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Agarose - Low Melt, Separation ≤ 1000 bp
Genetic Performance Certified  

MB Grade

Part # Description Unit Size Your Price(USD)
Qty
32829 25 GM
Agarose - Low Melt,
Separation ≤ 1000 bp
Genetic Performance Certified
25gm    $129.00
32829 100 GM
Agarose - Low Melt,
Separation ≤ 1000 bp
Genetic Performance Certified
100gm    $394.00
     

PRODUCT SPECIFICATIONS
Form: Granular, free-flowing powder
EEO (-mr): ≤ 0.10
Gel Point (4%): ≤ 35°C
Remelt Point (4%): ≤ 65°C
Gel Strength (4%): ≥ 1000 gm/cm2
Moisture: ≤ 5%
Residue on Ignition: ≤ 0.3%
Sulfate (SO4): ≤ 0.12%
Genetic Performance Tests:
    DNase: Passes test
    RNase: Passes test
    In-Gel Restriction Enzyme Digestion: Passes test
    In-Gel Ligation: Passes test
    DNA Binding: Passes test
    Gel Background: Passes test
    DNA Resolution: Passes test
    Agarase Digestion: Passes test
Separation Guidelines:
Range of separation in 1X TAE:
    2.0%: 1500 - 100 bp
    3.0%: 700 - 150 bp
    4.0%: 300 - 70 bp
    5.0%: 50 - 10 bp
Range of separation in 1X TBE:
    2.0%: 1000 - 400 bp
    3.0%: 500 - 100 bp
    4.0%: 150 - 10 bp
    5.0%: < 30 bp

Applications:

  1. Enzymatic modification of nucleic acids in re-melted gels.
  2. Separation of DNA or RNA fragments ≤ 1000 bp.
  3. In-gel recovery of nucleic acid fragments.
  4. PCR analysis.
  5. Labile sample procedures.

Isolating DNA from low-melting temperature agarose:
Follow procedure for preparing an agarose gel and be sure to run the electrophoresis at 4°C to keep the gel from melting. Excise the DNA band of interest and transfer it to a microcentrifuge tube. Cut as close to the DNA band as possible to avoid any unnecessary agarose. Add 5 volumes of 20mM Tris-HCl (pH 8.0), 1mM EDTA (pH 8.0) to the tube with the agarose. Cap the tube and heat for 5 minutes at 65°C. The agarose should melt. Cool the solution to room temperature and add an equal volume of equilibrated phenol. Vortex for 20 seconds and spin at 400 x g for 10 minutes (20°C). Remove the aqueous phase (top) to a new microcentrifuge tube. Re-extract with phenol:chloroform and then with chloroform. Precipitate the final aqueous phase with 0.2 volumes of 10mM ammonium acetate and 2 volumes of ethanol. Recover the DNA by centrifugation.

CAS:

9012-36-6

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