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  • Luciferase Cell Lysis Buffer

    Description

    Luciferase Cell Lysis Buffer (LCLB) is a proprietary formulation developed to produce mammalian cell lysates for reporter assays. This lysis buffer is compatible with reagents for assaying the activity of Gaussia as well as other luciferases (e.g. Renilla & Firefly) and β-galactosidase (Figure 1A-D).

    Figure 1: LCLB compatibility with commonly used reporter assay systems. NIH3T3 cells were transfected either with (A) pCMV-GLuc Control Plasmid (NEB #N8081S), (B) a lacZ-expressing vector, (C) a Renilla-expressing vector or (D) a Firefly-expressing vector, using TransPass D2 Transfection Reagent (NEB #M2554S). The supernatants from CMV-GLuc-transfected cells were saved for the assay at 24 h after transfection. All transfected cells were then washed once with PBS (pH 7.4) and lysed with either Luciferase Cell Lysis Buffer or commercially available lysis buffers recommended for each reporter system, respectively. Cell lysates (20 µL out of 100 µL total lysate per sample) were analyzed for GLuc or Renilla luciferase activity using the GLuc Assay Kit (NEB #E3300S/L), β-galactosidase activity using Galacto-Light System (ABI), and Firefly luciferase activity using Luciferase Assay System (Promega). Gaussia luciferase activity was also assayed from the supernatants (20 µL out of 500 µL growth medium of CMV-GLuc-transfected cells per sample).

    Reagents Supplied

    The following reagents are supplied with this product:

    Store at (°C)Concentration
    Luciferase Cell Lysis Buffer45X

    Properties and Usage

    Storage Temperature

    4°C

    Notes

    1. Depending on the cell type, some cells may need larger volume and longer incubation time for sufficient lysis. One can determine whether or not the lysis is sufficient by assaying the activity of intracellular Gaussia luciferase using the pCMV-GLuc Control Plasmid (NEB #N8081). Although the Gaussia luciferase produced from pCMV-GLuc is secreted into the culture medium, at a given time point, 5-10% of the total activity should reside in the lysate (Figure 1A).
    2. Normally, there is no need to remove the cell debris by centrifugation before assaying Gaussia luciferase activity. If additional assays are to be performed (e.g. protein concentration, SDS-PAGE, etc.), it is best to centrifuge the cell lysate to remove cell debris.

    Supporting Documents

    Material Safety Datasheets

    The following is a list of Material Safety Data Sheets (MSDS) that apply to this product to help you use it safely. The following file naming structure is used to name these document files: [Product Name] MSDS. For international versions please contact us at info@neb.com.

    Datacards

    The Product Summary Sheet, or Data Card, includes details for how to use the product, as well as details of its formulation and quality controls. The following file naming structure is used to name the majority of these document files: [Catalog Number]Datasheet-Lot[Lot Number]. For those product lots not listed below, please contact NEB at info@neb.com or fill out the Technical Support Form for appropriate document.
    1. What is the composition of the Luciferase Cell Lysis Buffer?
    2. Can a lysis buffer other than the Luciferase Cell Lysis Buffer be used to make cell lysates for assaying GLuc (or CLuc) acitivity?
    3. Can luciferases other than GLuc and CLuc be assayed from cell lysates made with the Luciferase Cell Lysis Buffer?
    4. Are there differences between cell lines on how fast they can be lysed with the Luciferase Cell Lysis Buffer?
    5. Do I need to remove cell debris in the cell lysate before assaying for GLuc or CLuc activity?
    1. Luciferase Cell Lysis Buffer

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    Application Notes