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PCR Lab Equipment Thermal Cycler Thermocycleur

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Payment Type:

L/C,T/T

Incoterm:

EXW,FOB

Min. Order:

1 Set/Sets

Transportation:

Ocean,Land,Air,Express

Port:

Shanghai

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Product Description

Product Attributes
Supply Ability & Additional Information
Packaging & Delivery

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Overview

Product Attributes

Model No.: General 2215

Brand: General

Types Of: Genes &Amp; Life Science Equipments

Place Of Origin: China

Warranty Service: 1 Year

After-sales Service: Online Technical Support, Return And Replacement, Free Spare Parts

Warranty: 1 Year

Place Of Origin: China

After-sale Service: Online Technical Support

Instrument Classification: Class Iii

Light Source: Halogen

Brand Name: Superyears

Model Number: General 2215

Applicable Consumables: 0.1ml 96-well plate, 8-strip tube, single tube

Channel: 5

Maximum Temperature Rise And Fall Speed: 5.5°C /S

Running Time: 40 min

Sensitivity: 1 copy of human Gene

Dynamic Range: 9 Logs

Reliability: between 5000 copies and 10000 copies is 99.7%

N.W.: 35KGS

Type: Genes & Life Science Equipments

Photo Design: Upper photo design

Supply Ability & Additional Information

Packaging: Carton

Productivity: 30packs/month

Transportation: Ocean,Land,Air,Express

Place of Origin: CHINA

Supply Ability: 100 Set/Sets per Month

Port: Shanghai

Payment Type: L/C,T/T

Incoterm: EXW,FOB

Packaging & Delivery

Selling Units:: Set/Sets

Package Type:: Carton

Picture Example:

PCR Lab Equipment Thermal Cycler Thermocycleur

RT-qPCR Instrument Description

We use sample DNA put into the thermocycler to separate the DNA strands. Then, the targeted DNA strand will be hybridized by adding up the Left and Right probe oligonucleotides. The ligase enzyme will bind the probe oligos up immediately to adjacent target on the sample DNA. Therefore, the hybridized Left and Right probe oligo start catalyzing the creation of a covalent bond in between. Once the probe oligos are sealed, MLPA probes will be exponentially amplified using the single PCR primer pair.

Real-Time PCR reaction consists of the three steps: denaturation, primer annealing and primer elongation. Those steps of PCR amplification are repeated many times. The fluorescence labelled primer is incorporated into the size of the amplification products that will go through the capillary electrophoresis to pass a detector. The measured fluorescence is visualized as a peak pattern, the so-called electropherogram. The raw data from the capillary electrophoresis analyzer forms the input of the MLPA analysis.

Real Time Fluorescence Quantitative Pcr System Display