Electrophoresis Machine With Cell by Scantrik

The most basic electrophoresis system consists of a chamber or cell, a membrane, an incubator or oven, and a power supply. The chamber contains two buffer compartments, one at each end of the chamber. A bridge between the two compartments supports a membrane, typically cellulose acetate or some type of gel.

We are your One Stop Hub Dealer, Supplier, Wholesale, Distributor for Medical Equipment | Hospital Supplies | Lab Consumables | Surgical Instruments | Dental Care | Clinical Devices | PPE Kits | Disinfectants | Consumables & Disposables |Lab Diagnostics & Instruments | Medical Device & Equipment |Medical Implants | Hospital Establishment | Physiotherapy & Rehabilitation-Medical Aids | Mobility Aid | Medical Furniture | Gynaecology & Infant Care | Hospital Holloware | Lab Reagents | Radiology Equipment (Ultrasound, X-ray Machine, CT, MRI, ECG)

WE CAN SUPPLY AND INSTALL ANYWHERE IN NIGERIA
OFFICES IN LAGOS, ABUJA, PORT HARCOURT AND BENIN CITY
Please CALL: 0907-643-3020, 0904-936-7703
WhatsApp: https://wa.me/2349076433020

WhatsApp: https://api.whatsapp.com/send?phone=2349049367703

Email: scantrikmedicalsupplies@gmail.com

Web: www.scantrikmedicalsupplies.ng/products

Instagram: www.instragram.com/scantrikmedicalsupplies

Overview

Features:

  • Power supply
  • Provides an electric current to the chamber to separate charged particles. A good power supply offers precise AC to DC conversion, multiple operating modes, and abnormality alerts. 
  • Chamber
  • Contains two buffer compartments, one at each end, and a membrane that supports the buffer. The chamber also has two electrodes, a cathode and an anode. 
  • Sample loading
  • Samples are loaded into wells in the gel using a pipette. 
  • Separation
  • Charged particles in the sample move through the gel towards the oppositely charged electrode. Smaller molecules move faster than larger molecules. 
  • Visualization
  • The gel is stained to visualize the bands, or the DNA is transferred to a membrane. 
  • Size determination
  • The size of the substance of interest is determined by comparing it to nucleic acid markers of known size.