Category: primers

The masking effect of extracellular DNA and robustness of intracellular DNA in anaerobic digester NGS studies

The masking effect of extracellular DNA and robustness of intracellular DNA in anaerobic digester NGS studies

By

On May 23, 2021

In a Cytoscape App., apoptosis, Bacteria, Blocking, Blogging, LUMI-PCR: an Illumina platform ligation-mediated PCR protocol for integration site cloning, Network Diffusion Promotes the Integrative Analysis of Multiple Omics., Pigeon, Plant, plasmid, Plate, plex, Polyclonal, precipitation, Premix, Preps, primers, probe, provides molecular quantitation of integration sites.

Mostly, NGS-based microbiome research are carried out on the whole DNA (totDNA) pool that, nevertheless, consists of extracellular- (exDNA) and intracellular (iDNA) DNA fractions. By investigating the microbiomes of various anaerobic digesters over time, we discovered that totDNA urged decrease species richness contemplating all and/or solely frequent species and yielded fewer distinctive reads as in comparison with iDNA. Moreover, exDNA-derived sequences had been extra just like these from totDNA than from iDNA and at last, iDNA confirmed the perfect efficiency of monitoring temporal adjustments in microbial communities. We postulate that considerable sequences current throughout the exDNA fraction are masking the general outcomes of totDNA and supply proof that exDNA has the potential to qualitatively bias microbiome research no less than within the anaerobic digester surroundings because it incorporates details about cells that had been lysed hours or days in the past.

iDNA, nevertheless, was discovered extra acceptable to realize dependable genetic details about probably alive in addition to uncommon microbes throughout the goal habitat. We in contrast the diagnostic efficiency, turn-around time, and price of those assays. Carbapenemase genes had been outlined utilizing the Carba NP check, modified Carbapenem Inactivation Strategies (mCIM), multiplex PCR, and whole-genome sequencing. We included medical Enterobacterales isolates (n = 36) and nonfermenting gram-negative bacilli isolates (n = 17) collected from 16 acute-care hospitals within the Kinki area of Japan.

Subsequent-generation sequencing (NGS) is broadly used for genome-wide identification and quantification of DNA parts concerned within the regulation of gene transcription. Research that generate a number of high-throughput NGS datasets require knowledge integration strategies for 2 basic duties: 1) technology of genome-wide knowledge tracks representing an combination of a number of replicates of the identical experiment; and a pair of) mixture of tracks from totally different experimental sorts that present complementary data concerning the situation of genomic options reminiscent of enhancers.

 NGS-Integrator is a Java-based command line utility, facilitating environment friendly integration of a number of genome-wide NGS datasets. NGS-Integrator first transforms all enter knowledge tracks utilizing the complement of the minimal Bayes’ issue so that each one values are expressed within the vary [0,1] representing the chance of a real sign given the background noise. Then, NGS-Integrator calculates the joint chance for each genomic place to create an built-in monitor. We offer examples utilizing actual NGS knowledge generated in our laboratory and from the mouse ENCODE database. To forestall the emergence of ceftriaxone resistance in Russia, NG-MAST genotyping should be supplemented with penA allele evaluation.

 

A Easy and Sturdy Enzymatic Fragmentation Methodology for NGS Library Development

A Easy and Sturdy Enzymatic Fragmentation Methodology for NGS Library Development Bin Li (1), James Anderson (1), Ewa Patrycja Malc (2), Piotr Mieczkowski (2), Lin Pham (1) 1 Tecan Genomics, Redwood Metropolis, CA 2 Excessive Throughput Sequencing Facility, Division of Genetics, College of North Carolina, Chapel Hill, USA Subsequent Technology Sequencing strategies have co-evolved with sequencers to work optimally inside a reasonably slender band of DNA fragment lengths. The Illumina methods require fragmenting DNA to a couple hundred base pairs. Bodily shearing strategies, reminiscent of acoustic shearing and sonication, are the commonest DNA shearing strategies.

Sadly, these strategies are laborious, have elevated threat of pattern cross contamination, are tough to automate and the sheared DNA requires restore for adaptor ligation and utility as a template for DNA polymerases. Earlier efforts at using an enzymatic method have i) required titration of enzyme to DNA ii) demonstrated reduce web site bias iii) resulted in a broad fragment size distribution, iv) OR all the above. Right here we current a easy and strong enzymatic methodology to generate random DNA fragments with suitable fragment ends for adaptor ligation.

Tecan’s DNA enzymatic fragmentation methodology is an easy add and incubate workflow that takes about 30 minutes, doesn’t require optimization throughout a variety of enter quantities, gives constant outcomes with out GC bias and is totally automatable. We present reproducible library development on a Tecan automation workstation with constant fragment measurement distribution, and sequencing outcomes of DNA libraries with excessive complexity and low protection bias. This strong and tunable DNA fragmentation methodology means that you can additional simplify your DNA-Seq NGS library preparation workflow.

The masking effect of extracellular DNA and robustness of intracellular DNA in anaerobic digester NGS studies

Molecular Typing of Neisseria gonorrhoeae Medical Isolates in Russia, 2018-2019: A Hyperlink Between penA Alleles and NG-MAST Varieties

This work aimed to review penA gene polymorphisms in medical isolates of Neisseria gonorrhoeae collected in Russia in 2018-2019 and the contribution of the penA allele kind to susceptibility to β-lactam antibiotics. A complete of 182 isolates had been analyzed. penA allele sorts had been decided by sequencing, and the minimal inhibitory concentrations (MICs) of benzylpenicillin and ceftriaxone had been measured. The affect of genetic elements on MICs was evaluated by regression evaluation. All isolates had been prone to ceftriaxone, and 40.1% of isolates had been prone to penicillin.

Eleven penA allele sorts had been recognized. The mosaic kind XXXIV penA allele and the Gly120Lys substitution in PorB made the best contributions to growing the ceftriaxone MIC; the presence of the blaTEM plasmid, Gly120Asp, Ala121Gly/Asn substitutions in PorB, and the adenine deletion within the promoter area of the mtrR gene induced a rise within the penicillin MIC. Amongst 61 NG-MAST sorts recognized, essentially the most frequent had been sorts 228, 807, 9486, 1993, and 6226. A hyperlink between penA alleles and Neisseria gonorrhoeae multi-antigen sequence typing (NG-MAST) sorts was established. Resistance to 2 teams of β-lactam antibiotics was related to non-identical adjustments in penA alleles.

 

Improved Variant Detection in Clinical Myeloid NGS Testing by Supplementing a Commercial Myeloid NGS Assay with Custom or Extended Data Filtering and Accessory Fragment Analysis

Improved Variant Detection in Clinical Myeloid NGS Testing by Supplementing a Commercial Myeloid NGS Assay with Custom or Extended Data Filtering and Accessory Fragment Analysis

By

On April 30, 2021

In a Cytoscape App., apoptosis, Bacteria, Blocking, Blogging, LUMI-PCR: an Illumina platform ligation-mediated PCR protocol for integration site cloning, Network Diffusion Promotes the Integrative Analysis of Multiple Omics., Pig, Pigeon, Plant, plasmid, Plate, plex, Polyclonal, precipitation, Premix, Preps, primers, probe, provides molecular quantitation of integration sites., Visualize omics data on networks with Omics Visualizer

Business myeloid next-generation sequencing (NGS) panels might facilitate uniform era of uncooked information between laboratories. Nevertheless, completely different methods for information filtering and variant annotation might contribute to variations in variant detection and reporting. Right here, we current how customized information filtering or the usage of Oncomine prolonged information filtering enhance detection of clinically related mutations with the Oncomine Myeloid Analysis Assay. The research included all affected person samples (n = 264) analyzed throughout the first-year, single-site, scientific use of the Ion Torrent Oncomine Myeloid Analysis Assay.
In information evaluation, the default evaluation filter was supplemented with our personal information filtering algorithm with a purpose to detect further clinically related mutations. As well as, we developed a delicate supplementary take a look at for the ASXL1 c.1934dupG p.Gly646fs mutation by fragment evaluation. Utilizing our customized filter chain, we discovered 96 completely different reportable variants that weren’t detected by the default filter chain. Twenty-six of those have been labeled as variants of sturdy or potential scientific significance (tier I/tier II variants), and the customized filtering found in any other case undetected tier I/tier II variants in 25 of 132 sufferers with clinically related mutations (19%).
The remaining 70 variants not detected by the default filter chain have been labeled as variants of unknown significance. Amongst these have been a number of distinctive variants with attainable pathogenic potential judged by bioinformatic predictions. The lately launched Oncomine 5.14 prolonged filter algorithm detects most however not the entire tier I/tier II variants that weren’t detected by the default filter. The supplementary fragment evaluation for the ASXL1 c.1934dupG p.Gly646fs confidently detected a variant allele frequency of all the way down to 4.8% (SD 0.83%). The assay additionally detected the ASXL1 c.1900_1922del23 mutation.
Detection of clinically related variants with the Oncomine Myeloid Analysis NGS assay will be considerably improved by supplementing the default filter chain with customized information filtering or the lately launched Oncomine 5.14 prolonged filter algorithm. Our accent fragment evaluation facilitates straightforward testing for frequent ASXL1 mutations which might be poorly or not coated by the NGS assay.

Lowered PCR-generated errors from a hybrid capture-based NGS assay for HLA typing

Subsequent era sequencing (NGS) assays are state-of-the-art for HLA genotyping. To sequence on an Illumina sequencer, the DNA of curiosity should be enriched, fragmented, and bookended with identified oligonucleotide sequences, a course of referred to as library building. Many HLA genotyping assays enrich the goal loci by long-range PCR (LR-PCR), previous to fragmentation. This PCR step has been reported to introduce errors within the DNA to be sequenced, together with inaccurate replication of repeated sequences, and the in vitro recombination of alleles encoded on separate chromosomes.

Another library building technique includes fragmentation of genomic DNA, adopted by hybrid-capture (HC) enrichment of goal HLA loci. This HC-based technique includes PCR, however with far fewer cycles. Consequently, the HC technique had considerably fewer PCR-induced errors, together with extra devoted replication of repeated sequences, and the close to elimination of recombinant sequences. These enhancements possible produce extra correct NGS sequencing information of HLA loci. The Ng-H and Ng’-H contacts vary, actually, between sturdy covalent bonds to weak, non-covalent interactions, and their common variability clearly illustrates the peculiar functionality of the noble gases to bear interactions masking your entire spectrum of the chemical bond.

The construction, stability, and bonding character of fifteen (Ng-H-Ng)+ and (Ng-H-Ng’)+ (Ng, Ng’ = He-Xe) compounds have been explored by theoretical calculations carried out on the coupled cluster stage of idea. The character of the stabilizing interactions was, specifically, assayed utilizing a technique lately proposed by the authors to categorise the chemical bonds involving the noble-gas atoms. The bond distances and dissociation energies of the investigated ions fall in relatively massive intervals, and observe common periodic tendencies, clearly referable to the distinction between the proton affinity (PA) of the varied Ng and Ng’. These variations are properly correlated with the bonding state of affairs of the (Ng-H-Ng)+ and (Ng-H-Ng’)+.

Improved Variant Detection in Clinical Myeloid NGS Testing by Supplementing a Commercial Myeloid NGS Assay with Custom or Extended Data Filtering and Accessory Fragment Analysis

NGS-Based mostly Utility for Routine Non-Invasive Pre-Implantation Genetic Evaluation in IVF

Though non-invasive pre-implantation genetic testing for aneuploidy (NIPGT-A) is probably applicable to evaluate chromosomal ploidy of the embryo, sensible software of it in a routine IVF centre haven’t been began within the absence of a suggestion. Our goal on this research was to offer a complete workflow for a clinically relevant technique for NIPGT-A based mostly on next-generation sequencing (NGS) expertise with the corresponding bioinformatic pipeline. In a retrospective research, we carried out NGS on spent blastocyst tradition media of Day three embryos fertilised with intracytoplasmic sperm injection (ICSI) with high quality rating on morphology evaluation utilizing the clean tradition media as background management.

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Chromosomal abnormalities have been recognized by an optimised bioinformatics pipeline making use of copy quantity variation (CNV) detecting algorithm. On this research, we exhibit a complete workflow masking each wet- and dry-lab procedures supporting a clinically relevant technique for NIPGT-A that may be carried out inside 48 h, which is crucial for the same-cycle blastocyst switch. The described built-in method of non-invasive analysis of embryonic DNA content material of the tradition media can probably complement present pre-implantation genetic screening strategies.

The study of organelle DNA variability in alloplasmic barley lines in the NGS era

The study of organelle DNA variability in alloplasmic barley lines in the NGS era

By

On April 5, 2021

In a Cytoscape App., apoptosis, Bacteria, Blocking, Blogging, LUMI-PCR: an Illumina platform ligation-mediated PCR protocol for integration site cloning, Network Diffusion Promotes the Integrative Analysis of Multiple Omics., Pig, Pigeon, Plant, plasmid, Plate, plex, Polyclonal, precipitation, Premix, Preps, primers, probe, provides molecular quantitation of integration sites., Visualize omics data on networks with Omics Visualizer

Alloplasmic strains are an acceptable mannequin for finding out molecular coevolution and interrelations between genetic programs of plant cells. Complete chloroplast (cp) and mitochondrial (mt) genome sequences had been obtained by the MiSeq System (Illumina). Organelle DNA samples had been ready from a set of 12 alloplasmic barley strains with completely different cytoplasms of Hordeum vulgare ssp. spontaneum and H. vulgare ssp. vulgare, in addition to from their paternal varieties. A bioinformatic strategy for evaluation of NGS information obtained on an organellar DNA combine has been developed and verified.

A comparative research of Hordeum organelle genomes’ variability and disposition of polymorphic loci was performed. Eight forms of chloroplast DNA and 5 forms of mitochondrial DNA had been distinguished for the barley pattern set examined. These outcomes had been in contrast with the earlier information of a restriction fragment size polymorphism (RFLP) research of organelle DNAs for a similar materials. Previously established information a few discipline analysis of alloplasmic barley strains had been revised within the gentle of details about organelle genomes gained after NGS. Completely 17 polymorphic loci had been discovered at exons of chloroplast genomes.

Seven of the SNPs had been situated within the genes of the Ndh complicated. The nonsynonymous adjustments of nucleotides had been detected within the matK, rpoC1, ndhK, ndhG and infA genes. A few of the SNPs detected are very comparable in codon place and in the kind of amino acid substitution to the locations the place RNA modifying can happen. Thus, these outcomes define new views for the long run research of nuclear-cytoplasmic interactions in alloplasmic strains. Roughly 10%, 27%, and 63% of the 540 samples contained < 1500 GE, a variety of 1500-3000 GE, and > 3000 GE, which corresponded to a maximal assay sensitivity of two.0%, 0.5-0.1%, and 0.1-0.05% mutant allelic fraction, respectively.

The sensitivity and specificity had been measured for this BEAMing assay. The variety of mutant beads and mutant allelic fraction had been measured for every EGFR alteration and the extent of detection was established at 0.1% for a median of 2861 genome equal (GE) in every response utilizing HD780 horizon management DNA, in addition to by an inner high quality reference commonplace.  In a routine hospital setting, 11.4% of non-small cell lung most cancers tumors had been constructive at prognosis for EGFR alterations, whereas 43.7% samples harbored EGFR mutations at development, amongst which 40.3% expressed EGFR resistance mutations after first-line tyrosine kinase inhibitor remedy with first- and second-generation medication.

Molecular subtype prognosis of endometrial carcinoma: comparability of NGS panel and ProMisE classifier

The Most cancers Genome Atlas-based molecular classification of endometrial carcinoma (EC) has the potential to higher determine these sufferers whose illness is prone to behave in another way than predicted when utilizing conventional threat stratification, nonetheless, the optimum strategy to molecular subtype task in routine observe stays undetermined. The goal of this research was to check the outcomes of two completely different broadly obtainable approaches to prognosis of EC molecular subtype.
 EC from 60 sufferers, had been molecularly subclassified utilizing two completely different strategies; by performing the FoundationOne CDx Subsequent Technology Sequencing (NGS) panel and utilizing the Proactive Molecular Threat Classifier for Endometrial Most cancers (ProMisE) classifier and performing immunohistochemical stainings for MMR proteins and p53. MSI standing may very well be decided based mostly on the NGS panel ends in 53 of 60 tumors, so ProMisE and NGS molecular subtype task may very well be straight in contrast for these 53 tumors. Molecular subtype prognosis based mostly on NGS and ProMisE was in settlement for 52 of 53 tumors. One tumor was microsatellite steady (MSS) however confirmed lack of MLH1 and PMS2 expression.
 Molecular subtype prognosis of EC based mostly on NGS panel sequencing of formalin-fixed paraffin-embedded endometrial carcinomas and based mostly totally on immunostaining (ProMisE) yield equivalent ends in 98.1% (52/53, kappa – 0.97) of circumstances. Whereas outcomes are comparable utilizing these two approaches, every has benefits and drawbacks that may affect the selection of methodology for use in scientific observe. POLE mutation standing was in each settings derived from FoundationOne outcomes. Molecular classification based mostly on ProMisE was profitable for all 60 tumors.
The study of organelle DNA variability in alloplasmic barley lines in the NGS era

[NGS sequencing in barley breeding and genetic studies]

Barley (Hordeum vulgare L.) is the some of the necessary cereal species used as meals and feed crops, in addition to for malting and alcohol manufacturing. On the finish of the final century, conventional breeding methods had been complemented by means of DNA markers. Molecular markers have additionally been used extensively for molecular genetic mapping and QTL evaluation. In 2012, the barley genome sequencing was accomplished, which supplied a broad vary of recent alternatives – from a extra environment friendly seek for candidate genes controlling economically necessary traits to genomic choice.

The evaluation summarizes the outcomes of the research carried out after barley genome sequencing, which found new areas of barley genetics and breeding with excessive throughput screening and genotyping strategies. Throughout this era, intensive research geared toward identification of barley genomic loci related to economically necessary traits have been carried out; on-line databases and instruments for working with barley genomic information and their deposition have appeared and are being replenished. Lately, GWAS evaluation has been used for large-scale phenotypegenotype affiliation research, which has been broadly utilized in barley since 2010 because of the developed SNP-arrays, in addition to genotyping strategies based mostly on direct NGS sequencing of chosen fractions of the genome.

Standard UV Quartz Cell with Teflon Stopper
SQ014 1 UNIT
EUR 147.24

transilluminator led 20x12 cm + hood
BLOOK ea
EUR 580

Semi-Micro UV Quartz Cell With Frosted Walls and with Teflon Stopper
SQ294 1 UNIT
EUR 171.19

Micro UV Quartz Cell With Lid, Inside Width: 2mm, 0.7ml
SQ244 1 UNIT
EUR 123.3

Micro UV Quartz Cell With Lid, Inside Width: 4mm, 1.4ml
SQ264 1 UNIT
EUR 123.3

Micro UV Quartz Cell With Lid, Inside Width: 5mm, 1.7ml
SQ274 1 UNIT
EUR 123.3

UV TRANSMITTING TRAY
GD-GCS 1/pk
EUR 208
Description: Lab Equipment; Axygen Branded EQ

Fluorescent UV Particles
FP-15040-2 2 mL
EUR 283
Description: Please reffer to the technical data sheet for more detail information for this item. Our dedicated team would be happy to assist you via live chat, email or phone.

uv protected glasses
VLLP70 ea
EUR 99

Semi-Micro UV Quartz Cell With Black Walls And With Lid, Inside Width: 4mm, 1.4ml
SQ024 1 UNIT
EUR 123.3

Semi-Micro UV Quartz Cell With Black Walls And With Lid, Inside Width: 5mm, 1.7ml
SQ144 1 UNIT
EUR 123.3

Semi-Micro UV Glass Cell With Black Walls And With Lid, Inside Width: 4mm, 1.4ml
S024-G 1 UNIT
EUR 104.15

Semi-Micro UV Glass Cell With Black Walls And With Lid, Inside Width: 5mm, 1.7ml
S144-G 1 UNIT
EUR 104.15

SmartDoc UV Blocking Mat
E5000-MAT 1 PC
EUR 100.67

uv lamp 1x15w, 254nm
VL115-C ea
EUR 656

uv lamp 1x15w, 365nm
VL115-L ea
EUR 656

uv lamp 1x15w, 312nm
VL115-M ea
EUR 656

uv lamp 2x15w, 254nm
VL215-C ea
EUR 792

uv lamp 2x15w, 365nm
VL215-L ea
EUR 792

uv lamp 2x15w, 312nm
VL215-M ea
EUR 817

uv lamp 1x6w, 254nm
VL6-C ea
EUR 521

uv lamp 1x6w, 365nm
VL6-L ea
EUR 521

conversion screen uv/blue
VLFC26-BLUE ea
EUR 606

conversion screen uv/wl
VLFC26-WL ea
EUR 606

uv protected face shield
VLMP80 ea
EUR 183

uv protected face shield
VLMP800 ea
EUR 200

UV Carboxyl Particle Array Kit
UVCPAK--5042-14K 14X1 mL
EUR 1278
Description: UltraRainbow Fluorescent Particlesare calibration particles that help you to determine if a flow cytometer is properly aligned and has a clean flow cell with no fluidic blockage. Using SPHERO? Alignment Particles, the coefficients of variation (CVs), peak channels, and histogram distributions can be measured to determine the alignment and functionality of the flow cytometer.

uv lamp 2x15w, 254/365nm
VL215-LC ea
EUR 817

uv lamp 2x15w, 312/365nm
VL215-LM ea
EUR 817

uv lamp 2x15w, 254/312nm
VL215-MC ea
EUR 859

uv lamp 2x6w, 254/365nm
VL6-LC ea
EUR 538

starter uv tube 4w-20w
VLST151 ea
EUR 56

uv table 8w 254nm 15x15 cm
VLECX-15C ea
EUR 1028

uv table 8w 312nm 15x15 cm
VLECX-15M ea
EUR 1028

uv table blue led 20x20 cm
VLECX-20BLUE ea
EUR 1535

uv table 8w 254nm 20x20 cm
VLECX-20C ea
EUR 1113

uv table 8w 365nm 20x20 cm
VLECX-20L ea
EUR 1113

uv table 8w 312nm 20x20 cm
VLECX-20M ea
EUR 1163

uv table 8w, 254nm 21x26 cm
VLECX-26C ea
EUR 1197

uv table 8w, 312nm 21x26 cm
VLECX-26M ea
EUR 1248

uv tube 15 w, 254 nm
VLT15-C ea
EUR 56

uv tube 15 w, 365 nm
VLT15-L ea
EUR 56

uv tube 15 w, 312 nm
VLT15-M ea
EUR 82

uv tube 4 w, 254 nm
VLT4-C ea
EUR 56

uv tube 4 w, 365 nm
VLT4-L ea
EUR 56

uv tube 6 w, 254 nm
VLT6-C ea
EUR 56

uv tube 6 w, 365 nm
VLT6-L ea
EUR 56

uv tube 8 w, 254 nm
VLT8-C ea
EUR 56

uv tube 8 w, 365 nm
VLT8-L ea
EUR 56

uv tube 8 w, 312 nm
VLT8-M ea
EUR 82

Absolute Mag Magnetic Particles, Fluorescent UV
WHM-S135 2 mL
EUR 604

Standard UV Quartz Cell With Lid, 45 X 12.5 X 7.5 mm, Inside Width: 10mm, 1.7ml
SQ003 1 UNIT
EUR 93.5

Standard UV Quartz Cell With Lid, 45 X 12.5 X 12.5 mm, Inside Width: 10mm, 3.5ml
SQ004 1 UNIT
EUR 100.46

Standard UV Quartz Cell With Lid, 45 X 12.5 X 22.5 mm, Inside Width: 10mm, 7.0ml
SQ005 1 UNIT
EUR 128.09

AXYGEN® GEL TRAY 10 X 10 CM FOR USE WITH 10 CM GEL BOX, UV TRANSPARENT
HGB10-10-GT 1/pk
EUR 74
Description: Lab Equipment; Axygen Branded EQ

AXYGEN® GEL TRAY 15 X 10 CM FOR USE WITH 15 CM GEL BOX, UV TRANSPARENT
HGB15-10-GT 1/pk
EUR 79
Description: Lab Equipment; Axygen Branded EQ

AXYGEN® GEL TRAY 15 X 15 CM FOR USE WITH 15 CM GEL BOX, UV TRANSPARENT
HGB15-15-GT 1/pk
EUR 79
Description: Lab Equipment; Axygen Branded EQ

AXYGEN® GEL TRAY 20 X 20 CM FOR USE WITH 20 CM GEL BOX, UV TRANSPARENT
HGB20-20-GT 1/pk
EUR 97
Description: Lab Equipment; Axygen Branded EQ

AXYGEN® GEL TRAY 7 X 10 CM FOR USE WITH 7 CM GEL BOX, UV TRANSPARENT
HGB7-10-GT 1/pk
EUR 68
Description: Lab Equipment; Axygen Branded EQ

AXYGEN® GEL TRAY 7 X 7 CM FOR USE WITH 7 CM GEL BOX, UV TRANSPARENT
HGB7-7-GT 1/pk
EUR 61
Description: Lab Equipment; Axygen Branded EQ

Bacillus cereus UV DNA damage endonuclease (uvsE)
1-CSB-EP467668BQP
  • EUR 611.00
  • EUR 309.00
  • EUR 1827.00
  • EUR 939.00
  • EUR 1218.00
  • EUR 397.00
  • 100ug
  • 10ug
  • 1MG
  • 200ug
  • 500ug
  • 50ug
Description: Recombinant Bacillus cereus UV DNA damage endonuclease(uvsE) expressed in E.coli

WSE-5300 Printgraph CMOS I 6M UV
2305300 1unit
EUR 8510
Description: I ncl udes 312 nm U V t r ansi l l umi nat or , Whi t e L EDl i ght pl at e CE marked

PLT,96WL,UV,NT,NS,25/50
3635 25/pk
EUR 545
Description: Genomics; Genomic Plates

Uv Radiation Resistance Associated Gene (UVRAG) Antibody
20-abx116558
  • EUR 732.00
  • EUR 398.00
  • 150 ul
  • 50 ul

uv table 8w 365/254nm 20x20 cm
VLTCP-20LC ea
EUR 1282

uv table 8w 365/312nm 20x20 cm
VLTCP-20LM ea
EUR 1282

uv table 8w 312/254nm 20x20 cm
VLTCP-20MC ea
EUR 1282

uv table 2x8w, 365/254nm 21x26 cm
VLTCP-26LC ea
EUR 1620

uv table 2x8w, 365/312nm 21x26 cm
VLTCP-26LM ea
EUR 1620

uv table 2x8w, 312/254nm 21x26 cm
VLTCP-26MC ea
EUR 1620

UV excision repair protein RAD23 homolog A Antibody
20-abx110497
  • EUR 411.00
  • EUR 1845.00
  • EUR 599.00
  • EUR 182.00
  • EUR 300.00
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody
20-abx006162
  • EUR 411.00
  • EUR 592.00
  • EUR 182.00
  • EUR 314.00
  • 100 ul
  • 200 ul
  • 20 ul
  • 50 ul

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody
abx030355-400ul 400 ul
EUR 523

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody
abx030355-80l 80 µl
EUR 286

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody
abx030356-400ul 400 ul
EUR 523

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody
abx030356-80l 80 µl
EUR 286

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody
abx030357-400ul 400 ul
EUR 523

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody
abx030357-80l 80 µl
EUR 286

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody
abx030358-400ul 400 ul
EUR 523

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody
abx030358-80l 80 µl
EUR 286

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody
abx448488-100ug 100 ug
EUR 523

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody
abx448489-100ug 100 ug
EUR 523

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody
20-abx313923
  • EUR 411.00
  • EUR 1845.00
  • EUR 599.00
  • EUR 182.00
  • EUR 300.00
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody
abx239352-100ug 100 ug
EUR 509

BioWand Personal UV Sanitizer, 265-280nm, 1/ea
U1001-W 1/pack
EUR 96.58
Description: BioWand Personal UV Sanitizer 265-280nm

uv table 8w 254nm/wl 2x(20x20) cm
VLTFP-CWL ea
EUR 1535

uv table 8w 365nm/wl 2x(20x20) cm
VLTFP-LWL ea
EUR 1535

uv table 8w 312nm/wl 2x(20x20) cm
VLTFP-MWL ea
EUR 1535

One-Step Lumitein UV Protein Gel Stain, 1X
21005-1L 1L
EUR 222
Description: Minimum order quantity: 1 unit of 1L

One-Step Lumitein UV Protein Gel Stain, 1X
21005-4L 4L
EUR 567
Description: Minimum order quantity: 1 unit of 4L

One-Step Lumitein UV Protein Gel Stain, 1X
21005-F 25mL
EUR 50
Description: Minimum order quantity: 1 unit of 25mL

Replacement power supply for nUVaClean UV Pipette Carousel
P5590-PS 1/pack
EUR 76.33
Description: Replacement power supply for nUVaClean UV Pipette Carousel

PhosphoWorks™ Colorimetric MESG Phosphate Assay Kit *UV absorption*
21659 200 Tests
EUR 306

Human UV excision repair protein RAD23 homolog A (RAD23A)
1-CSB-YP019259HU
  • EUR 430.00
  • EUR 234.00
  • EUR 1508.00
  • EUR 642.00
  • EUR 1009.00
  • EUR 291.00
  • 100ug
  • 10ug
  • 1MG
  • 200ug
  • 500ug
  • 50ug
Description: Recombinant Human UV excision repair protein RAD23 homolog A(RAD23A) expressed in Yeast

Human UV excision repair protein RAD23 homolog A (RAD23A)
1-CSB-EP019259HU
  • EUR 380.00
  • EUR 214.00
  • EUR 1309.00
  • EUR 560.00
  • EUR 873.00
  • EUR 262.00
  • 100ug
  • 10ug
  • 1MG
  • 200ug
  • 500ug
  • 50ug
Description: Recombinant Human UV excision repair protein RAD23 homolog A(RAD23A) expressed in E.coli

UV excision repair protein RAD23 homolog A Antibody (Biotin)
20-abx106211
  • EUR 411.00
  • EUR 1845.00
  • EUR 599.00
  • EUR 182.00
  • EUR 300.00
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug

UV excision repair protein RAD23 homolog A Antibody (FITC)
20-abx107625
  • EUR 411.00
  • EUR 1845.00
  • EUR 599.00
  • EUR 182.00
  • EUR 300.00
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug

UV excision repair protein RAD23 homolog A Antibody (HRP)
20-abx109043
  • EUR 411.00
  • EUR 1845.00
  • EUR 599.00
  • EUR 182.00
  • EUR 300.00
  • 100 ug
  • 1 mg
  • 200 ug
  • 20 ug
  • 50 ug

Human UV-Stimulated Scaffold Protein A (UVSSA) ELISA Kit
abx388132-96tests 96 tests
EUR 911

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody (ALP)
abx446398-100ug 100 ug
EUR 578

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody (ALP)
abx446399-100ug 100 ug
EUR 578

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody (APC)
abx446400-100ug 100 ug
EUR 578

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody (APC)
abx446401-100ug 100 ug
EUR 578

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody (Biotin)
abx446402-100ug 100 ug
EUR 578

UV Radiation Resistance-Associated Gene Protein (UVRAG) Antibody (Biotin)
abx446403-100ug 100 ug
EUR 578