Reviews Dna Extraction Pcr Tubes

Taq DNA Polymerase (5,000 Units:5 U/ul)

  • dGTP, dCTP and dTTP also available with us..
  • Applications PCR amplification of DNA fragments DNA labeling and DNA sequencing PCR for cloning. Quality Control No contaminating endonuclease or exonuclease activity detected. Functionally tested in PCR.
  • Applications PCR amplification of DNA fragments up to 5 kb DNA labeling and DNA sequencing PCR for cloning. Quality Control No contaminating endonuclease or exonuclease activity detected. Functionally tested in PCR.
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Genomic DNA Extraction Kit (Bacteria), 50 Preps, 10644 -from Cepham Life Sciences

  • Isolate genomic DNA from both Gram-positive & Gram-negative bacteria.
  • High yield, high quality DNA for sensitive downstream applications including sequencing, PCR & qPCR.
  • Spin columns-collection tubes- 2 mL (50/bag).
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Edvotek 109 DNA Fingerprinting I - I.D. of DNA by Restriction Fragmentation Patterns, for 8 Gels

  • Use your extra Miniprep reagents with UPrep Spin Columns!.
  • Simply follow the kit manufacturer's purification protocol using UPrep Spin Columns.
  • Purify up to 5µg DNA or RNA in as little as 6µl eluate with complete elution and no binding/wash buffer carryover!.
  • UPrep Micro columns are ideal for PCR purification, Gel extraction, RNA Clean-up and gDNA microprep (up to 5µg).
  • Use standard UPrep Spin Columns (cat# 88-143, 88-243C) for plasmid miniprep, PCR purification, RNA Clean-up and gDNA Miniprep (up to 25µg).
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HotStart 2xTaq DNA Pol Master Mix,1ML, P03-CR03SM-1ML

  • Contains 1 ml of 2xMasterMix, 25 mM MgCl2, nuclease free water and DMSO. 2XMasterMix is premixed with sample loading dye for immediate loading after the PCR reaction..
  • HotStart PCR for specific amplification. Comparable with the Platinum Taq polymerase. Good for TA cloning..
  • Dye Minus HotSatrt 2X Master Mix is also available upon request..
  • Applications PCR amplification of DNA fragments up to 10 kb DNA labeling and DNA sequencing PCR for cloning. Quality Control No contaminating endonuclease or exonuclease activity detected. Functionally tested in PCR.
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dATP, dGTP, dTTP, dCTP 100mM Each, 4 x 0.25 ML

  • Box contains contains 1 ml of 2xMasterMix, 25 mM MgCl2, nuclease free water and DMSO. 2XMasterMix is premixed with sample loading dye for immediate loading after the PCR reaction..
  • Stable at room temperature. Long term storage at -20^oC required..
  • Applications PCR amplification of DNA fragments up to 10 kb DNA labeling and DNA sequencing PCR for cloning. Quality Control No contaminating endonuclease or exonuclease activity detected. Functionally tested in PCR..
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dNTP Mix P03-CR04-10, 10mM, 1ML

  • dATP, dGTP, dCTP and dTTP 100mM stock solutions are also available with us..
  • Applications PCR amplification of DNA fragments DNA labeling and DNA sequencing PCR for cloning. Quality Control No contaminating endonuclease or exonuclease activity detected. Functionally tested in PCR.
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PfuTurbo DNA Polymerase Alternative Detergent

  • dATP, dCTP and dTTP also available with us..
  • Applications PCR amplification of DNA fragments DNA labeling and DNA sequencing PCR for cloning. Quality Control No contaminating endonuclease or exonuclease activity detected. Functionally tested in PCR.
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dATP100mM, 0.25ML

  • dATP, dGTP and dTTP also available with us..
  • Applications PCR amplification of DNA fragments DNA labeling and DNA sequencing PCR for cloning. Quality Control No contaminating endonuclease or exonuclease activity detected. Functionally tested in PCR.
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5-Color Set, 2 oz. Each of G,Y,BK,R,BL - Plastic

  • Storage Buffer 20mM Tris-HCl, 1mM DTT, 0.1mM EDTA,100mM KCl 50% glycerol, 0.5%NP40, 0.5%TW20.
  • 10×PCR Buffer 750 mM Tris-HCl (pH 8.8 at 25°C), 200 mM KCl, 50 mM (NH4)2SO4, 15mM MgCl2, 0.5% NP-40.
  • Unit definition One unit is the amount of enzyme required to catalyze the incorporation of 10 nmol of nucleotides into acid insoluble material in 30 min. at 74°C under assay conditions..
  • Applications PCR amplification of DNA fragments up to 5 kb DNA labeling and DNA sequencing PCR for cloning. Quality Control No contaminating endonuclease or exonuclease activity detected. Functionally tested in PCR.
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HotStart 2xTaq Pol Master Mix with dye, 5x1 ML, P03-CR03SM-5ML

  • Specialized genetic engineered Taq DNA polymerase enhances the specificity and yield for amplicon.
  • Ready-to-use: Ready-to-use master mix simplifies PCR preparation and minimize the pipetting steps.
  • Hot Start enzyme: Hot Start enzyme design allow user to easily prepare experiments in room temperature, and eliminates nonspecific amplification.
  • Over 5kb DNA: Easy to achieve PCR amplification over 5kb DNA.
  • Best for high throughput: best for high throughput colony PCR to screen desired DNA fragments: with “A” overhang at 3'- end for T/A. cloning use directly.
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