RNA genome via a rolling circle mechanism. During this process, cis-acting ribozymes cleave adjacent upstream sequences and thereby resolve replication intermediates to unit-length RNA. The subsequent ligation of these 5''OH and 2'',3''-cyclic phosphate termini to form circular RNA is an essential step in ... More
Characterization of a Ustilago maydis gene specifically induced during the biotrophic phase: evidence for negative as well as positive regulation.
Authors:Basse CW, Stumpferl S, Kahmann R.
Journal:Mol Cell Biol
PubMed ID:10594035
The phytopathogenic basidiomycete Ustilago maydis requires its host plant, maize, for completion of its sexual cycle. To investigate the molecular events during infection, we used differential display to identify plant-induced U. maydis genes. We describe the U. maydis gene mig1 (for  ... More
Genetic engineering of phytochrome biosynthesis in bacteria.
Authors: Gambetta G A; Lagarias J C;
Journal:Proc Natl Acad Sci U S A
PubMed ID:11553807
The bilin prosthetic groups of the phytochrome photoreceptors and the light-harvesting phycobiliprotein antennae arise from the oxygen-dependent ring opening of heme. Two ferredoxin-dependent enzymes contribute to this conversion: a heme oxygenase and a bilin reductase with discrete double-bond specificity. Using a dual plasmid system, one expressing a truncated cyanobacterial apophytochrome ... More