Human ENPP2 (Ectonucleotide Pyrophosphatase/Phosphodiesterase 2) ELISA Kit
Human ENPP2 (Ectonucleotide Pyrophosphatase/Phosphodiesterase 2) ELISA Kit with collaborator-tested sample matrix evidence from Elabscience. Read more ›
["Standard curve"]Product Description
ENPP2 is the stated analyte for this Elabscience immunoassay kit. The product is listed by ABMIUM using collaborator-supplied specifications for research-use-only quantification workflows.
Assay profile: assay type: Traditional ELISA Kits; detection method: Colorimetric method,ELISA,Sandwich; format: 48Tests.
Performance information: sensitivity: 0.47 ng/mL; standard curve range: 0.78-50 ng/mL; assay duration: 3 h 30 min.
Sample matrix: Elabscience lists Serum, plasma and other biological fluids. These listed sample types are marked C in the ABMIUM sample validation matrix as collaborator-tested ABMIUM Verified evidence. Common unlisted sample types are retained as N where the supplied file does not provide supporting data.
Database references: UniProt: Q13822 | NCBI Gene: 5168 | Gene symbol: ENPP2.
Research Use Only.
Key Facts
| Target | ENPP2 |
| Also known as | ATX,ATX X,Autotaxin,Autotaxin t,ENPP2,E-NPP2,Ectonucleotide pyrophosphatase/phosphodiesterase 2,Ectonucleotide pyrophosphatase/phosphodiesterase family member 2,Enpp2,Extracellular lysophospholipase D,FLJ26803,LysoPLD,NPP2,PD IALPHA,PDNP2,Phosphodiesterase I alpha,Phosphodiesterase I/nucleotide pyrophosphatase 2,Plasma lysophospholipase D |
| Shelf life | 12 months from shipping dates |
| Research area | Immunology |
| Assay type | Traditional ELISA Kits |
| Detection method | Colorimetric method,ELISA,Sandwich |
| Plate format | 48-well microplate plates pre-coated with anti-ENPP2 capture antibody |
Sample Type Validation
1 sample type| Sample Type | SERUM | PLASMA (EDTA) | URINE | CSF | CELL SUPERNATANT |
|---|---|---|---|---|---|
| Human |
Specifications
Storage & Stability
Compliance & Certifications
Manufactured under ISO 9001:2015 quality management standards.
Manufactured under ISO 14001:2015 quality management standards.
Manufactured under ISO 45001:2018 quality management standards.
Not intended for diagnostic or therapeutic use.
Substance does not appear on the SVHC candidate list.