Tris-edta

Compare Tool

Select up to 3 products

Tris-edta
1 - 32 of 46
Related Categories: Tris Edta Buffer | Tris Edta
Sort
View
Show
  • Ready to use, sterile TE (Tris-EDTA) buffer solution prepared with 18.2 megOhm water, 0.2 micron sterile filtered and steam sterilized in final packaging. Nuclease free TE is used to solubilize DNA/RNA while providing protection from degradation. It provides great buffering capabilites for…

  • TE Buffer, 10X Powder

    RPI (Research Products International)

    Dry homogeneous blend of molecular biology grade Tris-base and EDTA, disodium salt. For use in gel electrophoresis. Supplied as 158.35 grams of powder which is used to produce a 10X concentrate.

  • Components: Tris Base / Tris-HCl(10 mM), EDTA(1 mM), Water(rest) Method: Prepared in 18.2 megohms-cm ± 1 low endotoxin water and filtered through 0.22-micron filter. pH: 8.0 ± 0.15 Storage: Room Temp.

  • Components: Tris Base / Tris-HCl(200 mM), EDTA Disodium Dihydrate(20 mM) Method: Prepared in 18.2 megohms-cm ± 1 water and autoclaved at 15 psi (121°C) for 30 minutes on liquid cycle and/or filtered through 0.22-micron filter. pH: 8.0 ± 0.15 (1X) Storage: Room Temp.

  • Components: Tris Base / Tris-HCl(10 mM), EDTA(1 mM), Water(rest) Method: Prepared in 18.2 megohms-cm ± 1 water and autoclaved at 15 psi (121°C) for 30 minutes on liquid cycle and/or filtered through 0.22-micron filter. pH: 7.6 ± 0.15 Storage: Room Temp.

  • Tris-EDTA (TE) Buffer

    Corning cellgro

    Tris-EDTA (TE) buffer is commonly used in work with nucleic acids. Examples include as a solubilization buffer in DNA and RNA purification, as a running buffer in electrophoresis, and as a general storage buffer for nucleic acids.

  • Synonym: TE buffer solution EC Number: 231-791-2 MDL number: MFCD00236359

  • Tris-EDTA Buffer (20X)

    Boston BioProducts

    Components: Tris Base / Tris-HCl(200 mM), EDTA(20 mM), Water(rest) Method: Prepared in 18.2 megohms-cm ± 1 water and autoclaved at 15 psi (121°C) for 30 minutes on liquid cycle. pH: 8.0 ± 0.15 (1X) Storage: Room Temp.

  • Components: EDTA(~0.74%), Tris Base / Tris-HCl(~3.2%), Water(rest) Method: Prepared in 18.2 megohms-cm ± 1 water and autoclaved at 15 psi (121°C) for 30 minutes on liquid cycle and/or filtered through 0.22-micron filter. pH: 7.4 ± 0.15 Storage: Room Temp.

  • Synonyms: TE buffer solution Physical form: 10 mM Tris-HCl; 1 mM EDTA

  • STE Buffer, 1X Solution

    RPI (Research Products International)

    Formulation: NaCI: 100 mM TRIS HCI: 10 mM pH 8.0 EDTA: 1 mM

  • Tris-EDTA Common buffer for DNA isolation and electrophoresis protocols

  • Tris-EDTA Buffer (10X)

    Boston BioProducts

    Components: Tris Base / Tris-HCl(100 mM), EDTA(10 mM), Water(rest) Method: Prepared in 18.2 megohms-cm ± 1 water and autoclaved at 15 psi (121°C) for 30 minutes on liquid cycle. pH: 8.0 ± 0.15 (1X) Storage: Room Temp.

  • Tris-EDTA stock solution (TE) buffer contains a concentrated solution of filtered Tris-EDTA (10X, pH 7.4).

  • Components: Tris Base / Tris-HCl(0.2 M), EDTA(20 mM), Water(rest) Method: Prepared in 18.2 megohms-cm ± 1 water and autoclaved at 15 psi (121°C) for 30 minutes on liquid cycle and/or filtered through 0.22-micron filter. pH: 7.6 ± 0.15 (1X) Storage: Room Temp.

  • Components: Tris Base / Tris-HCl(200 mM), EDTA(20 mM), Water(rest) Method: Prepared in 18.2 megohms-cm ± 1 water and autoclaved at 15 psi (121°C) for 30 minutes on liquid cycle and/or filtered through 0.22-micron filter. pH: 7.4 ± 0.15 (1X) Storage: Room Temp.

  • Synonym: TE buffer solution EC Number: 231-791-2 MDL Number: MFCD00236359 Components TE Buffer contains 1M Tris-HCl (pH approximately 8.0), containing 0.1M EDTA. Application Suitable for storage of RNA and DNA, including purified plasmid DNA stocks. General…

  • AccuGENE™Tris- EDTA Buffer is a basic Tris buffer with added EDTA. It is Commonly used as the basis for other buffers such as TAE and TBE, and electrophoresis for DNA/RNA destined for downstream enzymatic processes.

  • STET Buffer, 1X Solution

    RPI (Research Products International)

    Formulation: NaCI: 100 mM TRIS HCI: 10 mM EDTA: 1 mM Triton X-100: 5%

  • Glycine

    IBI Scientific

    Glycine is a neutral amino acid. It is the primary component in polyacrylamide buffers. During the process of separation the glycine forms an electrical front which pulls the macromolecules along. Store at room temperature. Keep tightly sealed. Protect from moisture. Avoid contact to the…

  • TAE 50X Buffer

    RPI (Research Products International)

    Solution contains: Tris (hydroxymethyl) aminomethane: 2 M Acetic Acid: 1 M EDTA, Disodium Salt Dihydrate: 50 mM

  • Tris-EDTA-NaCl Buffer solution at pH 8.0. A customer enquired about this buffer to make as custom and we also added as a new product. Features Precision in concentration and pH Guaranteed reproducibility Applications As a buffering mix

  • Tris-EDTA, 100X, Powder

    Spectrum Chemical

  • Tris-EDTA, 100X Solution

    Spectrum Chemical

  • TE Buffer Solution pH 8.0

    MilliporeSigma

    Formula Weight: CAS Number: Tris: 77-86-1, Boric Acid: 10043-35-3 EDTA: 6381-92-6 Synonym(s): TRIS-EDTA Buffer Description: Each liter of concentrate makes 5L of 1X TBE

  • 0.5M EDTA, pH 8.0

    Quality Biological

    EDTA (Ethylenediaminetetraacetic acid), a metal chelator, is widely used in molecular biology as a chemical reagent to reduce nuclease activity (i.e. metalloenzyme). EDTA solution can be used to study cell biology, molecular biology, bioactive small molecules, biochemicals, solutions and…

  • AccuGENE™ TBE (Tris hydroxymethyl aminomethane) is made from Tris, EDTA and Boric acid. The addition of borate makes TBA a better conductive medium than TAE so it less prone to overheating and better for longer runs. Borate does inhibit some enzymatic reactions, so it is not often used if the…

  • AccuGENE™ TBE (Tris hydroxymethyl aminomethane) is made from Tris, EDTA and Boric acid. The addition of borate makes TBA a better conductive medium than TAE so it less prone to overheating and better for longer runs. Borate does inhibit some enzymatic reactions, so it is not often used if the…

  • Phenol:Chloroform 400ml

    MilliporeSigma

    Formula: Phenol:Chloroform 1:1. saturated TRIS-EDTA buffer:Isoamyl alcohol 25:24:1 Formula Weight: N/A Description: .General Product Use: For DNA Applications Preparation: pH 8.0 0.2: Gently mix contents of phenol:chloroform and buffer bottles. Allow layers to separate before use (2-4…

  • UFC503008

    MilliporeSigma

    …device provides the best balance between recovery and spin time for double-stranded DNA for base pairs ranging from 137 to 1159. To achieve maximum PCR product recovery and primer removal with primers greater than 20 bases, one or two additional spins with Tris-EDTA (TE) buffer are recommended.

Compare Tool

Select up to 3 products

Please Log In

Don't have a web profile? Create one now.