Anti-Perforin (Pore Forming Protein) (Apoptosis Marker) Monoclonal Antibody (Clone: SPM434)
Perforin is a pore-forming protein that leads to osmotic lysis of the target cells and subsequently enables granzymes to enter the target cells and activate apoptosis. Perforin has structural and functional similarities to complement component 9 (C9) . Like C9, this protein creates transmembrane tubules and is capable of lysing non-specifically a variety of target cells. It is one of the main cytolytic proteins of cytolytic granules, and is known to be a key effector molecule for T-cell- and natural killer-cell-mediated cytolysis. Defects in this gene cause familial hemophagocytic lymphohistiocytosis type 2 (HPLH2), a rare and lethal autosomal recessive disorder of early childhood. The expression of perforin is reportedly upregulated in activated CD8+ T-cells, natural killer cells and some CD4+ T-cells.
Product Specifications
Product Name Alternative
Cytolysin; FLH2; HPLH2; Lymphocyte pore-forming protein; PRF1 (pore forming protein 1) ; Perforin-1; PFP; PGFL; PIGF; PIGF-2; PLGF
Gene Name
PRF1
Gene ID
5551
UniProt
P14222
Host
Mouse
Reactivity
Human
Immunogen
Recombinant human Perforin protein fragment (around aa 413-552) (exact sequence is proprietary)
Clonality
Monoclonal
Clone
SPM434
Applications
ELISA
Components
Storage Conditions
Antibody with azide - store at 2 to 8°C. Antibody without azide - store at -20 to -80°C. Antibody is stable for 24 months. Non-hazardous.
Applications Notes
ELISA (For coating, order Ab without BSA)
Isotype
Mouse IgG, kappa
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