TE (Tris EDTA) Buffers, Quality Biological

Supplier: Quality Biological

TE (Tris EDTA) Buffers, Quality Biological

TE (Tris EDTA) Buffers, Quality Biological

TE (Tris EDTA) Buffers, Quality Biological

TE (Tris EDTA) Buffers, Quality Biological

TE (Tris EDTA) Buffers, Quality Biological

TE (Tris EDTA) Buffers, Quality Biological

TE (Tris EDTA) Buffers, Quality Biological

TE (Tris EDTA) Buffers, Quality Biological

TE (Tris EDTA) Buffers, Quality Biological

TE (Tris EDTA) Buffers, Quality Biological

351-011-131 351-011-721 351-010-721 351-322-131 351-010-721EA 351-010-131 351-011-721EA

10128-422EA 61.29 CAD

10128-422 10128-586 10128-420 10128-418 10128-416 10128-414 10128-412

TE (Tris EDTA) Buffers, Quality Biological

Buffers Cloning Buffers

TE is composed of buffering agent Tris, and chelating agent EDTA. EDTA prevents degradation of DNA and RNA by chelating magnesium (or other divalent metal ions). Together, this Tris-EDTA based solution solubilizes DNA or RNA, while protecting it from degradation.

Filtered through a 0.22 µm membrane
DNase, RNnase, and Protease tested

The use of TE with slightly different pH values is based on early 80's literature that DNases are supposed to be less active at pH 8.0 and RNases less active at pH 7.5. You can use pH 8.0 for both DNA and RNA.

TE is useful for reconstituting nucleic acids, during DNA precipitation and other DNA applications, storing and diluting DNA and RNA, breaking protein-links in immuno-histochemistry procedures, and unmasking antigens and epitopes in formalin-fixed and paraffin-embedded tissue sections.

Contents: Tris base, disodium EDTA 2H₂O, hydrochloric acid, and Molecular Biology grade water.

Certifications: Manufactured under a cGMP compliant quality management system in an ISO 9001:2015 certified facility.

Caution: Research use only.

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