Exo-spin midi columns Reference: EX04-5 Exo-spin™ technology combines precipitation and size exclusion chromatography (SEC), providing flexibility and performance. Using only precipitation for exosome isolation co-purifies large amounts of non-exosomal proteins and other material, as well as carried-over precipitant. SEC is reliable for exosome isolation, but a step is needed for low-exosome content starting material (such as cell culture media) to concentrate the sample prior to SEC isolation. For most applications, precipitation is the simplest way to achieve this concentration. Small samples can be purified directly. For larger samples we provide a simple, two-step protocol that allows consistent and reliable purification of samples in under 2 hours. Iterative loading can also be used to increase loading sample volume.
RPMI 1640, with L-Glutamine, powder medium, with 25 mM HEPES, w/o Sodium... Reference: RPMI-HA-P10 RPMI 1640 medium is widely suitable for supporting growth of many cell types. Compared to other media, it has a unique formulation comprising glutathione and high concentrations of vitamins.
DMEM Low Glucose (1 g/l), with Stable Glutamine, with Sodium Pyruvate Reference: DMEM-LPSTA Dulbecco's Modified Eagle Medium (DMEM) is a standard cell culture medium. It supports the growth of numerous cell types. The variety of available formulations suit many applications.
Internal Control DNA extra Reference: 11-1905 Additional internal amplification control for Venor®GeM Classic ('11-1905 )
Orangu™ Cell Counting Solution Reference: OR01-500 Non-cytotoxic: Further experiments can be carried out with the same cells Sensitive: wide linear range with low to high numbers of cells detected Easy to use: 15 minutes hands-on
Exo-spin midi columns Reference: EX04-20 Exo-spin™ technology combines precipitation and size exclusion chromatography (SEC), providing flexibility and performance. Using only precipitation for exosome isolation co-purifies large amounts of non-exosomal proteins and other material, as well as carried-over precipitant. SEC is reliable for exosome isolation, but a step is needed for low-exosome content starting material (such as cell culture media) to concentrate the sample prior to SEC isolation. For most applications, precipitation is the simplest way to achieve this concentration. Small samples can be purified directly. For larger samples we provide a simple, two-step protocol that allows consistent and reliable purification of samples in under 2 hours. Iterative loading can also be used to increase loading sample volume.
RPMI 1640, with L-Glutamine, powder medium, with 25 mM HEPES, w/o Sodium... Reference: RPMI-HA-P50 RPMI 1640 medium is widely suitable for supporting growth of many cell types. Compared to other media, it has a unique formulation comprising glutathione and high concentrations of vitamins.
DMEM Low Glucose (1 g/l), w/o L-Glutamine, with Sodium Pyruvate Reference: DMEM-LPXA Dulbecco's Modified Eagle Medium (DMEM) is a standard cell culture medium. It supports the growth of numerous cell types. The variety of available formulations suit many applications.
Internal Control DNA extra Reference: 11-9905 Additional internal amplification control for Venor®GeM qEP (11-9905)
Orangu™ Cell Counting Solution Reference: OR01-1000 Non-cytotoxic: Further experiments can be carried out with the same cells Sensitive: wide linear range with low to high numbers of cells detected Easy to use: 15 minutes hands-on
Exo-spin mini-HD columns Reference: EX05-5 Exo-spin™ technology combines precipitation and size exclusion chromatography (SEC), providing flexibility and performance. Using only precipitation for exosome isolation co-purifies large amounts of non-exosomal proteins and other material, as well as carried-over precipitant. SEC is reliable for exosome isolation, but a step is needed for low-exosome content starting material (such as cell culture media) to concentrate the sample prior to SEC isolation. For most applications, precipitation is the simplest way to achieve this concentration. Small samples can be purified directly. For larger samples we provide a simple, two-step protocol that allows consistent and reliable purification of samples in under 2 hours. Iterative loading can also be used to increase loading sample volume.