
Human CXCL4/PF4 PicoKine ELISA Kit standard curve
Human CXCL4/PF4 ELISA Kit PicoKine(r)
EK0726
Product group Assays
Overview
- SupplierBoster Bio
- Product NameHuman CXCL4/PF4 PicoKine ELISA Kit
- Delivery Days Customer9
- ApplicationsELISA
- Applications SupplierELI
- Assay Detection Range156 pg/ml - 10,000 pg/ml
- Assay Sensitivity<15 pg/ml
- Assay Time15-20
- CertificationResearch Use Only
- Scientific DescriptionHuman CXCL4/PF4 ELISA Kit PicoKine® (96 Tests). Quantitate Human PF4 in cell culture supernatants, cell lysates, serum and plasma (heparin, EDTA). Sensitivity: 15pg/ml. The brand Picokine indicates this is a premium quality ELISA kit. Each Picokine kit delivers precise quantification, high sensitivity, and excellent reproducibility. Only our most reliable and effective kits qualify as Picokine, guaranteeing top-tier results for your assays.
- Reactivity Supplierhuman CXCL4
- Storage Instruction-20°C,2°C to 8°C
- UNSPSC41116158
References
- Lv Y, Yang Z, Hai L, et al. Differential alterations of CXCR3, CXCR5 and CX3CR1 in patients with immune thrombocytopenia. Cytokine. 2024,181:156684. doi: 10.1016/j.cyto.2024.156684Read this paper
- Wang Z, Tenzing N, Xu Q, et al. Apoptosis is one cause of thrombocytopenia in patients with high-altitude polycythemia. Platelets. 2023,34(1):2157381. doi: 10.1080/09537104.2022.2157381Read this paper
- Qin J, Zhang J, Jiang J, et al. Direct chemical reprogramming of human cord blood erythroblasts to induced megakaryocytes that produce platelets. Cell Stem Cell. 2022,29(8):1229-1245.e7. doi: 10.1016/j.stem.2022.07.004Read this paper
- Xu T, Zhao J, Wang X, et al. CXCL4 promoted the production of CD4(+)CD25(+)FOXP3(+)treg cells in mouse sepsis model through regulating STAT5/FOXP3 pathway. Autoimmunity. 2020,53(5):289-296. doi: 10.1080/08916934.2020.1777283Read this paper
- Ren Q, Chan KW, Huang H, et al. Platelet-derived alpha-granules are associated with inflammation in patients with NK/T-cell lymphoma-associated hemophagocytic syndrome. Cytokine. 2020,126:154878. doi: 10.1016/j.cyto.2019.154878Read this paper