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Your Position: Home > Protein > Granzyme B > GZB-H5213

Human Granzyme B Protein, Tag Free (active enzyme)

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  • Synonym
    GZMB,CCPI,CGL-1,CGL1,CSP-B,CSPB,CTLA1,CTSGL1,HLP,SECT,Fragmentin-2,Granzyme B,Granzyme-2,GRB
  • Source
    Human Granzyme B Protein, Tag Free(GZB-H5213) is expressed from human 293 cells (HEK293). It contains AA Ile 21 - Tyr 247 (Accession # P10144).
    Predicted N-terminus: Ile 21
  • Molecular Characterization
    Granzyme B Structure

    This protein carries no "tag".

    The protein has a calculated MW of 25.5 kDa . The protein migrates as 34-37 kDa when calibrated against Star Ribbon Pre-stained Protein Marker under reducing (R) condition (SDS-PAGE) due to glycosylation.

  • Endotoxin
    Less than 1.0 EU per μg by the LAL method / rFC method.
  • Purity

    >90% as determined by SDS-PAGE.

  • Formulation

    Supplied as 0.2 μm filtered solution in 50 mM Tris, 150 mM NaCl, pH7.5 with trehalose as protectant.

    Contact us for customized product form or formulation.

  • Shipping

    This product is supplied and shipped with dry ice, please inquire the shipping cost.

  • Storage

    Please avoid repeated freeze-thaw cycles.

    This product is stable after storage at:

    1. The product MUST be stored at -70°C or lower upon receipt;
    2. -70°C for 3 months under sterile conditions.
SDS-PAGE
Granzyme B SDS-PAGE

Human Granzyme B Protein, Tag Free on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90% (With Star Ribbon Pre-stained Protein Marker).

Bioactivity

Measured by its ability to cleave the fluorogenic peptide substrate, Ac-Ile-Glu-Thr-Asp-AFC. The specific activity is >140 pmol/min/μg (QC tested).

  • Background
    Granzyme B (GZMB) is a cytosolic protease abundant in cytotoxic T-cells and natural killer cells, pivotal for immune defense. Delivered into target cells, GZMB activates caspase-independent pyroptosis by cleaving gasdermin-E (GSDME). This triggers pyroptosis, leading to target cell death. GZMB exhibits substrate specificity for aspartate residue cleavage and contributes to an activation cascade of caspases, impacting apoptosis execution. Involved in bacterial infection response, GZMB cleaves and activates caspase-7, promoting plasma membrane repair. Its multifaceted activities underscore its crucial role in immune responses and cellular defense.
  • Clinical and Translational Updates

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