نتایج جستجو برای: rhd – k562 cell line

تعداد نتایج: 1971298  

Journal: :iranian journal of blood and cancer 0
mehryar habibi roudkenar mahshid mohammadipour arezou oodi raheleh halabian naser amirizadeh nasser masrouri

background: the rh antigens are expressed as parts of a protein complex in the rbc membrane. this complex is a tetramer, consisting of two molecules of rhag and two molecules of rh proteins. to express rhd in rbc membrane, expression of rhag is essential. this co-expression only occurs in the erythroid lineage. k562 cell line has an erythroid lineage. materials and methods: cord blood was used ...

Amaneh Mohammadi Roshandeh, Arezou Oodi, Houri Rezvan, Kazem parivar, Mahshid Mohammadipour, Mehryar Habibi Roudkenar, Naser Amirizadeh, Nasser Masrouri, Raheleh Halabian,

Background: The Rh antigens are expressed as parts of a protein complex in the RBC membrane. This complex is a tetramer, consisting of two molecules of RhAG and two molecules of Rh proteins. To express RhD in RBC membrane, expression of RhAG is essential. This co-expression only occurs in the erythroid lineage. K562 cell line has an erythroid lineage. Materials and Methods: Cord blood was used ...

Journal: :Blood 2002
Isabelle Mouro-Chanteloup Anne Marie D'Ambrosio Pierre Gane Caroline Le Van Kim Virginie Raynal Didier Dhermy Jean-Pierre Cartron Yves Colin

In most cases, the lack of Rh in Rh(null) red cells is associated with RHAG gene mutations. We explored the role of RhAG in the surface expression of Rh. Nonerythroid HEK293 cells, which lack Rh and RhAG, or erythroid K562 cells, which endogenously express RhAG but not Rh, were transfected with RhD and/or RhAG cDNAs using cytomegalovirus (CMV) promoter-based expression vectors. In HEK293 cells,...

Journal: :iranian biomedical journal 0
علی زارعی محمودآبادی ali zaree mahmodabady حمید رضا جوادی hamid reza javadi مهدی کمالی mehdi kamali علی نجفی ali najafi زهرا حجتی zahra hojati

background: rna interference (rnai) is the mechanism of gene silencing-mediated messenger rna degradation by small interference rna (sirna), which becomes a powerful tool for in vivo research, especially in the areas of cancer. in this research, the potential use of an expression vector as a specific sirna producing tool for silencing of bcr-abl in k562 cell line has been investigated. methods:...

Journal: :Blood 1998
R Beckmann J S Smythe D J Anstee M J Tanner

Human K562 erythroleukemia cells were transfected with human band 3 (anion exchanger 1 [AE1]) cDNA, using the pBabe retroviral vector. Stable K562 clones expressing band 3 were isolated by flow cytometry, and surface expression was quantified by immunoblotting. The function of band 3 expressed at the cell surface was demonstrated in chloride transport assays. K562 cells expressing band 3 also d...

1999
Kimita Suyama Hua Li Alex Zhu

In the Rh blood system, RhAG (Rhassociated glycoprotein, or Rh50) is thought to be involved in Rh30 (D, CE) expression by forming a protein complex on the red cell surface. To obtain further insight into the Rh complex, we chose nonerythroid COS-1 cells instead of proerythroblast-like K562 cells, which produce endogenous Rh proteins as cell host, for the expression of both RhAG and RhD. The RhA...

Journal: :Blood 2000
K Suyama H Li A Zhu

In the Rh blood system, RhAG (Rh-associated glycoprotein, or Rh50) is thought to be involved in Rh30 (D, CE) expression by forming a protein complex on the red cell surface. To obtain further insight into the Rh complex, we chose nonerythroid COS-1 cells instead of proerythroblast-like K562 cells, which produce endogenous Rh proteins as cell host, for the expression of both RhAG and RhD. The Rh...

Journal: :cell journal 0
karim shams mahshid saleh aliakbar movassaghpour parvin akbarzadeh zahra molaeipour

objective: bone marrow mesenchymal stem cells reside in bone marrow and support homing and differentiation of hematopoietic stem cells (1). this makes them an excellent instrument for regenerative treatment and co-culture with the hsc. materials and methods: in this study, k562 cell lines were treated with butyric acid(for erythroid differentiation), co-cultured with mesenchymal stem cells and ...

Journal: :iranian red crescent medical journal 0
farzaneh bonyadi department of comparative histology, faculty of veterinary medicine, urmia university, urmia, ir iran vahid nejati department of biology, faculty of science, urmia university, urmia, iriran amir tukmechi department of pathobiology and biotechnology, artemia and aquatic animals research institute, urmia university, urmia, ir iran shapour hasanzadeh department of comparative histology, faculty of veterinary medicine, urmia university, urmia, ir iran; department of comparative histology, faculty of veterinary medicine, urmia university, urmia, ir iran. tel: +98-09144475731 aram mokarizadeh cellular and molecular research center, kurdistan university of medical sciences, sanandaj, ir iran

methods s. cerevisiae was cultured and then disrupted by sonication. after centrifugation, the harvested supernatant was considered to be a cytoplasmic extract. the protein concentration was determined by the biuret method and the extract was diluted to concentrations of 500, 1000, and 2000 µg protein/ml. the frequencies of apoptosis and necrosis were assessed in extract-treated k562 cells by e...

توکمه‌چی, امیر, مکریانی, سالار, نوجوان, مجید,

Background: Chronic myeloid leukemia is a common cancer in human, so the goal of this study was the use of natural compound such as cell wall obtained from Saccharomyces cerevisiae (S. cerevisiae) and Saccharomyces boulardi (S. boulardi) and zinc nanoparticles on the growth inhibition of K562 cell line. Methods: For cell wall preparation, both yeasts were cultured in a basic medium at a...

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