MULTI SCIENCES
RUO Human Granzyme K ELISA Kit Plate
RUO Human Granzyme K ELISA Kit Plate
SKU:EK164
Product Details
Brand | MultiSciences |
---|---|
CatNum | 70-EK164 |
Product Name | Human Granzyme K ELISA Kit |
Customs Name | Human Granzyme K ELISA Kit |
Application | ELISA |
Reactivity | Human |
Assay Type | Sandwich ELISA |
Suitable Sample Type | serum, plasma, cell culture supernates |
Format | 96-well strip plate |
Storage | 4℃ (unopened) standard stored at -20℃, others stored at 4℃ (opened) |
Shipping Condition | 4℃ |
Sample Volume | 20 μl |
Sensitivity | 2.41 pg/ml |
Standard Curve Range | 15.63 - 1000 pg/ml |
Spike Recovery Range | 94 % - 107 % |
Mean Spike Recovery | 1 |
CV of Intra plate | 5.5 % - 7.5 % |
CV of Inter plate | 6.8 % - 16.4 % |
Components | 96-well polystyrene microplate coated with a monoclonal antibody against Granzyme K Human Granzyme K Standard, lyophilized Granzyme K Detect Antibody Standard Diluent Streptavidin-HRP Assay Buffer (10×) Substrate (TMB) Stop Solution washing Buffer (20×) Plate Covers |
Describtion | This assay employs the quantitative sandwich enzyme immunoassay technique for the quantitative detection of human Granzyme K. The Human Granzyme K ELISA is for research use only. Not for diagnostic or therapeutic procedures. Granzymes are serine proteases that are released by cytoplasmic granules within cytotoxic T cells and natural killer cells. Their purpose is to induce apoptosis within virus-infected cells, thus destroying them. Granzymes include GranzymeA, Granzyme B, Granzyme H, Granzyme K. Granzyme K is a protein that in humans is encoded by the GZMK gene.This gene product is a member of a group of related serine proteases from the cytoplasmic granules of cytotoxic lymphocytes. Cytolytic T lymphocytes (CTL) and natural killer (NK) cells share the remarkable 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. The protein described here lacks consensus sequences for N-glycosylation present in other granzymes. Granzyme K have been found in high levels of patients who have gone septic. |
