Perforin ELISpot Assay Kit (Human) (OKDB00025)

Catalog No: OKDB00025

Product Info

• Predicted Species Reactivity: Human
• ELISA Kit Duration: < 4 Hours
• ELISA Kit Principle: Aviva's Human Perforin ELISpot Kit is based on standard sandwich ELISA methodology. A capture antibody highly specific for the analyte of interest is coated to the wells of a PVDF bottomed 96 well microtitre plate either during kit manufacture or in the laboratory. The plate is then blocked to minimise any non-antibody dependent unspecific binding and washed. Cell suspension and stimulant are added and the plate incubated allowing the specific antibodies to bind any analytes produced. Cells are then removed by washing prior to the addition of Biotinylated detection antibodies which bind to the previously captured analyte. Enzyme conjugated streptavidin is then added binding to the detection antibodies. Following incubation and washing substrate is then applied to the wells resulting in coloured spots which can be quantified using appropriate analysis software or manually using a microscope.
• ELISA Kit Component: Reagents sufficient for 96 Wells:
  1. Pre-coated 96 well PVDF bottomed plates (1x96 Wells)
  2. Biotinylated detection antibody
  3. Streptavidin-Alkaline Phosphatase conjugate
  4. Bovine Serum Albumin
  5. Ready to use BCIP/NBT substrate buffer
  
• Reconstitution and Storage: 2 to 8C, Do not use past expiration date.
• Sample Type: Cell Suspensions
• Assay Info: Assay Methodology: Quantitative Sandwich ELISpot Immunoassay

Target Info

• Gene Symbol: Perforin
• Gene Full Name: perforin 1
• Alias Symbols: P1, PFP, HPLH2
• NCBI Gene Id: 5551
• Protein Name: perforin-1
• Description of Target: The protein encoded by this gene 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. This protein is one of the main cytolytic proteins of cytolytic granules, and it 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. Alternative splicing results in multiple transcript variants encoding the same protein.
• Uniprot ID: P14222
• Protein Accession #: NP_001076585.1
• Nucleotide Accession #: NM_001083116.1
• Protein Size (# AA): 555
• Molecular Weight: 61 kDa