踉跄
发表于 2025-3-23 13:16:00
Intrafemoral Delivery of Hematopoietic Progenitorsvironment. As a demonstrative example, we provide a protocol for the isolation of granulocyte–monocyte progenitors (GMP) by cell sorting, the delivery of these cells into recipient animals by intrafemoral transfer, and finally, the analysis of GMP-derived progenies by flow cytometry.
酷热
发表于 2025-3-23 14:50:34
http://reply.papertrans.cn/19/1897/189674/189674_12.png
tenuous
发表于 2025-3-23 20:24:25
Book 2021arrow in both mouse and human. Chapters details methods on bone marrow (BM) ecosystem, to label, sort, analyse, and culture specific cell subsets as well as techniques allowing the evaluation of the function of some of the cellular elements of the BM. Written in the highly successful .Methods in Mol
藐视
发表于 2025-3-23 23:46:33
https://doi.org/10.1007/978-94-017-4851-3nd respiratory capacity in a single experiment. Here we describe the protocol used to study concomitantly the respiratory and glycolytic metabolism of primary MSCs from the determination of oxygen consumption (OCR) and extracellular acidification (ECAR) rates.
蛤肉
发表于 2025-3-24 03:13:06
https://doi.org/10.1007/978-94-010-2770-0tive oxygen species and low mitochondrial activity..Here, we describe the methodology to characterize the physiologic state of HSPCs isolated from their native hematopoietic organ using flow cytometry-based assays. These protocols allow evaluation of their ROS levels and activated signaling pathways under various conditions.
CERE
发表于 2025-3-24 09:46:10
http://reply.papertrans.cn/19/1897/189674/189674_16.png
Isolate
发表于 2025-3-24 10:40:46
http://reply.papertrans.cn/19/1897/189674/189674_17.png
千篇一律
发表于 2025-3-24 18:40:09
Literature and the Authority of Technology,nally, in vitro MSC culture and differentiation into osteoblasts, adipocytes, and chondrocytes will be explained. Thus, this chapter will detail all bases to work on MSC with consensus and clear methods and protocols.
Osteoporosis
发表于 2025-3-24 19:28:14
https://doi.org/10.1007/978-94-017-4851-3s. Here we describe the minimum requirements and an efficient method for isolation, expansion of mouse bone-derived multipotent mesenchymal stromal cells and their differentiation into osteoblasts, responsible for the bone matrix synthesis and mineralization.
澄清
发表于 2025-3-24 23:59:28
https://doi.org/10.1007/978-94-017-4851-3 an original in vitro system allowing to quantify by flow cytometry the differentiation of mouse HSCs into lineage-primed multipotent hematopoietic progenitors (MPPs) in a cytokine-supplemented feeder-free medium.