Easy access to products and protocols for research use only in the identification of 2019-nCoV based on Centers for Disease Control and Prevention (CDC) recommendations
So much has changed during this unprecedented time, except your ability to count on Avantor. We continue to set science in motion to create a better world by providing you with the right solutions to keep moving forward.
Our solutions, developed with you as our focus, are crafted by our team and network of professionals with advanced degrees in science, quality control, engineering, manufacturing and industry experience.
Avantor supports end-to-end fluid management solutions – including peristaltic pumps and aseptic fluid transfer solutions – that are reliable and customer-centric, helping bioprocessing manufacturers meet their research and production goals.
A strong, vibrant research and development group is the lifeblood of all industries. VWR will support you from the latest life science products to the guaranteed purity of organic building blocks...
VWR is ready to support your production facility with reliable access to raw materials and essential supplies. We can also help you increase productivity...
VWR is proud of our years of experience providing choice and excellent service to the Industrial market from Food & Beverage, Petrochemical, Environmental Testing, Waste Water, Cosmetics, Consumer Goods, Agriculture and more...
VWR is your complete source for workplace supplies. Binders, calendars, pens, cleaning and sanitation supplies, and office equipment are just some of the essential products we offer...
New Avantor® J.T.Baker® premium conductive and non-conductive robotic tips deliver superior quality and reliable performance for results you can trust.
Avantor Services provides a wide range of specialized services and digital solutions to help you solve complex challenges.
We’ve built our reputation on consistent, comprehensive mastery of day-to-day operations, allowing lab, clinical, and production environments to focus their high-value resources on core scientific priorities.
As our customers’ needs have evolved, so have our capabilities. We have become experts in scientific operations, improving performance with sophisticated solutions and providing guidance on best practices.
You can select and customize services for peak efficiency, quality, and accelerated innovation.
Description:
The new BAC-Optimized Replicator* Electrocompetent Cells (>4x1010 cfu/ug) offer superior genetics and maximum recombinant yields in BAC cloning. 12 reactions.
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MasterAmp* Tth DNA Polymerase, A thermostable DNA- and RNA-dependent (Reverse transcriptase) DNA polymerase for both PCR and RT-PCR applications, Enables amplification of DNA and RNA targets containing high degree
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E. cloni* EXPRESS BL21(DE3) Electrocompetent Cells (? 5 x 109 cfu/ug) are perfect for everyday protein expression and offer the best value available from any supplier. Packaged in two transformations per tube (DUOs) for convenience. 24 rxns.
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E. cloni* 10G ELITE Electrocompetent Cells (>2 x 1010 cfu/¦g) provide large numbers of transformants, even from hard-to-clone or limited DNA. Packaged in two transformations per tube (DUOs) for convenience. 24 rxns.
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EZ-Tn5* Transposase, Create custom transposomes for in vitro transposomics, ntegrate selectable markers, promoters or replication origins into DNA in vitro with EZ-Tn5 insertion kits, random insertion of a EZ-Tn5, genomic DNA of living bacteria, Size: 10 Units
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FailSafe* Enzyme Mix Only, PCR System provides consistent high-fidelity PCR results for every DNA template, PCR amplification of difficult or high-GC templates, Robust amplification of targets up to 20 kb long, Multipl
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RNase I E. Coli, Remove unwanted RNA by digesting with this heat labile, non-sequence specific ribonuclease, with dilution buffer, 10X TNE buffer, and 0.1 M DTT, RNase protection assays to detect single-basepair mismatches in
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CircLigase* II ssDNA Ligase, ATP-independent, non-catalytic thermostable ligase that catalyzes the intramolecular ligation, Intramolecular Epicentre Productligation of single-stranded DNA ends containing 5'-phosphat
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The Nxseq* Ht Dual Indexing Kit Is Required For The Construction Of DNA Fragment Libraries Using The Nxseq Ultralow Kit, 96 Reactions, This Kit Dual Indexing Primers Required For The Construction Of 96 Libraries With Unique Dual Indices, Size: 96 Reactions.
Description:
LavaLAMP* DNA Component Kit with Dye, Contain: 10X LavaLAMP* DNA Buffer, DNA Enzyme, Magnesium Sulfate, 100 mM, DNA Positive Control LAMP Primer Mix and DNA Positive Control, with Green Fluorescent Dye for detection of amplified DNA, Size: 500 reactions
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Lavalamp RNA Component Kit, Enables Sensitive and Fast, Loop-Mediated Isothermal Amplification (Lamp) of Specific RNA Target Sequences from RNA Samples. Using This Kit, Amplified Products Are Detectable Using Non-Fluoresent Met
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Exo-Minus Klenow DNA Polymerase (D355A, E357A), is a DNA-dependent DNA polymerase that lacks both the 5' to ;3' and 3' to ;5' exonuclease activities of E. Coli DNA Polymerase I, Synthesize DNA fr
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NxSeq* AmpFREE Low DNA Library Kit generates DNA fragment libraries for use on Illumina sequencers. Requires only 75 ng of sheared DNA and produces greater sequencing depth and coverage per library in both single and multiplexed sequencing runs. 48 reactions
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Ampligase* DNA Ligase, for applications where ligation at high temperature is beneficial, High thermostability allows ligation using high-stringency hybridization condition, High specificity and stringency permits sensi
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Deliver 2 x 1010 cfu/µg. TG1 high-efficiency electrocompetent cells are suitable for general cloning, ssDNA phage display, M13 phage work, blue/white screening and protein expression.
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OmniCleave* Endonuclease, for Removal of nucleic acids from cell lysates (viscosity) for improved handling and yield of protein preparations, Trace contamination by nucleic acids in protein preparations, host DNA fr
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FailSafe* PCR 2X PreMix I, for PCR amplification of difficult or high-GC templates, Multiplex PCR compatible, Robust amplification of targets up to 20 kb long, PCR System provides dependable, high-fidelity PCR results wi
Description:
CircLigase* II ssDNA Ligase, ATP-independent, non-catalytic thermostable ligase that catalyzes the intramolecular ligation, Intramolecular Epicentre Productligation of single-stranded DNA ends containing 5'-phosphat
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Versatile and useful in a wide variety of applications including routine cloning, subcloning and plasmid isolation with or without blue/white screening. 12 reactions.
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Ampligase* 10X Reaction Buffer, High specificity and stringency permits sensitive detection of SNPs11, igase catalyzes NAD-dependent ligation of adjacent 3'-hydroxylated and 5'-phosphorylated termini in duplex DNA stru
Description:
E. cloni* EXPRESS BL21(DE3) Chemically Competent Cells (? 1 x 107 cfu/ug) are perfect for everyday protein expression and offer the best value available from any supplier. Packaged in two transformations per tube (DUOs) for convenience. 24 rxns.
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TE Buffer, Standard buffer for storing nucleic acids (10 mM Tris-HCl [pH 7.5], 1 mM EDTA), reagent is designed for use with the MasterPure* kit protocols only, Size: 70 ml
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TransforMax* EC100* Electrocompetent E. Coli, 20 Electroporation, Each is supplied with 10 ul (100 pg/ul) of pUC19 Control DNA in TE Buffer, ideal for most cloning applications, Cells provide very high transformation efficiency, Size: 10x100ul
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MMLV High Performance Reverse Transcriptase, Optimized reverse transcriptase and buffer system for the production of full-length cDNA, Amplify first-strand cDNA from picogram amounts of total RNA, Optimize the RT reaction, Size: 25,000 Units
Description:
A DsDNA Binding, Green Fluorescent Dye That Can Be Purchased Separately DNA And Used In Conjunction With The And Rna Master Mixes Or Lavalamp DNA And Rna Component Kit Do Not Include Dye To Fluorescent Detection Of Lamp-Generated Amplification, Size: 200 Reactions.
Description:
Exonuclease VII, Highly specific digestion of ssDNA with both 5' to 3' and 3' to 5' exonuclease activities, Remove Epicentre Product single-stranded oligonucleotide primers after PCR, Minimize the effect of primers left over fro
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