Overview
GeneOn: short description for all products
| 3D Transfection |
| Latest transfection 3-D Matrix reagent for studying tissue engineering, tissue regeneration, tumor invasion, neural differentiation, cellular polarization, tissue formation, colonization, neurite growth |
| 3D-Transfect Reagent |
| The transfection reagent is developed to directly transfection of cultured cells in 3D scaffold |
| 3D-PLUS Transfect reagent |
| 3D transfection reagent is developed for directly transfection of cultered cells in all types of hydrogel |
| DNA Transfer Reagents |
| Specialized transfection reagents from GeneON are designed according to the nucleic acids to be delivered and the cell types used in order to achieve optimal efficiency |
| InsectFect Reagent |
| For efficient and reproducible transfection of insect cells. |
| VeroTrans |
| For the transfection of Vero Cells; for many applications such as stable and transient transfection, protein and viral production |
| TransFect Plus Reagent |
| Transfecting from all types of nucleic acids with a very high efficiency |
| EcoFection Reagent |
| Economical transfection - for routine assays and easy cells |
| siRNA Transfer |
| siRNA transfection reagent is ideal for gene silencing. It is a very efficient reagent leading to exceptional knockdown effects with low doses of siRNA. |
| Protein Delivery Systems |
| Innovative reagents allowing intracellular delivery of biologically active proteins or antibodies |
| Antibody Delivery Reagent |
| The transaction reagent forms non-covalent complexes with antibodies through electrostatic and hydrophobic interactions |
| Protein Delivery Reagent |
| The novel transfection reagent allows studying of specific protein functions, protein localization, enlightening new molecular mechanisms |
| LS-ProteinTrans Reagent |
| Large-Scale transient transfection for high protein production yield with reproducible results |
| Transfection Reagent |
| 3-Step transfection reagent with high transfection rate and low Cytotoxicity |
| PCR-Plates 96-Wells |
| PCR Plates and foils for PCR and realtime PCR |
| FrameStar® 96 PCR Plate for LC 480 |
| Compatible with Light Cycler 480, includes 50 films |
| 96-well PCR Plate unskirted |
| PCR plate suitable for most of 0,2 ml Cycler-blocks |
| 96-well PCR Plate unskirted, low profile |
| PCR-Plate with shorter wells |
| 96-well PCR Plate full skirted, low profile |
| Fits to Megabace sequencer and robotic systems |
| 96-well PCR Plate semi-skirted |
| Segmented design, space for bar-coding |
| 96-well PCR Plate, rigid-semi skirted, ABI |
| PCR plate-96 optimized for robotic handling |
| 96-well PCR-Plate adhesive film |
| Thick acrylic layer with superior sealing properties |
| Real-time-PCR adhesive film |
| Ultra clear and flexible adhesive film, especially for LC480 |
DNA/RNA Purification:
| Bacterial DNA purification |
| The isolation kit for bacterial genomic DNA: fast, reliable ... when quality counts ... |
| Tissue DNA Purification |
| The Tissue DNA Extraction Kit is designed for rapid and efficient purification of genomic DNA from up to 5 x 106 cultured animal cells and various organs such as kidney,heart, lungs, brain, muscles, liver, spleen |
| Plant DNA Purification |
| The Plant DNA Extraction Kit is designed for rapid and efficient purification of genomic DNA from a variety of plant tissues without the need for precipitation or organic extraction. |
| Blood DNA Purification |
| The GF-1 Blood DNA Extraction Kit is designed for rapid and efficient purification of genomic DNA from up to 400 µl whole blood. This kit uses a specially treated glass filter membrane fixed into a column to efficiently bind DNA in the presence of high salt |
| Food DNA Purification |
| The Food DNA Extraction Kit is designed for rapid and efficient purification of genomic DNA from up to 100mg of raw or processed food from plant, animal or mixed origins |
| Plasmid DNA Purification |
| The Plasmid DNA Extraction Kit is designed for rapid and efficient purification of high copy and low copy plasmid DNA from bacterial lysates |
| Ambi Gel/PCR Purification |
| AmbiClean Kit (Gel & PCR) is a system designed for DNA recovery from agorose gel and rapid PCR clean-up of DNA bands ranging from 100bp to 20kb |
| PCR Clean-up Purification |
| The PCR Clean Up Kit is a system designed for rapid clean up of DNA bands ranging from100bp to 20kb |
| Gel Extraction Kit |
| The Gel DNA Extraction Kit is a system designed for rapid purification of DNA bands ranging from 100bp to 10kb from all grades of agarose gel in TAE (Tris-acetate/ EDTA) or TBE (Tris-borate/ EDTA) buffer |
| Total RNA Extraction Miniprep |
| The Total RNA Extraction Kit is designed for the isolation of total RNA (longer than 200 bases) from a variety of sources such as animal tissues, bacteria cells and cell cultures |
| Total RNA Blood extraction Miniprep |
| The Total RNA Extraction Kit is designed for the isolation of total RNA (longer than 200 bases) from up to 1ml fresh or frozen anti-coagulated whole blood |
| Viral Nucleic Acid Extraction Kit |
| The Viral Nucleic Acid Extraction Kit is designed for rapid and efficient purification of viral DNA/RNA from samples |
Master Mixes for realtime qPCR: Overview
| qPCR-Master Mixes colorless |
| qPCR Master mixes without internal reference for real time PCR or Hot-Start PCR |
| SuperHot qPCR Master Mix RT |
| qPCR Mastermix for quantification with Sybr green or probes |
| SuperHot qPCR Master Mix HY |
| PCR Master mix for Real time and Hot-Start PCR, optimized for "HIGH YIELD" PCR results |
| SuperHot qPCR Master Mix HS |
| PCR Master mix for Real time and Hot-Start PCR, optimized for "HIGH SPECIFICITY" |
| qPCR-Master Mixes Eva |
| All Master mixes contain EvaGreen as DNA binding dye |
| Real-time-PCR Master Mix E1 |
| qPCR/RTD-PCR Master mix with EvaGreen and dUTP |
| Real-time PCR Master Mix E2 |
| The master mix for RTD-PCR/qPCR contains: EvaGreen, dUTP and UNG |
| Real-time PCR Master Mix E3 |
| The Master mix for RTD-PCR/qPCR contains: EvaGreen, dUTP and ROX (500 nM) |
| Real-time PCR Master Mix E4 |
| The Master mix for RTD-PCR/qPCR contains: EvaGreen, dUTP. UNG and ROX (500 nM) |
| qPCR-Master Mixes DLP |
| qPCR Master mixes DLP safe line: The contamination protector |
| qPCR/real-time-PCR Master Mix DLP1 |
| qPCR/RTD-PCR Master mix with dUTP |
| qPCR/real-time PCR Master Mix DLP2 |
| The master mix for RTD-PCR/qPCR contains: dUTP and UDG |
| qPCR/real-time PCR Master Mix DLP3 |
| The Master mix for RTD-PCR/qPCR contains: dUTP and ROX (500 nM) |
| qPCR/real-time PCR Master Mix DLP4 |
| The Master mix for RTD-PCR/qPCR contains: dUTP. UNG and ROX (500 nM) |
| Polymerases |
| Polymerases for Hot Start PCR (qPCR), Standard PCR and proof-reading (high-fidelity) PCR |
| DFS-Taq DNA Polymerase DNA-free |
| Tag DNA 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 |
| Taq DNA Polymerase |
| Maximo Tag DNA Polymerase is a highly purified polymerase for routine amplification |
| Taq DNA Polymerase 2X-preMix |
| 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 DNA Polymerase blue ready-to-load |
| 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! |
| m-Superhot Taq DNA pol. |
| M-Superhot Taq DNA Polymerase is developed to enhance the specificity, sensitivity and yield of DNA amplification. The enzyme provides a convenient setting up at room temperature |
| p-Superhot Taq DNA pol. |
| p-Superhot Taq DNA 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 |
| Pfu/Psp DNA Polymerase |
| 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 RTL |
| 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 |
| 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 |
| 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. |
PCR Mastermixes / 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 |
| Taq DNA Polymerase 2X-preMix |
| 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 |
| 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! |
| Taq DNA Polymerase 2X-preMix Blue |
| Maximo Tag DNA Blue as 2X-preMix includes all components (Taq DNA polymerase, dNTPs, MgCl2, and reaction buffer) in an optimal concentration for routine PCR. In addition blue dye and loading buffer ensure a direct loading to the agarose gel |
| Pfu/Psp red RTL |
| 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 |
| 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 |
| dNTP´s from GeneOn are available in sets of 4 single dNTPs or as 10 mM ready-to-use mixes |
| dNTP Set / pre-Mixture |
| dNTP´s from GeneOn are available in sets of 4 single dNTPs or as 10 mM ready-to-use mixes |
Reverse Transcription |
| Reverase transcription with AMV or MMLV can uses either RNA or DNA to prime DNA synthesis |
| MMLV Reverse Transcription |
| MMLV Reverse Transcriptase, 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 Transcription |
| 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 |
| Ribunuclease Inhibitor |
| RNase Inhibitor is a recombinant human placental protein which specifically inhibits ribonucleases (RNases) A, B and C |
| Tth DNA Polymerase |
| 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. |
Enzymes/chemicals for PCR |
| Assorted products for PCR and finechemicals for Molecular Biology |
| Uracil-DNA Glycosylase |
| Uracil-DNA Glycosylase (UDG) prevents carry over of DNA in PCR reactions |
| T 4 DNA Ligase |
| 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 50bp-50kbp |
| Universal Agarose from GeneON 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 |
| 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 |
| 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 |
| X-Gal: On combination with suitable bacterial cloning vectors, host strains, |
Light Cycler Capillaries |
| Light Cycler Capillaries from optical Polycarbonate is a clever alternative to the Glas-capillary |
| DNA Ladder/Marker |
| DNA Markers are supplied in ready-to-load, with separate dye or without dye. The ladders allow sizing and concentration estimates of DNA fragments on agarose gels generated by PCR or restriction digest |
| DNA Ladder 10 bp |
| DNA-Ladder Ultra LowRange for electrophoretic analysis of small DNA fragments on high percentage agarose and polyacrylamide gels |
| DNA Ladder 50 bp |
| DNA Marker 50 bp is designed for use as molecular weight standard for agarose gel electrophoresis |
| DNA Ladder 50 bp ready-to use |
| DNA ladder 50 bp from GeneON is containing Orange G & Xylene cyanol FF as tracking dyes |
| DNA Ladder - one for all |
| This DNA Marker offers a unique number of fragments from 100 bp up to 10 kb |
| DNA Ladder 100 bp |
| DNA Marker 100 bp is designed for use as molecular weight standard for agarose gel electrophoresis |
| DNA Ladder 100 bp PLUS BLUE |
| DNA Ladder 100 bp PLUS BLUE (Ready-to-use) is designed for use as molecular weight standard for agarose gel electrophoresis |
| DNA Ladder 100 bp PLUS |
| DNA Ladder 100 bp PLUS is designed for use as molecular weight standard for agarose gel electrophoresis |
| DNA Ladder 1000 bp / 1 kb BLUE ready-to-use |
| DNA BLUE Marker 1000 bp / 1 kb is designed for use as molecular weight standard for agarose gel electrophoresis |
| DNA Ladder 1000 bp / 1 kb |
| DNA Marker 1000 bp / 1 kb is designed for use as molecular weight standard for agarose gel electrophoresis |
| DNA Ladder XXL WideRange, ready-to-use |
| DNA-Ladder UltraWideRange for electrophoretic analysis of small DNA fragments on high percentage agarose and polyacrylamide gels |
| RNA Ladders |
| RNA ladders: For sizing and quantification of single-stranded RNA GeneON offersRNA Ladders covering two different separation ranges: 100-1000 b and 200-6000 b |
| RNA Ladder LowRange |
| RNA Ladders from GeneOn are ideal for sizing and quantification of single-stranded RNA fragments |
| RNA Ladder HighRange |
| RNA Ladders from GeneOn are ideal for sizing and quantification of single-stranded RNA fragments |
| RNA Ladder LowRange ready-to-use |
| RNA Ladders from GeneOn are ideal for sizing and quantification of single-stranded RNA fragments |
| RNA Ladder HighRange ready-to-use |
| RNA Ladders from GeneOn are ideal for sizing and quantification of single-stranded RNA fragments |
Protein Marker/Ladder |
| Protein Markers/Ladders from GeneON are ideal for precise band sizing by SDS-PAGE. They are suited for proteins between 10 und 260 kDa. The proteins can be visualized by Coomassie staining. |
| Protein Marker US7 |
| Protein Molecular Weight Marker US7 (unstained) is ideal for precise sizing of proteins by SDS-PAGE |
| Protein Marker PS10 |
| Protein Molecular Weight Marker PS10 (prestained) is ideal for precise sizing of proteins by SDS-PAGE and for Western blotting. Fits to all buffer systems: Tris-Glycine, MOPS and MES |
| Protein Marker PS11 |
| Protein Molecular Weight Marker PS11 (prestained) is ideal for precise sizing of proteins by SDS-PAGE and for Western blotting. Fits to all buffer systems: Tris-Glycine, MOPS and MES |
| Protein Marker XXL DeLuxe |
| Protein Molecular Weight Marker XXL DeLuxe (prestained) is ideal for precise sizing of proteins by SDS-PAGE and for Western blotting |
DNA Sizer/Marker Classic |
| DNA Sizers/Markers from GeneON are ideal for qualitative and approximate quantitative analysis of dsDNA on agarose gels |
| Phage Lambda DNA Hind III digest ready-to-use |
| DNA Sizer: Phage Lambda Hind III is ideal for qualitative and quantitative analysis of dsDNA |
| Phage Lambda DNA EcoRI digest ready-to-use |
| DNA Sizer: Phage Lambda DNA EcoRI is ideal for qualitative and quantitative analysis of dsDNA |
| Phage Lambda DNA EcoRI/HindIII digest ready-to-use |
| DNA Sizer: Phage Lambda DNA EcoRI/HindIII is ideal for qualitative analysis of dsDNA |
| Phage Lambda DNA StyI digest ready-to-use |
| DNA Sizer: Phage Lambda DNA StyI is ideal for qualitative analysis of dsDNA |
| Phage Lambda DNA PstI digest ready-to-use |
| DNA Sizer: Phage Lambda DNA PstI is ideal for qualitative analysis of dsDNA |
| Phage Lambda DNA BstII digest ready-to-use |
| DNA Sizer: Phage Lambda DNA BstII is ideal for qualitative analysis of dsDNA |
| pBR322 DNA/Hinf I digest ready-to-use |
| DNA Sizer: pBR322 DNA/Hinf I digest is ideal for qualitative analysis of dsDNA |
| pUC19 DNA/BsiS I (Hpa II) digest |
| DNA Sizer: pUC19 DNA/BsiS I (Hpa II) digest is ideal for qualitative analysis of dsDNA |
Cloning Vectors / Phagen DNA |
| Phage and Cloning Vectors are used as a substrate in restriction enzyme activity assays and for preparation of DNA molecular weight standards |
| pBR322 cloning vector |
| pBR322 is a commonly used plasmid cloning vector in E. coli |
| pUC18 DNA |
| pUC18 is a commonly used plasmid cloning vector in E. coli. |
| Phage T7 |
| T7 DNA is an alternative to Lambda DNA for the restriction endonucleases |
| Phage Lambda DNA |
| Phage Lambda DNA is used in restriction enzymes research and for testing of restriction endonucleases activity. |
Spin columns Maxima |
| Spin columns Maxima is a separation system especially developed for use in purification, isolation and separation |
| Filtertips Maxima LOW retention |
| Filtertips Maxima offer a low retention feature. Maxima Filtertips significantly reduce the amount of remaining liquide bound by the tip. The new developed polymers reduces by more than 70 % the deviation of the retained volume. |
| Gel loading tips |
| Gel loading tips and filtertips feature LOW retention. The round tips are especially designed for SDS-page and can be used for Agarose gels. |
| Microplates with Filter |
| Microplates are used in purification, isolation and separation of biomolecules, particularly DNA/RNA. The system includes the Filter-plate and the Receiver-plate (U-bottom) |
| Microplates for Ultrafiltration |
| Microplates for Ultrafiltration are used for: concentration and purification of protein,fractionation of protein, cell broths or other biomolecules. |
| Manifolds for Microplates |
| The manifold for the Maxima (Ultra)Filter-microplates are available for Beckmann, Qiagen robotic systems and as universal standard version |
Restriction Enzymes Alu I |
| Sequence of AluI : 5’…AGCT…3’ 3’…TCGA…5’ |
| ApaL I |
| Sequence of ApaL I: 5´...GTGCAC...3´ 3´...CACGTG...5´ |
| AsuII |
| Sequence of Asu II 5´...TTCGAA...3´ 3´...AAGCTT...5´ |
| BamHI |
| Sequence of BamH I: 5´...GGATCC...3´ 3´...CCTAGG...5´ |
| Bcl I |
| Sequence of BclI: 5´...TGATCA...3´ 3´...ACTAGT...5´ |
| Bgl I |
| Sequence of Bgl I: 5´...GCCNNNNNGGC...3´ 3´...CGGNNNNNCCG...5´ |
| Bgl II |
| Sequence of Bgl II: 5´...AGATCT...3´ 3´...TCTAGA...5´ |
| BseAI |
| Sequence of BseA I: 5´...TCCGGA...3´ 3´...AGGCCT...5´ |
| BseBI |
| Sequence of BseBI: 5´...CC(A/T)GG...3´ 3´...GG(A/T)CC...5´ |
| BseCI |
| Sequence of BseCI: 5´...ATCGAT...3´ 3´...TAGCTA...5´ |
| BshFI |
| Sequence of BshFI: 5´...GGCC...3´ 3´...CCGG...5´ |
| BstEII |
| Sequence of BstEII: 5´...GGTNACC...3´ 3´...CCANTGG...5´ |
| CspAI |
| Sequence of CspA I: 5´...ACCGGT...3´ 3´...TGGCCA...5´ |
| EcoRI |
| Sequence of EcoRI: 5´...GAATTC...3´ 3´...CTTAAG...5´ |
| EcoRV |
| Sequence of EcoRV: 5´...GATATC...3´ 3´...CTATAG...5´ |
| HindIII |
| Sequence of HindIII: 5´...AAGCTT...3´ 3´...TTCGAA...5´ |
| HinfI |
| Sequence of HinfI: 5´...GANTC...3´ 3´...CTNAG...5´ |
| HpaI |
| Sequence of HpaI: 5´...GTTAAC...3´ 3´...CAATTG...5´ |
| KpnI |
| Sequence of KpnI: 5´...GGTACC...3´ 3´...CCATGG...5´ |
| MboI |
| Sequence of MboI: 5´...NGATCN...3´ 3´...NCTAGN...5´ |
| MspCI |
| Sequence of MspCI: 5´...CTTAAG...3´ 3´...CTTAAG...5´ |
| NaeI |
| Sequence of Nae I: 5´...GCCGGC...3´ 3´...CGGCCG...5´ |
| Nco I |
| Sequence of NcoI: 5´...CCATGG...3´ 3´...GGTACC...5´ |
| NheI |
| Sequence of NheI: 5´...GCTAGC...3´ 3´...CGATCG...5´ |
| NotI |
| Sequence of NotI: 5´...GCGGCCGC...3´ 3´...CGCCGGCG...5´ |
| NruI |
| Sequence of NruI: 5´...TCGCGA...3´ 3´...AGCGCT...5´ |
| PstI |
| Sequence of PstI: 5´...CTGCAG...3´ 3´...GACGTC...5´ |
| PvuII |
| Sequence of PvuII: 5´...CAGCTG...3´ 3´...GTCGAC...5´ |
| RsaI |
| Sequence of RsaI: 5´...GTAC...3´ 3´...CATG...5´ |
| SalI |
| Sequence of SalI: 5´...GTCGAC...3´ 3´...CAGCTG...5´ |
| Sau3AI |
| Sequence of Sau3AI: 5´...NGATCN...3´ 3´...NCTAGN...5´ |
| ScaI |
| Sequence of ScaI: 5´...AGTACT...3´ 3´...TCATGA...5´ |
| SfiI |
| Sequence of SfiI: 5´...GGCCNNNNNGGCC...3´ 3´...CCGGNNNNNCCGG...5´ |
| SgrBI |
| Sequence of SgrBI: 5´...CCGCGG...3´ 3´...GGCGCC...5´ |
| SlaI |
| Sequence of SlaI: 5´...CTCGAG...3´ 3´...GAGCTC...5´ |
| SmaI |
| Sequence of SmaI: 5´...CCCGGG...3´ 3´...GGGCCC...5´ |
| SnaBI |
| Sequence of SnaBI: 5´...TACGTA...3´ 3´...ATGCAT...5´ |
| SphI |
| Sequence of SphI: 5´...GCATGC...3´ 3´...CGTACG...5´ |
| SseBI |
| Sequence of SseBI: 5´...AGGCCT...3´ 3´...TCCGGA...5´ |
| SspI |
| Sequence of SspI: 5´...AATATT...3´ 3´...TTATAA...5´ |
| SstI |
| Sequence of SstI: 5´...GAGCTC...3´ 3´...CTCGAG...5´ |
| StyI |
| Sequence of StyI: 5´...CCWWGG...3´ 3´...GGWWCC...5´ |
| TaqI |
| Sequence of TaqI: 5´...TCGA...3´ 3´...AGCT...5´ |
| XbaI |
| Sequence of XbaI: 5´...TCTAGA...3´ 3´...AGATCT...5´ |
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