Venor®GeM Classic Reference: 11-1050 Mycoplasma detection kit for conventional PCR without polymerase - EP 2.6.7/ JP, 17st edition, chapter G3 compliant
Exo-spin columns Reference: EX03-25 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, powder medium, with L-Glutamine, w/o Sodium Bicarbonate Reference: RPMI-A-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.
Goat Serum Reference: GOA-1B Goat Serum is obtained from normal healthy goats. It is broadly used as a blocking solution to reduce non-specific binding in antibody-based assays.
Fetal Bovine Serum Bioprocess, US Origin Reference: FBS-24A Fetal Bovine Serum (FBS) is the most frequently used growth supplement for cell culture media. FBS Bioprocess is tested according to 9CFR and EMEA.
Venor®GeM Classic Reference: 11-1100 Mycoplasma detection kit for conventional PCR without polymerase - EP 2.6.7/ JP, 17st edition, chapter G3 compliant
Exo-spin columns Reference: EX03-50 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, powder medium, with L-Glutamine, w/o Sodium Bicarbonate Reference: RPMI-A-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.
Horse Serum Reference: HOS-1A Horse Serum is an alternative to bovine serum for growth factors and hormones in cell culture studies. It is broadly used as a blocking agent in immunoassays.
Fetal Bovine Serum Bioprocess, US Origin Reference: FBS-24B Fetal Bovine Serum (FBS) is the most frequently used growth supplement for cell culture media. FBS Bioprocess is tested according to 9CFR and EMEA.
Venor®GeM Classic Reference: 11-1250 Mycoplasma detection kit for conventional PCR without polymerase - EP 2.6.7/ JP, 17st edition, chapter G3 compliant
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.