msdf-1 (cxcl12) (PeproTech)
90
Structured Review
PeproTech
msdf-1 (cxcl12)
Msdf 1 (Cxcl12), supplied by PeproTech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/msdf-1+(cxcl12)/cxcl12+chemokine/pm18230715-28-14-20
Average 90 stars, based on 1 article reviews
Msdf 1 (Cxcl12), supplied by PeproTech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/msdf-1+(cxcl12)/cxcl12+chemokine/pm18230715-28-14-20
Average 90 stars, based on 1 article reviews
msdf-1 (cxcl12) - by Bioz Stars,
2026-10
90/100 stars
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other:Article Title: Identification of in vitro growth conditions for c-Kit-negative hematopoietic stem cells. Article Snippet: Our laboratory recently identified a quiescent class of pluripotent hematopoietic stem cells (PHSCs) that are lineage negative (Linneg), lack c-Kit, and are able to give rise to c-Kit–positive (c-Kitpos) PHSCs in vivo.. This population fails to proliferate in vitro but has delayed reconstituting activity in vivo.. In this study, we purified these cells to enrich for the PHSCs and we identified in vitro conditions capable of supporting their maturation. Article Title: The duffy antigen/receptor for chemokines exists in an oligomeric form in living cells and functionally antagonizes CCR5 signaling through hetero-oligomerization. Article Snippet: The Duffy antigen/receptor for chemokines (DARC) is an unusual chemokine receptor that binds a large number of inflammatory chemokines of both the CC and CXC families with nanomolar affinity, yet it lacks the ability to signal upon ligand binding.. Using bioluminescent resonant energy transfer, we have demonstrated for the first time that DARC exists as a constitutive homo-oligomer in living cells and furthermore that DARC hetero-oligomerizes with the CC chemokine receptor CCR5.. DARC-CCR5 interaction impairs chemotaxis and calcium flux through CCR5, whereas internalization of CCR5 in response to ligand binding remains unchanged. |