Using acrylamide instead
of agarose gives much sharper bands.
If you are analyzing short DNA fragments, run PAGE instead
of agarose to get sharper bands.
Using chondroitin sulfate to improve the viability and biosynthesis of chondrocytes encapsulated in interpenetrating network (IPN) hydrogels
of agarose and poly (ethylene glycol) diacrylate.
The bioactivity
of agarose — PEGDA interpenetrating network hydrogels with covalently immobilized RGD peptides and physically entrapped aggrecan.
He and his colleagues wanted to avoid the classic light - sheet arrangement in which the sample is embedded in a tube
of agarose and surrounded by lasers and cameras.
Not exact matches
The design differs from that
of a conventional commercial microscope: Keller placed the laser and objective lens at right angles to each other atop a table; then he embedded zebrafish embryos in
agarose in a sample tube between the two.
To imitate the cactus root and its outer covering, they made a material composed
of cellulose fibers,
agarose cyrogel and microparticles.
First, they 3 - D - printed wormlike strands
of a gel called
agarose, each serving as a cast
of a tiny blood vessel.
Conditions for the PCR reaction were 40 cycles
of 94 °C for 30 s, 55 °C for 30 s, and 72 °C for 30 s. Amplicons were purified on a 2 %
agarose gel, cloned into plasmid vectors using TOPO TA (Invitrogen, Carlsbad, CA), and sent to an outside company (Elim Biopharmaceuticals, Hayward, CA) for Sanger sequencing in both directions using vector primers M13F and M13R.
When an electric current is applied along the length
of the gel, the DNA starts to migrate through the
agarose thicket.
A 3 - ml overlay consisting
of EMEM with 0.4 %
agarose was added, and the cells were incubated at 37 °C for 72 hours.
Preparation and characterization
of superporous
agarose — reticulated vitreous carbon electrodes as platforms for electrochemical bioassays.
(This is an updated version
of the current DNA Fingerprinting field trip, replacing
agarose gels with the DNA chip.)
The improved size resolution
of the DNA chip allows students to identify their genotype, something impossible with
agarose gel electrophoresis.
Cell extracts (1.5 mg) were incubated with 15 μL
of anti-FLAG M2 -
agarose affinity gel (Sigma - Aldrich, St. Louis, MO).
Ten - microliter aliquots
of the nested PCR products were subjected to RFLP analysis by digestion with 2 U
of either HinfI or MseI, and digested fragments were resolved by
agarose gel electrophoresis in TBE buffer, as described elsewhere [19, 28].
The amplified DNA products were analyzed on a 1.0 %
agarose gel, and pieces
of gel containing the amplified DNA bands were excised and purified using a gel extraction kit (Takara Bio).
Genomic DNA
of clones B31 - A3, ospC7, and ospC7 / ospC +4 was separated through
agarose gels, transferred to a membrane, and hybridized with a 32P - labeled probe specific for ospC.
c, Southern blot (left) membrane hybridization
of 10 µg
of BamHI - digested genomic DNA (see corresponding
agarose gel on right) using a DNA probe from the pCEP backbone.
To generate a full - length unc - 9:: gfp construct, the 14.7 - kb UNC - 9A + B PCR product (representing the 5» end
of unc - 9) and the unc - 9:: gfp plasmid were digested separately with Kpn I, digests electrophoresed through low - melt
agarose (SeaPlaque GTG
agarose, FMC, Rockland, ME, USA), and appropriate fragments purified by phenol extraction and ethanol precipitation.
This product was similarly purified in a low - melt
agarose gel and used at 1 ng / μl along with 50 ng / μl
of the unc - 36 (+) cosmid derivative RIp16 (gift
of L Lobel) for microinjection into unc - 36 -LRB--) animals.
The supernatant was mixed with 300 µl
of Ni - NTA
agarose (Qiagen), and the proteins were allowed to bind for 3 hours, followed by washing with 20 ml
of resuspension buffer, and eluted with 500 µl
of elution buffer (20 mM NaHPO4, 300 mM NaCl, 10 % glycerol, 150 mM Imidazole, pH 7.8).