Agarose High EEO

REQUEST MORE INFO
Catalogue No: abx299903
Price: US$282.75
(Size: 100 g)

Click on the image to see the image legend

Available Options

* Size:





Add to Shopping Cart Buy It Now GET A QUOTE

Documents

Datasheet SDS

High EEO agarose is an agarose designed for the analysis of molecules that exhibit high migration to the cathode. Suitable for the analysis of different nucleic acid fragmnents, in separation techniques such as electrophoresis counterimmunoelectrophoresis, chromotography, blotting and others used in the field of biochemestry and molecular biology.

Specification:

Moisture≤ 10%
Gel strength (1.5% gel)≥ 1200 g/cm2
Gelling point (1.5% gel)41-45 °C
Melting point (1.5% gel)84-88 °C


Target Agarose High EEO
Storage Store at room temperature.
Availability Shipped within 10-15 working days.
Note This product is for research use only.
Directions for use Preparation of agarose gel in a microwave:
  1. Determine the amount of gel and reagents required to prepare the gel at the desired concentration.
  2. Add an appropriate volume of run buffer (TAE, TBE to 1X).
  3. Homogenize and microwave for 2 - 4 minutes, in cycles of 30 seconds, until the sample is completely dissolved. It is recommended to run the microwave at medium power. Caution: Use necessary protection for the handling of hot material.
  4. Add staining reagent (e.g. Ethidium Bromide) and homogenize.
  5. Allow to cool to 60° C before casting. After casting, allow to cool and gel to room temperature
  6. Mount the electrophoresis chamber, load samples and run buffer (same buffer with which the gel was prepared) and start the electrophoretic run.

Preparation agarose gel on a hot plate.
  1. Determine the amount of gel and reagents required to prepare the gel at the desired concentration.
  2. Add an appropriate volume of run buffer (TAE, TBE to 1X).
  3. Homogenize and heat on a hot plate with stirring. Once boiling has started, start a timer for 20 minutes (use a lid or refrigerant system to avoid concentrating the sample).
  4. Add staining reagent (e.g. Ethidium Bromide) and homogenize.
  5. Allow to cool to 60° C before casting. After casting, allow to cool and gel to room temperature
  6. Mount the electrophoresis chamber, load samples and run buffer (same buffer with which the gel was prepared) and start the electrophoretic run.
Research Articles on Agarose High EEO


Write a review

Tags:
(Click to show)