BioParticles製品の使用について BioParticles™コンジュゲートは凍結乾燥粉末として提供されます。約3 x 108の大腸菌または黄色ブドウ球菌粒子/mg(固体)および約2 x 107のザイモサン粒子/mg(固体)が存在します。BioParticles™コンジュゲートは、食作用アッセイで使用するために選択した緩衝液で再構成できます。細胞の表面に結合している(しかし内部に取り込まれていない)BioParticles™コンジュゲートの蛍光は、エチジウムブロマイド、トリパンブルー、または他のクエンチャーよって消光できます。細胞での用途に加えて、蛍光BioParticles™コンジュゲートは、細菌や酵母変異体を分類する際のフローサイトメトリーキャリブレーションリファレンスとして有効な場合があります。微小粒子は、サイズと形状が特徴的に異なるため、光散乱研究の参考になる可能性もあります。
While the bacteria have been attenuated with formaldehyde and alcohol desiccation, the BioParticles products are not considered sterile, and we do not recommend incubation of more than 4 hours. This applies to all of our dye-labeled (pHrodo, Alexa Fluor, etc.) and unlabeled BioParticles products.
What is the type of bond that attaches the dyes to the BioParticles probes?
We use amine-reactive dyes to covalently attach fluorescent dyes to all of our BioParticles probes such as the Escherichia coli (K-12 strain) BioParticles probes, Staphylococcus aureus (Wood strain without protein A) BioParticles, and the Zymosan A (S. cerevisiae) BioParticles probes.
Phagocytosis and peroxidase release by seabream (Sparus aurata L.) leucocytes in response to yeast cells.
Authors:RodrÃguez A, Esteban MA, Meseguer J
Journal:Anat Rec A Discov Mol Cell Evol Biol
PubMed ID:12704699
A flow cytometric method was adapted to evaluate phagocytosis by gilthead seabream leucocytes after incubation with yeast cells (Saccharomyces cerevisiae). Head-kidney leucocytes were incubated in vitro for different times in different proportions with heat-killed fluorescein isothiocyanate (FITC)-labeled yeast cells to study the kinetics of phagocytosis. Attached and internalized yeast cells ... More
Conserved role of a complement-like protein in phagocytosis revealed by dsRNA knockout in cultured cells of the mosquito, Anopheles gambiae.
Authors:Levashina EA, Moita LF, Blandin S, Vriend G, Lagueux M, Kafatos FC
Journal:Cell
PubMed ID:11257225
'We characterize a novel hemocyte-specific acute phase glycoprotein from the malaria vector, Anopheles gambiae. It shows substantial structural and functional similarities, including the highly conserved thioester motif, to both a central component of mammalian complement system, factor C3, and to a pan-protease inhibitor, alpha2-macroglobulin. Most importantly, this protein serves as ... More
Simultaneous flow cytometric method to measure phagocytosis and oxidative products by neutrophils.
Authors:Perticarari S, Presani G, Mangiarotti MA, Banfi E
Journal:Cytometry
PubMed ID:1782835
'We developed a rapid and sensitive two-color flow cytometric method which allows the simultaneous quantification of both the phagocytosis rate and the oxidative burst activation of polymorphonuclear leukocytes (PMNLs). The oxidation of hydroethidine (HE) to ethidium bromide (EB) was performed by the oxidative neutrophil products within the cells during the ... More
Increase in phagocytosis after geldanamycin treatment or heat shock: role of heat shock proteins.
Authors:Vega VL, De Maio A
Journal:J Immunol
PubMed ID:16210633
'The response to injury is activated at the systemic and cellular levels. At the systemic level, phagocytosis plays a key role in controlling infections and clearing necrotic and apoptotic cells. The expression of heat shock proteins (Hsp), which is a well-conserved process, is a major component of cellular response to ... More
Quantitation of phagocytosis by confocal microscopy.
Authors:Babcock GF
Journal:Methods Enzymol
PubMed ID:10506981
'Confocal microscopy is an excellent tool to quantify phagocytosis. Depending on the particle used, phagocytosis can be determined by the simple manual counting of internalized particles. If a fluorescence probe is utilized, an analysis of fluorescence intensity can be used for quantification. The basic procedure can be altered in a ... More