Sanshibio taq DNA polimerasi (Mg2+ Plus) 10 X 5000U

Taq DNA polimerasi

oggetto numero：E001A Specificazione：500U/1000U/5000U Storage: Conservare a -20 ° C.

Introduzione al prodotto：

This product is Taq DNA Polymerase, commonly referred to as Taq enzyme, which is one of the most widely used DNA polymerases. It is expressed in Escherichia coli with the cloned gene of Thermus aquaticus DNA Polymerase and then purified through multiple steps. IL PCR products amplified using this product have an added A base at the 3′ end, allowing for cloning into T vectors.

Contenuto del prodotto：

Componenti	E001A-01（500U）	E001A-02（1000U）	E001A-03（5000U）
Taq DNA Polymerase（5U/µL）	100µl	200µl	1ml
dNTP Mixture (10mm ciascuno)	100µl	200µl	1ml
10× PCR Buffer (Mg2+ più)	1ml	2× 1mL	10× 1mL

Magazzinaggio:

Conservare a -20 ° C., con una durata minima di conservazione di 12 mesi.

Definizione dell'attività:

Using activated largemouth bass sperm DNA as a template/primer, the intake of 10 nmol of total nucleotides as acid-insoluble material within 30 minutes at 74°C is defined as 1 unit of activity (U).

Controllo di qualità:

This product has undergone quality testing and is free from endonuclease activity, exonuclease activity, e contaminazione da ribonucleasi. Residual host genomic DNA is below 10 copie.

Product Usage:

Amplification of DNA using PCR method; DNA sequence determination.

Istruzioni di utilizzo:

• Dissolve and mix all required solutions for the PCR reaction and place them on an ice bath or in a cooler. It is recommended to aliquot the PCR reaction mixture to avoid repeated freeze-thaw cycles.
• It is advisable to set up the PCR reaction system on an ice bath or in a cooler, following the recommended reaction system for reference.
• Excessive template DNA can lead to nonspecific PCR products. Recommended template amounts for different types of templates in a 50µL reaction volume are as follows:

Genomic DNA from Animals and Plants: 0.1-1mg;

Genomic DNA from Escherichia coli: 10-100Di;

DNA plasmidico: 0.1-10Di.

Recommended Reaction System:

Reagenti	50µL System Volume	Concentrazione finale
Taq DNA polimerasi	1µl	0.1U
10× PCR Buffer (Mg2+ più)	5µl	1×
dNTP Mixture (10mm ciascuno)	1µl	0.2mm ciascuno
Primer i (10µm)	1µl	0.2µm
Primer II (10µm)	1µl	0.2µm
DNA modello	1µl	-
Ddh2O	To 50µL	-

Nota: Le quantità di ciascun componente nel sistema di reazione possono essere regolate in base ai requisiti effettivi.

• Thoroughly pipette and mix the prepared reaction system using a pipette, seal the PCR tubes with caps, label them appropriately, and briefly centrifuge at room temperature.
• Place the prepared PCR tubes into the Macchina per PCR, set the reaction conditions, and initiate the PCR reaction.

Reaction Conditions:

Metodo/passaggi	Time setting	Cicli
95℃ (Pre-denaturazione)	2-5min	1
95℃ (Denaturazione)	30sec	25-35 Cicli
55℃-60℃ (Ricottura)	30sec
72℃ (Estensione)	1min
72℃ (Final Extension)	10min	1
4℃ (Hold)	∞	-

Nota: Le condizioni di reazione possono essere regolate e ottimizzate in base ai requisiti effettivi.

Precauzioni:

1. Extension time can be adjusted based on factors such as the length and GC content of the PCR product. The extension time per kb of the product is closely related to the complexity of the template: simple templates require 20 secondi, typical templates require 30 secondi, and complex templates require 1 minuto.
2. The setup of the PCR reaction should be tailored to different conditions such as template, primer, length of PCR product, and GC content. The final concentration of primers typically falls within the range of 0.1-1.0μM. DNA template concentration can be adjusted accordingly. For complex templates or high GC content, it’s recommended to prolong pre-denaturation/denaturation or extension times and increase denaturation/annealing temperatures.
3. Use designated areas and pipettes before and after amplification, indossare guanti, e cambiarli frequentemente. Dopo aver completato la reazione PCR, do not open the reaction tubes immediately. Allow them to cool sufficiently at 4°C or -20°C before opening to minimize the risk of PCR product contamination to the laboratory environment.