 Click this icon to add products to compare list. Select up to 10 products. |
10 x Taq Buffer is a ready-to-use buffer to be used for Taq, Hot Taq, Red Taq and Long Taq enzymes in PCR reactions. Does not contain MgCl2.
10 x Taq Buffer with (NH4)2SO4 is a ready-to-use buffer to be used for Taq, Hot Taq, Red Taq and Long Taq enzymes in PCR reactions. Does not contain MgCl2.
Consists of multiple repeats of 100-bp fragments from 100 bp up to 1000 bp. Supplied in sufficient quantity for 100 loadings using 4-5 ul per loading. Not designed for quantitating DNA concentration in a sample. Ladders available to be mixed with loading dye of choice.
Consists of multiple repeats of 100-bp fragments from 100 bp up to 1000 bp. Supplied in sufficient quantity for 100 loadings using 4-5 ul per loading. Not designed for quantitating DNA concentration in a sample. Ladders available premixed as ready-to-use format premixed with loading-dye-solution (Express).
HotTaq PCR mix is a prepared solution containing everything needed for successful PCR reaction except specific primers and DNA template. The mix includes highquality recombinant Taq DNA polymerase, nucleotides in a specifically optimized buffer formulation. For reaction set-up add the PCR Mix (25 ul) to the primers, template and water (is provided in the set; total volume of 50 ul). PCR Mix is provided with MgCl2 in the solution.
2 x RedTaq PCR Mix with MgCl2 is a prepared solution containing everything needed for successful PCR reaction except specific primers and DNA template. The mix includes highquality recombinant LongTaq DNA polymerase, nucleotides in a specifically optimized buffer formulation. For reaction set-up add the PCR Mix (25 ul) to the primers, template and water (is provided in the set; total volume of 50 ul). PCR Mix is provided with MgCl2 in the solution.
Taq PCR mix is a prepared solution containing everything needed for successful PCR reaction except specific primers and DNA template. The mix includes highquality recombinant Taq DNA polymerase, nucleotides in a specifically optimized buffer formulation. For reaction set-up add the PCR Mix (25 ul) to the primers, template and water (is provided in the set; total volume of 50 ul). PCR Mix is provided with MgCl2 in the solution.
25 mM MgCl2 can be used for optimization of magnesium ion concentration in PCR reaction.
6 X DNA loading Dye is useful for loading DNA samples into wells on agrarose gel electrophoresis. It contains EDTA, glycerol, bromphenol blue and 10 mM Tris-HCl (pH8.0).
Ideal for everyday analysis of nucleic acids by gele electrophoresis or blotting (Northern or Southern) and is also suitable for protein applications. No background fluorescence has been detected by ethidium bromide assay. DNase/RNase-free.
E.coli harboring the plasmid encoding the gene of alkaline phosphatase from Shewanella sp. SIB1 (PAP).
Blood/Cultured Cell Total RNA Purification Kit is designed specifically for purifying total RNA from fresh whole human blood and cultured animal cells.
Cultured Cell Total RNA Purification Kit was designed specifically for purifying total RNA from cultured animal cells.
DEPC-treated Water is can be used in various applications in molecular biology, paticulary for use of RNA. The DEPC-treated Water was prepared by 0.1 % DEPC-treatment and autoclave of highly purified water. The product was confirmed to be RNase-free and DNase free. Apperance is clear liquid.
DNA Marker High is useful for determination of DNA fragments 300 bp to 10,000 bp in size. The DNA size marker consists of 13 double-stranded, blunt-end DNA fragments. The DNA bands close to each other, 525 bp and 500 bp, are for reference indicators. These DNA fragments were fixed amount in solution of DNA Marker High, which makes it possible to estimate amount of DNA. The DNA Marker High is supplied in a ready-to-use mixture containing 8 mM EDTA, 8 % glycerol, 0.015 % bromphenol blue and 10 mM Tris-HCl (pH8.0)
DNA Marker Low is useful for determination of DNA fragments 50 bp to 1,000 bp in size. The DNA size marker consists of 10 double-stranded, blunt-end DNA fragments. The DNA bands close to each other, 550 bp and 500 bp, 120 bp and 100 bp, are for reference indicators. These DNA fragments were fixed amount in solution of DNA Marker Low, which makes it possible to estimate amount of DNA. The DNA Marker Low is supplied in a ready-to-use mixture containing 8 mM EDTA, 8 % glycerol, 0.015 % bromphenol blue and 10 mM Tris-HCl (pH8.0)
DNA Marker Middle is useful for determination of DNA fragments cloned in a plasmid DNA. The DNA size marker consists of 14 double-stranded, blunt-end DNA fragments. The size of 2, 686 bp fragment is the same size of pUC18/19. The DNA bands close to each other, 2, 686 and 3,000 bp, 550 bp and 500 bp, are for reference indicators. These DNA fragments were fixed amount in solution of DNA Marker Middle, which makes it possible to estimate amount of DNA.The DNA Marker Middle is supplied in a ready-to-use mixture containing 8 mM EDTA, 8 % glycerol, 0.015 % bromphenol blue and 10 mM Tris-HCl (pH8.0).
The dsRNA Marker consists of ten double-stranded RNAs, 10, 20, 30, 50, 100, 200, 300, 400, 500 and 1,000 base pairs. The dsRNA Marker is an ideal size marker for determinating sizes of double-stranded RNAs. A twenty bp of RNA band including in the dsRNA Marker is adjusted to approximately 25 ng/ul in concentration. The dsRNA Marker is manufactured for non-denaturing polyacrylamide gel electrophoresis. The dsRNA Marker can be visualized by UV light after ethidium bromide staining.
The dsRNA Marker Easy is supplied in a ready-to-load mixture of loading dye (containing Tris-HCl buffer, glycerol, EDTA sodium salt, sodium chloride, bromphenol blue) and an ideal size marker for determinating sizes of double-stranded RNAs. The dsRNA Marker Easy consists of ten double-stranded RNAs, 10, 20, 30, 50, 100, 200, 300, 400, 500 and 1,000 base pairs. In 5 ul of the dsRNA Marker Easy, a 20 bp of dsRNA is approximately 50 ng. The dsRNA Marker Easy can be visualized by UV light after ethidium bromide staining.
HotTaq DNA polymerase catalyzes 5'-3' synthesis of DNA. The enzyme has been proved not having the 3'-5' exonuclease activity. Prior the first PCR step the HotTaq DNA polymerase should be activated by 15 minute incubation at 95-97°C.
