Venor®GeM Classic Reference: 11-1050 Mycoplasma detection kit for conventional PCR without polymerase - EP 2.6.7/ JP, 17st edition, chapter G3 compliant
Phytohemagglutinin M (PHA-M) for Lymphocyte Stimulation Reference: PHA-H Phytohemagglutinin M (PHA-M) for Lymphocyte Stimulation is a mitogen used for the stimulation of cell proliferation in lymphocyte cell cultures. It also has a powerful erythroagglutinating property.
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.
Dulbecco’s PBS (1x), powder, w/o Ca & Mg, w/o Phenol Red Reference: PBS-1A-P50 Dulbecco's phosphate-buffered saline (DPBS) is a buffer used in numerous biological applications. It maintains the milieu in a viable physiological range to sustain cells.
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.
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 Buffer Reference: EX06-30 Exo-spin™ products provide a proven, rapid and reliable way of generating high-quality purified exosomes suitable for a range of research applications.
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.
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 Buffer Reference: EX06-250 Exo-spin™ products provide a proven, rapid and reliable way of generating high-quality purified exosomes suitable for a range of research applications.
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.