Granzyme B (NK/T-Cell Lymphoma Marker) Antibody, IgG2b, Clone: [GZMB/3014], Mouse, Monoclonal

Catalog Number: NBT-3002-MSM4-B1
Article Name: Granzyme B (NK/T-Cell Lymphoma Marker) Antibody, IgG2b, Clone: [GZMB/3014], Mouse, Monoclonal
Biozol Catalog Number: NBT-3002-MSM4-B1
Supplier Catalog Number: 3002-MSM4-B1
Alternative Catalog Number: NBT-3002-MSM4-B1-0.5,NBT-3002-MSM4-B1-100
Manufacturer: NeoBiotechnologies
Host: Mouse
Category: Antikörper
Application: IHC, WB
Species Reactivity: Human
Immunogen: Recombinant fragment of human GZMB protein (around aa 73-187) (exact sequence is proprietary)
Alternative Names: Cathepsin G-like 1, CCPI, CGL1, CSPB, CTLA-1, CTSGL1, Cytotoxic serine protease B, Cytotoxic T lymphocyte associated serine esterase 1, Cytotoxic T-lymphocyte proteinase 2, Fragmentin-2, GRB, Human lymphocyte protein (Hlp), Lymphocyte protease, SECT, T-cell serine protease 1-3E
Granzyme B is a member of the granule serine protease family stored specifically in NK cells or cytotoxic T cells. Cytolytic T lymphocytes (CTL) and natural killer (NK) cells share the ability to recognize, bind, and lyse specific target cells. They are thought to protect their host by lysing cells bearing on their surface nonself antigens, usually peptides or proteins resulting from infection by intracellular pathogens. Granzyme B is crucial for the rapid induction of target cell apoptosis by CTLs in the cell-mediated immune response. Granzyme B is useful as a marker in the identification of NK/T-cell lymphomas. High percentages of cytotoxic T-cells have been shown to be an unfavorable prognostic indicator in Hodgkins Disease.
Clonality: Monoclonal
Clone Designation: [GZMB/3014]
Molecular Weight: 29-32kDa
Isotype: IgG2b
NCBI: 3002
UniProt: P10144
Form: Antibody purified from Bioreactor Concentrate by Protein A/G and conjugated to Biotin. Prepared in 10mM PBS with 0.05% BSA and 0.05% azide.
Antibody Type: Monoclonal Antibody
Application Notes: Western Blot (2-4ug/ml),,Immunohistochemistry (Formalin-fixed) (2-4ug/ml for 30 minutes at RT),(Staining of formalin-fixed tissues requires heating tissue sections in 10mM Tris with 1mM EDTA, pH 9.0, for 45 min at 95 C followed by cooling at RT for 20 m
SDS-PAGE