titanium taq dna polymerase (TaKaRa)
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TaKaRa
titanium taq dna polymerase
Titanium Taq Dna Polymerase, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 1588 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/titanium+taq+dna+polymerase/Titanium+Taq+DNA+Polymerase/bio_rxiv__64898__2026__09__24__754062-308-13-17
Average 96 stars, based on 1588 article reviews
Titanium Taq Dna Polymerase, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 1588 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/titanium+taq+dna+polymerase/Titanium+Taq+DNA+Polymerase/bio_rxiv__64898__2026__09__24__754062-308-13-17
Average 96 stars, based on 1588 article reviews
titanium taq dna polymerase - by Bioz Stars,
2026-10
96/100 stars
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Polymerase Chain Reaction:Article Title: Mapping the Hypoxic Fitness Landscape of Retinal Pigment Epithelial Cells. Article Snippet: After more than 10 population doublings, 40 million cells per replicate for each condition were pelleted, and genomic DNA was extracted from the frozen pellets using the MacheryNagel NucleoSpin Blood L Midi kit (Macherey-Nagel, Düren, Germany; distributed by Takara Bio, San Jose, CA, USA) according to the manufacturer’s instructions. .. To achieve >500× coverage of the Brunello library (assuming 6 μg of genomic DNA per 1 million cells), 24 separate 100 μL PCR reactions were performed with 10 μg of genomic DNA in each reaction, using Article Title: Effects of Mango–Maize and Mango–Cassava Agroforestry Systems on Arbuscular Mycorrhizal Fungi Communities and Soil Properties in Southern Ethiopia Article Snippet: .. PCR reactions were performed on a BioRad T100 thermal cycler (Bio-Rad Laboratories, CA, USA) in a 20 μl reaction volume containing 0.15 mM of each dNTP, 0.5 μM of each primer, 1× Titanium Taq PCR buffer, 1 U Article Title: Constitutive interferon epsilon expression shapes antiviral epithelial states in the female reproductive tract and intestine. Article Snippet: .. Geno typing of the resulting pups was carried out by extracting genomic DNA from toe biopsies using a lysis buffer containing 50 mM Tris-base (pH 8.0), 50 mM KCl, 2.5 mM EDTA, 0.45% IGEPAL CA-630 (NP40), 0.45% Tween-20, and 20 mg/mL proteinase K, followed by incubation at 94°C for 10 min. PCR amplification was performed with primers flanking the gRNA target sites (forward: TCCCAGAACTGGAGTGGT; reverse: AA GAGCCAACAGGGGATTT) using Lysis:Article Title: Constitutive interferon epsilon expression shapes antiviral epithelial states in the female reproductive tract and intestine. Article Snippet: .. Geno typing of the resulting pups was carried out by extracting genomic DNA from toe biopsies using a lysis buffer containing 50 mM Tris-base (pH 8.0), 50 mM KCl, 2.5 mM EDTA, 0.45% IGEPAL CA-630 (NP40), 0.45% Tween-20, and 20 mg/mL proteinase K, followed by incubation at 94°C for 10 min. PCR amplification was performed with primers flanking the gRNA target sites (forward: TCCCAGAACTGGAGTGGT; reverse: AA GAGCCAACAGGGGATTT) using Incubation:Article Title: Constitutive interferon epsilon expression shapes antiviral epithelial states in the female reproductive tract and intestine. Article Snippet: .. Geno typing of the resulting pups was carried out by extracting genomic DNA from toe biopsies using a lysis buffer containing 50 mM Tris-base (pH 8.0), 50 mM KCl, 2.5 mM EDTA, 0.45% IGEPAL CA-630 (NP40), 0.45% Tween-20, and 20 mg/mL proteinase K, followed by incubation at 94°C for 10 min. PCR amplification was performed with primers flanking the gRNA target sites (forward: TCCCAGAACTGGAGTGGT; reverse: AA GAGCCAACAGGGGATTT) using Amplification:Article Title: Constitutive interferon epsilon expression shapes antiviral epithelial states in the female reproductive tract and intestine. Article Snippet: .. Geno typing of the resulting pups was carried out by extracting genomic DNA from toe biopsies using a lysis buffer containing 50 mM Tris-base (pH 8.0), 50 mM KCl, 2.5 mM EDTA, 0.45% IGEPAL CA-630 (NP40), 0.45% Tween-20, and 20 mg/mL proteinase K, followed by incubation at 94°C for 10 min. PCR amplification was performed with primers flanking the gRNA target sites (forward: TCCCAGAACTGGAGTGGT; reverse: AA GAGCCAACAGGGGATTT) using Article Title: Context-specific genetic interaction mapping reveals combinatorial KRAS/FGFR dependence in pancreatic cancer Article Snippet: .. Amplification and barcoding were carried out using P5/P7 primers (Integrated DNA Technologies) and |