GelRed® Nucleic Acid Gel Stain | Biotium
GelRed® can also be used to stain polyacrylamide gels via post gel staining. GelRed® is also compatible with downstream DNA manipulations such as restriction digest, sequencing, and cloning. GelRed® and EtBr have virtually the same spectra, so
i-gel®, supraglottic airway, size 1.0, neonate, 2-5kg. 8705000. i-gel®O2 Resus Pack, large adult – includes a size 5 i-gel O2 with orange hook ring, sachet of lubricant, airway support strap and a 12FG suction tube, 90+kg. 8704000. i-gel®O2 Resu
O’RangeRuler 20 bp DNA Ladder, ready-to-use
O'RangeRuler 20 bp DNA Ladder is supplied with 6X Orange DNA Loading Dye for sample DNA. Orange G dye can be used to monitor DNA migration in agarose or polyacrylamide gels and migrates at 50 bp in a 1% agarose gel. It is the preferable dye
For all except Orange G use 25 mg of dye, add either 10 ml of 60% glycerol solution or 4 g of sugar and make up to 10 ml with distilled water. For Orange G use 100 mg of dye and make up as above. The Orange G is only 50 bp in size and is easily
TGX FastCast Acrylamide Solutions | Life Science Research | Bio-Rad
TGX FastCast premixed acrylamide solutions bring all the benefits of TGX gel chemistry to handcast polyacrylamide gels. TGX (Tris-Glycine eXtended) chemistry retains Laemmli-like separation characteristics while using a standard Tris-glycine
Thermo Scientific GeneRuler Low Range DNA Ladder is recommended for sizing and approximate quantification of a double-stranded DNA in the range of 25 bp to 700 bp on agarose or polyacrylamide gels. The DNA ladder consists of 10 DNA fragments and
Fabrication and photocatalytic performance of Bi24O31Br10 nanosphere by a polyacrylamide gel method - He - 2025 - Micro & Nano Letters - Wiley
BET, m 2 /g Reference polyacrylamide gel method 70.12 in this Letter solvothermal method with the help of soluble starch 12.8 [] ion-exchange approach to the fabrication 67.16 [] solvothermal method 36.0 [ 16.3
degraded Repeat the PCR with different primer concentrations from 0.1–0.5 µM of each primer (in 0.1 µM steps). In particular, when performing highly sensitive PCR, check for possible degradation of the primers on a denaturing polyacrylamide
A method for synthesizing copper nanoclusters based on protein–polyacrylamide gel and its application
Copper nanoclusters (NCs) are increasingly favored by many researchers in the field of biochemistry. In this study, we have provided a method for the preparation of copper NCs based on a protein “turn-on” method, i.e. by immobilizing low-emissiv
Agarose and Metaphor Gels. 1.Add agarose to 1X TBE (or TAE) buffer. For gel size 20 x 24 cm, use 300-400 ml buffer and 0.7 to 1.0% agarose. 2. Melt agarose in 500 ml flask in microwave oven, mixing several times during heating. Let cool to 55 C
Blue/Orange Loading Dye, 6X - Promega Corporation
3ml. Your price: Blue/Orange Loading Dye, 6X, is a convenient marker dye containing 0.4% orange G, 0.03% bromophenol blue, 0.03% xylene cyanol FF, 15% Ficoll® 400, 10mM Tris-HCl (pH 7.5) and 50mM EDTA (pH 8.0). It is provided in a premixed,
Product Details. The MinElute Gel Extraction Kit provides spin columns, buffers, and collection tubes for silica-membrane-based purification of DNA fragments of 70 bp – 4 kb from up to 400 mg gel slices. The spin columns are designed to allow
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