| qPCR/real-time-PCR Master Mixes |
| RTD-PCR/qPCR Mastermixes from GeneON are ready to use for RTD-PCR applications. GeneOn offers mixes for dual labeled fluorescent probes and Mastermixes with EvaGreen |
| Polymerases |
| Taq Polymerase for Hot Start PCR (qPCR) and real time PCR, Standard PCR and proof-reading (high-fidelity) PCR |
| one-Fusion high-speed-fidelity Polymerase |
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HighEnd and exclusive Polymerase: faster speed, more accuracy, better result |
| DFS Taq Polymerase DNA-free |
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DFS Taq Polymerase (DNA free) is a highly purified polymerase (DNA-free) especially for PCR reactions where freedom from endogenous template (i.e., E. coli DNA) is essential |
| DFS-PLUS Taq Polymerase DNA-free |
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DFS PlusTaq Polymerase: more sensitivity; more processivity |
| H-SPlus-Taq DNA Polymerase |
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Hot Start Polymerase with ultra short inactivation time, free of MAB´s. The high concentrated versions are designed for Lyophilization |
| Hot-Start PCR: M-Superhot Taq Polymerase |
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Superior Taq Polymerase for Real Time PCR and Hot-Start PCR, low-copy number PCR, PCR of difficult templates, Hot-Start activity (only 5 min initial denaturation). The enzyme is developed to enhance the specificity, sensitivity and yield of DNA amplification. The enzyme provides a convenient setting up at room temperature |
| SNPase for SNP-Genotyping |
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Hot-Start Polymerase for SNP detection by allele-specific PCR and micro sequencing |
| Taq DNA Polymerase |
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Maximo Taq Polymerase is a highly purified polymerase for routine amplification |
| Taq DNA Polymerase 2X-preMix |
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Maximo Tag Polymerase as 2X-preMix includes all components (Taq DNA polymerase, dNTPs, MgCl2, and reaction buffer) in an optimal concentration for routine PCR |
| Taq DNA Polymerase blue ready-to-load |
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Maximo Tag-Blue Polymerase is a highly purified polymerase for routine amplification. The enzyme is ready-to-load. No extra dye or loading buffer is needed! |
| m-Anti-Taq |
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Enhancer for Polymerase reactions |
| p-Taq Polymerase |
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p- Taq Polymerase is developed to enhance the specificity and yield of DNA amplification. The polymerase provides a convenient setting up at room temperature because of blocking the the enzyme with optimized mix of inhibitors |
| Bst DNA Polymerase |
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Bst DNA allows sequencing through problematic secondary structures |
| Pfu/Psp DNA Polymerase |
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Pfu DNA polymerase generated PCR fragments exhibits the lowest error rate of any thermostable DNA polymerases. The fragments are blunt-ended for direct ligation |
| Pfu/Psp red DNA Polymerase RTL |
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Pfu DNA polymerase (RTU=READY-TO-LOAD) is a convenient Mixture of proof-reading Enzyme, red dye and loading buffer. It generated PCR fragments exhibits the lowest error rate of any thermostable DNA polymerases. The fragements are blunt-ended for direct ligation |
| Pfu/Psp DNA Polymerase 2X-preMix |
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Pfu DNA polymerase 2X-preMix is a convenient Mixture of proof-reading Enzyme, reaction buffer dNTP´s and MgCl2. It generated PCR fragments exhibits the lowest error rate of any thermostable DNA polymerases. The fragements are blunt-ended for direct ligation |
| Tth DNA Polymerase |
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Tth DNA Polymerase Maximo is used to reverse-transcribe RNA efficiently in the presence of manganese. PCR can be performed in the same tube using the intrinsic DNA polymerase activity simply by chelation of manganese cation and the addition of magnesium. |
| Standard-PCR Master Mixes / RTU mixes |
| PCR pre-Mixes from GeneOn are convenient in handling, reduce the risk of contamination and pipetting errors but increase the reproducibility. As ready-to-laod (RTL) version the enzymes helps to reduce working time |
| Maximo Dry-Master Mix |
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Ready-to-use lyophilized PCR-Master Mix (Hot-Start) in 8-tubes-strips |
| Taq DNA Polymerase 2X-preMix |
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Maximo Tag DNA as 2X-preMix includes all components (Taq DNA polymerase, dNTPs, MgCl2, and reaction buffer) in an optimal concentration for routine PCR |
| Taq-Blue DNA Pol. ready-to-load |
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Maximo Tag-Blue DNA is a highly purified polymerase for routine amplification. The enzyme is ready-to-load. No extra dye or loading buffer is needed! |
| Pfu/Psp red RTL |
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Pfu DNA polymerase (RTU=READY-TO-LOAD) is a convenient Mixture of proof-reading Enzyme, red dye and loading buffer. It generated PCR fragments exhibits the lowest error rate of any thermostable DNA polymerases. The fragements are blunt-ended for direct ligation |
| Pfu/Psp 2X-preMix |
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Pfu DNA polymerase 2X-preMix is a convenient Mixture of proof-reading Enzyme, reaction buffer dNTP´s and MgCl2. It generated PCR fragments exhibits the lowest error rate of any thermostable DNA polymerases. The fragements are blunt-ended for direct ligation |
| Nucleotides, dNTPs, Primers |
| dNTPs and Nucleotides with highest purity for High-End PCR |
| dNTP Set / dNTP-Mix |
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Nucleotides (> 99 %) are available in sets of 4 single dNTPs or as 10 mM ready-to-use dNTP-mix |
| Biotin-11-dUTP |
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Bio-11-dUTP for non-radioactive DNA labeling |
| Random Primer |
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Mixture of single-stranded random hexanucleotides |
| Oligo (dT)15 |
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Oligo (dT)15 is a standard primer for RT-PCR |
| Reverse Transcription (RT-PCR) |
| RT-PCR: MMLV Reverse Transcriptase, AMV Reverse Transcriptase or Tth DNA Polymerase for the synthesis of cDNA |
| MMLV Reverse Transcriptase |
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MMLV Reverse Transcriptase (for RT-PCR), encoded by Moloney Murine Leukemia Virus (MMLV RT) is an RNA-dependent DNA polymerase that synthesizes the complementary cDNA first strand from a single-stranded RNA template to which a primer has been hybridized |
| AMV Reverse Transcriptase |
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AMV Reverse Transcriptase, encoded by Avian Myeloblastosis Virus reverse transcriptase and expressed in E.coli. is an RNA-dependent DNA polymerase that synthesizes the complementary cDNA first strand from a single-stranded RNA template |
| Ribonuclease (RNase) Inhibitor |
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RNase Inhibitor is a recombinant human placental protein which specifically inhibits ribonucleases (RNases) A, B and C |
| Tth DNA Polymerase |
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Tth DNA Polymerase Maximo is used to reverse-transcribe RNA efficiently in the presence of manganese. PCR can be performed in the same tube using the intrinsic DNA polymerase activity simply by chelation of manganese cation and the addition of magnesium. |
| Random Primers |
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Mixture of single-stranded random hexanucleotides |
| Oligo (dT)15 |
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Standard primer for RT-PCR |
| Enzymes and chemicals for PCR |
| Agarose, UDG Uracil glycosylase, Proteinase K and other assorted products for PCR and finechemicals for Molecular Biology |
| Uracil-DNA Glycosylase |
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Uracil-DNA Glycosylase (UDG) prevents carry over of DNA in PCR reactions |
| T 4 DNA Ligase |
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T 4 DNA Ligase high concentrated catalyzes the formation of a phosphodiester bond between juxtaposed 5´ phosphate and 3´ hydroxyl termini in duplex DNA or RNA. |
| Agarose for gel-electrophoresis |
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Universal Agarose for gel-electrophoresis is ideal for use as standard agarose for analytical as well as preparative nucleic acid electrophoresis of fragments from 50 bp to 50 kbp. Even at low concentrations the gel produced is very firm |
| Proteinase K |
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Proteinase K isolated from Tritirachium album is used for protease digestion during DNA and RNA preparation. Proteinase K from GeneON is very active and stable |
| IPTG |
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IPTG (isopropyl-beta-D-thiogalactopyranoside) is a highly stable synthetic analog of lactose. It is used in conjunction with X-Gal to determine the lac phenotype in blue/white colony screening |
| X-Gal |
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X-Gal: On combination with suitable bacterial cloning vectors, host strains, |
| X-Gluc |
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x-Gluc is a substrate for â-glucuronidase (GUS), an acid hydrolase encoded by the uid A gene |
| Bovine Serum Albumin - BSA |
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BSA prevent the adhesion of enzymes at reaction tubes |
| Light Cycler Capillaries |
| Light Cycler Capillaries from optical Polycarbonate is a clever alternative to the Glas-capillary |
