10x Tris-Glycine Native Running Buffer (1L, 4L, 10L)

    Description

    10xTris-Glycine Native Running Buffer is designed for protein gel electrophoresis under native running conditions with Tris-Glycine gels or Tris-Acetate gels.

    Tris-Glycine gels do not contain SDS and can be used to accurately separate both native and denatured proteins, depending upon the sample and running buffers used. To separate denatured proteins on Tris-Glycine gels, use Tris-Glycine SDS Sample Buffer and Tris-Glycine SDS Running Buffer. To separate native proteins use Tris-Glycine Native Sample Buffer and Tris-Glycine Native Running Buffer.

    Composition:

    10xTGS: Tris 250 mM, Glycine 1.92 M, pH 8.3

    Usage Recommendations

    To prepare 1X TG buffer, add 100 ml of 10X TG buffer to 900 ml of deionized water and mix well. 

    Read more

    Product form

    SKU: TG02-1L

    10x Tris-Glycine Native Running Buffer (1L, 4L, 10L)

      10xTris-Glycine Native Running Buffer is designed for protein gel electrophoresis under native running conditions with Tris-Glycine gels or Tris-Acetate gels. Tris-Glycine... Read more

      $30.00

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          MSDS

        Description

        10xTris-Glycine Native Running Buffer is designed for protein gel electrophoresis under native running conditions with Tris-Glycine gels or Tris-Acetate gels.

        Tris-Glycine gels do not contain SDS and can be used to accurately separate both native and denatured proteins, depending upon the sample and running buffers used. To separate denatured proteins on Tris-Glycine gels, use Tris-Glycine SDS Sample Buffer and Tris-Glycine SDS Running Buffer. To separate native proteins use Tris-Glycine Native Sample Buffer and Tris-Glycine Native Running Buffer.

        Composition:

        10xTGS: Tris 250 mM, Glycine 1.92 M, pH 8.3

        Usage Recommendations

        To prepare 1X TG buffer, add 100 ml of 10X TG buffer to 900 ml of deionized water and mix well. 

        Read more

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