Humanized IL-3/GM-CSF knockout mice sustain human hematopoietic cells and form human immune granulomas for pathogen infection studies.
A thrombopoietin-FLT3 ligand fusion polypeptide extends circulation time while boosting platelet production and hematopoietic cell survival.
A staged affinity, mixed-mode, and cation exchange sequence removes sulfide variants from refolded Fc-peptide fusion proteins while preserving yield.
PVA and PI3K activators enable albumin-free, serum-free expansion of human hematopoietic stem cells while maintaining CD34+ populations.
Poor human HSC support limits mouse models; RAG/Il2rg knockouts and humanized cytokines sustain engraftment for immune-response testing.
Isolated MPL ligand resolves thrombocytopenia treatment gaps by enabling precise factor identification and reliable platelet production.
A thermoregulated expression system using a mutant cI857 repressor induces Fc-peptide fusion protein synthesis via mild temperature shifts.
Thrombopoietin mediates megakaryocyte maturation via mpl receptors, resolving inadequate platelet counts in thrombocytopenia.
Recombinant MPL ligand stimulates megakaryocyte proliferation, addressing ineffective glucocorticoid treatments for thrombocytopenia.
TPO-coated scaffolds promote robust bone healing with less heterotopic bone formation than BMP-2.
A dimerized TMP-TMP-HSA fusion protein extends plasma half-life through covalent disulfide bonds formed by a dedicated dimerization domain.