Buffers
Catalog number: EC-887
Size: 10 x 1 ml
- Load more sample per well
- Lithium Dodecyl Sulfate give improved resolution
Quantity discount when you buy 4 or more bottles!
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.
Size: 0.5 ml
- Two Sets of Markers in One
- Prestained Markers Provide Orientation During the Run
- Engineered Molecular Weight Standards Appear in Fluorescent Detection
Size: 1Liter
- DNase and RNase free
- Made with 18 megOhm water
- pH and conductivity optimized
Buffer (MOPS, EDTA & sodium acetate) for RNA electrophoresis. Used as both the tank and gel buffer for denaturing agarose electrophoresis of RNA.
- Reliable and Economical
- 18 Megohm Water
- 0.2 Micron Filtered
Ideal running buffer for high-resolution SDS PAGE of proteins. 20X concentrate makes a working solution of 50mM Tris MOPS, 0.1% SDS and 1mM EDTA.
Quantity discount when you buy 4 or more bottles!
ational Diagnostics’ Neutralization Solution is a ready-to-use sodium chloride-tris buffer solution. It is especially designed for use in Southern and Northern Blotting, and in situ hybridization procedures.
Neutralization Solution contains 3M NaCl and 0.5M Tris in distilled/deionized water.
Catalog Number: CL-253
- Stringent Quality Control Ensures Stability
- Ultra-Pure Reagents in 18 MegOhm Water
- Manufactured with 0.2 Micron Filtration
Size: 450 ml
- Ideal for Western blotting membranes
- Premixed formula saves time, money, and effort
- Stain up to 90 mini blots
Catalog number: EC-886
Size: 10 x 1 ml
- Standard Laemmli Loading Buffer
- Premixed with Bromophenol Blue
- Rigorous Manufacturing Standards Ensure Consistent Results
Size: 1 Liter
- Blot in half the time versus conventional electroblotting buffers
- Very high-efficiency transfer
- Optimal pH; less harsh on proteins
Size: 5 x 1 ml
- Traditional Laemmli Stacking Gel Buffer (4X)
- Formulated with 0.2 Micron Filtration
- Ultra-Pure Reagents in 18 Megohm Water
- Crystal Clear, Reproducible Gels
Catalog number: EC-892
- Traditional Laemmli Resolving Gel Buffer (4X)
- Formulated with 0.2 Micron Filtration
- Ultra-Pure Reagents in 18 MegOhm Water
- Crystal Clear, Reproducible Gels
Size: 200 ml
- Traditional Laemmli Stacking Gel Buffer (4X)
- Formulated with 0.2 Micron Filtration
- Ultra-Pure Reagents in 18 Megohm Water
- Crystal Clear, Reproducible Gels
UreaGel Buffer is one of three components of the UreaGel System. The UreaGel System (formerly SequaGel Sequencing System) consists of UreaGel Concentrate, UreaGel Diluent, and UreaGel Buffer. This system provides a convenient, dependable means for researchers to prepare gels of varying percentage. With the UreaGel System the researcher readily prepares any commonly used gel formulation up to 20% monomer (19:1 Acrylamide/Bisacrylamide). UreaGel Buffer is supplied in 100 ml and 200 ml bottles containing 0.89M tris-borate-20mM EDTA buffer pH 8.3 (10X TBE) and 7.5M urea.
Catalog number: EC-840
UreaGel Diluent is one of three components of the UreaGel System. The UreaGel System (formerly SequaGel Sequencing System) consists of UreaGel Concentrate, UreaGel Diluent, and UreaGel Buffer. This system provides a convenient, dependable means for researchers to prepare gels of varying percentage. With the UreaGel System the researcher readily prepares any commonly used gel formulation up to 20% monomer (19:1 Acrylamide/Bisacrylamide). UreaGel Diluent is supplied in 450 ml and 1 liter bottles containing 7.5M urea in deionized water.
- 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