نتایج جستجو برای: pellet culture

تعداد نتایج: 285854  

Journal: :Investigative ophthalmology & visual science 2007
Yiqin Du Nirmala Sundarraj Martha L Funderburgh Stephen A Harvey David E Birk James L Funderburgh

PURPOSE To investigate the potential of human corneal stromal stem cells to assume a keratocyte phenotype and to organize extracellular matrix (ECM) in vitro similar to corneal stromal tissue. METHODS Human corneal stromal stem cells (hCSSC) were isolated as side population cells by flow cytometry. Cloned hCSSC were cultured as free-floating pellets in serum-free media for 3 weeks. Gene expre...

Journal: :Nucleic acids research 1980
D Nelson J Covault R Chalkley

It has been previously shown that micrococcal nuclease digestion and subsequent fractionation of hen oviduct nuclei generates fractions enriched (first supernatant fraction - 1SF) and depleted (second supernatant fraction - 2SF) in ovalbumin genes, while a third fraction, the pellet fraction, contains about the same level of this gene as whole chromatin (Bloom and Anderson (1978) Cell 15, 141-1...

Journal: :Stem cell research 2013
Macarena Peran Sergio Ruiz Witek Kwiatkowski Juan Antonio Marchal Sheng-Lian Yang Antonia Aranega Senyon Choe Juan Carlos Izpisua Belmonte

Human adipose derived stem cells (hASCs) can be easily isolated and their plasticity has been well characterized. Several TGF-β superfamily ligands can direct hASCs towards chondrocytes. However, these ligands are difficult to purify and expensive. We have developed a library of Activin/BMP2 chimeric ligands (AB2 ligands) by systematically mixing their sequence segments and have tested their ch...

2014
Jing Chen Chenghai Li Sihong Wang

Osteoarthritis (OA) is one of diseases that seriously affect elderly people's quality of life. Human mesenchymal stem cells (hMSCs) offer a potential promise for the joint repair in OA patients. However, chondrogenic differentiation from hMSCs in vitro takes a long time (∼ 6 weeks) and differentiated cells are still not as functionally mature as primary isolated chondrocytes, though chemical st...

2003
BINGJUN HE WEI WEN SU

Mixing has been one of the important parameters in characterizing and designing external air-lift bioreactors for the biological processes that require intensive mixing for mass transfer. In this study, pH tracer method was employed to characterize the mixing quality of a three-phase laboratory-scale external-loop air-lift bioreactor (EALR) used for cultivation of a pelletized filamentous funga...

2017
Kyoung-Won Ko Bogyu Choi Sunghyun Park Yoshie Arai Won Chul Choi Joong-Myung Lee Hojae Bae In-Bo Han Soo-Hong Lee

Expansion of chondrocytes for repair of articular cartilage can lead to dedifferentiation, making it difficult to obtain a sufficient quantity of chondrocytes. Although previous studies have suggested that culture in a three-dimensional environment induces redifferentiation of dedifferentiated chondrocytes, its underlying mechanisms are still poorly understood in terms of metabolism compared wi...

2014
Gail Whiting Jun X Wheeler Sjoerd Rijpkema

The UK anthrax vaccine is an alum precipitate of a sterile filtrate of Bacillus anthracis Sterne culture (AVP). An increase in shelf life of AVP from 3 to 5 years prompted us to investigate the in vivo potency and the antigen content of 12 batches with a shelf life of 6.4 to 9.9 years and one bulk with a shelf life of 23.8 years. All batches, except for a 9.4-year-old batch, passed the potency ...

2017
Anika Witt Achim Salamon Diana Boy Doris Hansmann Andreas Büttner Andreas Wree Rainer Bader Anika Jonitz-Heincke

The main goal of cartilage repair is to create functional tissue by enhancing the in vitro conditions to more physiological in vivo conditions. Chondrogenic growth factors play an important role in influencing cartilage homeostasis. Insulin‑like growth factor (IGF)‑1 and transforming growth factor (TGF)‑β1 affect the expression of collagen type II (Col2) and glycosaminoglycans (GAGs) and, there...

Journal: :The Journal of Cell Biology 1968
Robert M. McCombs Matilda Benyesh-Melnick J. Pierre Brunschwig

A technique is described for embedding tissue culture cells that have been adsorbed or grown on Millipore filters. The acetone used during the embedding process rendered the filters transparent so that specific areas or cells could be chosen with the aid of the light microscope. Lymphoblastoid cells processed on the filters possessed well-defined plasma membranes and microvilli which were rarel...

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