Ultra Pure Reagents
Catalog Number: EC-603
2-mercaptoethanol is used to cleave disulfide linkages prior to protein electrophoresis. Triple distilled to remove impurities and stored under nitrogen.
Catalog Number: EC-504
Exceeds ACS standards. Low absorbed water results in consistent initiation.
- Small Fragment DNA and RNA
- RT-PCR
- Ultra-Fine particle size for fastest dissolution
- Ultra-High Strength/Low EEO Agarose
- Blotting of MegaBase DNA
- Finest Particle Size for Fastest Dissolution
- High Strength High-Resolution Agarose
- Excellent for small DNA fragments, PCR products, and proteins
- Ultra-Fine particle size for fastest dissolution
- Highest Quality Molecular Biology Grade Agarose
- Low Electroendosmosis
- DNase and RNase free
- Rapidly Dissolving, Low Boil-Over
- Low Melting Temperature
- DNase and RNase free
- Exceptional Gel Strength for a Low Melt Agarose
- Fastest Dissolving
Boric acid is a primary component of TBE buffer, the most commonly used electrophoresis buffer in PAGE of DNA and RNA. Certified DNase and RNase free.
Size: 5 g
Size: 10 g
Size: 10 g
Size: 10 g
N,N’ – diallyltartardiamide
Size: 50 ml
- DNase and RNase free
- Made with 18 megOhm water
- 0.2 micron filtered
Component of hybridization solutions for Northern and Southern blotting. Increases speed and sensitivity of hybridization reactions.
Certified nuclease-free; deionized and autoclaved.
Catalog number: EC-877
Aids information of networks (highly localized concentrations of probes) during hybridization, thus expediting the annealing process.
Molecular Weight | Purity |
500,000 | 99% |
Cleland’s Reagent. Specially purified of trace metals and other impurities.
Disodium ethylenediamintetraacetate dihydrate
Chelating agent added to electrophoresis buffers to preserve sample integrity by disabling certain metal dependant nucleases. Certified DNase and RNase free.
- Using PAGE to Determine Nucleic Acid Molecular Weight
- SSCP Analysis
- Sanger Sequencing
- Sample Preparation for Native PAGE of DNA
- Sample Prep for Denaturing PAGE of DNA
- S1 Mapping
- Run Conditions in Denaturing PAGE
- RNA Mapping
- RNA Electrophoresis
- Ribonuclease Protection
- Restriction Digest Mapping
- Primer Extension
- Preparing Denaturing DNA & RNA Gels
- Preparation of Denaturing Agarose Gels
- Preparation of Agarose Gels
- Pouring Sequencing Gels
- PFGE and FIGE
- PCR Analysis: Yield and Kinetics
- PCR Analysis: An Examination
- Native PAGE of DNA
- Mobility Shift Assay
- Methylation & Uracil Interference Assays
- Maxam & Gilbert Sequencing
- Manual Sequencing
- In Gel Enzyme Reactions
- Heteroduplex Analysis
- Gel Preparation for Native PAGE of DNA
- Gel Electrophoresis of PCR Products
- DNase I Footprinting
- DNA/RNA Purification from PAGE Gels
- DNA/RNA Purification from Agarose Gels – Electroelution
- Differential Display
- Denaturing Polyacrylamide Gel Electrophoresis of DNA & RNA
- Conformational Analysis
- Automated Sequencers
- Analysis of DNA/Protein Interactions
- Agarose Gel Electrophoresis of DNA and RNA – Uses and Variations
- Agarose Gel Electrophoresis of DNA and RNA – An Introduction