Human ADP/Acrp30(Adiponectin) ELISA Kit
Human ADP/Acrp30(Adiponectin) ELISA Kit with collaborator-tested sample matrix evidence from Elabscience. Read more ›
["Standard curve"]Product Description
ADP 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: 0.1 ng/mL; standard curve range: 0.16-10 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: Q15848 | NCBI Gene: 9370 | Gene symbol: ADP.
Research Use Only.
Key Facts
| Target | ADP |
| Also known as | ADIPOQ,ACDC,ACRP30,ADIPQTL1,ADPN,APM-1,APM1,GBP28,Adiponectin,Adipocyte,30 kDa adipocyte complement-related protein,Adipocyte complement-related 30 kDa protein (ACRP30),C1q and collagen domain-containing protein,Adipose most abundant gene transcript 1 protein,Gelatin-binding protein |
| Shelf life | 12 months from shipping dates |
| Research area | Cancer, Cardiovascular, Metabolism, Neuroscience, Signal transduction, Stem cells |
| Assay type | Traditional ELISA Kits |
| Detection method | Colorimetric method,ELISA,Sandwich |
| Plate format | 48-well microplate plates pre-coated with anti-ADP 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.