WebSep 27, 2013 · The modified DNA polymerase comprises modifications of at least two amino acids selected from the group consisting of amino acids corresponding to Y7, P36, and V93 in SEQ ID NO: 1, in the amino acid sequence represented by any one of SEQ ID NOs: 1 to 10. Latest TOYOBO CO., LTD. Patents: MONOACYLATED MEL-PRODUCING … WebToyobo has 333 material(s) in the MatWeb database. Back to Manufacturer List. Toyobo A1061D Thermoplastic Polyurethane Elastomer, Injection Grade. Toyobo A1064D …
TOYOBO
WebGreater yield—extension speed is 2X faster than Taq DNA polymerase and 5X faster than Pfu DNA polymerase Higher processivity—sequential nucleotide polymerization is 10- to 15-fold greater than Pfu and Tli DNA polymerases Amplifies plasmid and lambda DNA templates up to 6 kbp Amplifies genomic DNA templates up to 2 kbp WebThis kit includes the following components for 250 reactions, 20 μL total reaction volume. All reagents should be stored at -20°C. < HSTTX-101 >. 2x Buffer for rTth/ TTx (DNA) 1.25 mL x 2. Hot Start TTx DNA Polymerase (4U/ μL) 62.5 μL. Note: 2x Reaction Buffer contains essential components for the reaction (buffer, salts, Mg2+, dATP, dCTP ... gavin broussard ldnr
GLAMIDE T-423 - Toyobo - SpecialChem
WebJun 14, 2012 · The DNA concentration and purity were assessed using a spectrophotometer (NanoDrop 2000c; Thermo Scientific, Wilmington, DE, USA). The PCR test used Blend Taq Plus (Toyobo Co. Ltd. Osaka, Japan) and followed its manufacturer’s protocol except for down-scaling to 20 μl in total. WebOct 15, 2024 · To identify the bacterial species, the genome was extracted from bacterial colonies and the 16S rRNA gene was amplified from total DNA by PCR with Blend Taq-Plus DNA polymerase (Toyobo) using the previously described primers 27f (5′-AGAGTTTGATCMTGGCTCAG-3′) and 1525r (5′-AGGAGGTGWTCCARCC-3′) (Ochiai et al., … WebArticle Snippet: PCR reactions were performed in reaction volumes of 25 μl containing 10 ng of genomic DNA templates, 1× PCR Buffer ( Toyobo, Osaka, Japan), 0.2 mM of dNTPs, 0.2 μM of each primer and 1.25 U Blend Taq (Toyobo). Techniques: Polymerase Chain Reaction, Marker, Negative Control Journal: Molecular Biotechnology gavin brown baseball