Lipids & Polymers

TrueBlot® Magnetic Beads are uniform, non-aggregating, super-paramagnetic beads consisting of a ferric oxide core functionalized with various silane groups. The super-paramagnetic nanoparticles are coupled with a biomolecule, such as Protein G, and are specifically designed, tested and quality controlled for isolation and purification of antibodies, and immunoprecipitation methods using manual or automatic platforms. Protein G, attached to magnetic bead surface, can bind to antibodies from many different species, including mouse, human, rabbit, cow, goat and sheep. Immunoprecipitation assays with Protein G magnetic beads result in high capture efficiencies and high yield of target antigen. Protein G magnetic beads are stable, pre-blocked beads that provide highly purified product. Bead mean diameter is ~0.5 μm, bead concentration is 5.0 mg/mL, and binding capacity is ≥ 80 μg rabbit IgG/mg of beads.

TrueBlot® Magnetic Beads are uniform, non-aggregating, super-paramagnetic beads consisting of a ferric oxide core functionalized with various silane groups. The super-paramagnetic nanoparticles are coupled with a biomolecule, such as Streptavidin, and are specifically designed, tested and quality controlled for magnetic purification of biotin-labeled components using manual or automatic platforms. Streptavidin magnetic beads are stable, pre-blocked beads with high binding capacity that provide rapid and efficient biomolecule purification from complex samples. Bead mean diameter is ~0.5 μm, bead concentration is 5.0 mg/mL, and binding capacity is ≥ 60 µg biotin/mg of beads.

TrueBlot® Magnetic Beads are uniform, non-aggregating, super-paramagnetic beads consisting of a ferric oxide core functionalized with various silane groups. The super-paramagnetic nanoparticles are coupled with a biomolecule, such as Streptavidin, and are specifically designed, tested and quality controlled for magnetic purification of biotin-labeled components using manual or automatic platforms. Streptavidin magnetic beads are stable, pre-blocked beads with high binding capacity that provide rapid and efficient biomolecule purification from complex samples. Bead mean diameter is ~0.5 μm, bead concentration is 5.0 mg/mL, and binding capacity is ≥ 60 µg biotin/mg of beads.

This product contains Concanavalin A (ConA) conjugated to paramagnetic microspheres. ConA is a lectin (carbohydrate-binding protein) that binds specifically to mannosyl- and glucosyl-containing extracellular glycoproteins. The ConA magnetic beads are therefore useful to immobilize cells or nuclei presenting these glycans in their extracellular matrices.

1 2-Dioleoyl-sn-glycero-3-phosphoethanol (DOPEth) is a form of phosphatidylethanol (PEth) which is formed primarily by transphosphatidylation of phosphatidylcholine (PC) by phospholipase D. Most PEth (about 75%) is incorporated into erythrocyte membranes and is one of the longest-lived circulating EtOH metabolite yet identified. DOPEth is a one of five most abundant naturally occurring PEth species.

1-Palmitoyl-2-oleoyl-sn-glycero-3-phosphoethanol (POPEth) is a form of phosphatidylethanol (PEth) which is formed primarily by transphosphatidylation of phosphatidylcholine (PC) by phospholipase D. Most PEth (about 75%) is incorporated into erythrocyte membranes and is one of the longest-lived circulating EtOH metabolite yet identified. POPEth is a one of five most abundant naturally occurring PEth species.

1-Palmitoyl-2-linoleoyl-sn-glycero-3-phosphoethanol (PLPEth) is a form of phosphatidylethanol (PEth) which is formed primarily by transphosphatidylation of phosphatidylcholine (PC) by phospholipase D. Most PEth (about 75%) is incorporated into erythrocyte membranes and is one of the longest-lived circulating EtOH metabolite yet identified. PLPEth is a one of five most abundant naturally occurring PEth species.

1-Stearoyl-2-linoleoyl-sn-glycero-3-phosphoethanol (SLPEth) is a form of phosphatidylethanol (PEth) which is formed primarily by transphosphatidylation of phosphatidylcholine (PC) by phosphlipase D. Most PEth (about 75%) is incorporated into erythrocyte membranes and is one of the longest-lived circulating EtOH metabolite yet identified. SLPEth is a one of five most abundant naturally ocurring PEth species.

The Pure Liposome is prepared form asolectin through homogenizing the asolectin suspension with an ultrasonic homogenizer. And it is raw material for proteoliposome proteins production by <i>in vitro<i> wheat germ expression system.