Category: Cell Culture

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  • Categories: Exosome
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  • Categories: Primary cells
Reference: MOU-1B

Mouse Serum is obtained and pooled from normal mouse populations under strict conditions. It acts as a control or a blocking agent in binding assays.

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.

Reference: C-12225

Human Dermal Blood Endothelial Cells (HDBEC) adult donor

Reference: HAM-12-A

Ham's F-12 was developed for the cultivation of Chinese Hamster Ovary (CHO) cells. It is the medium of choice for supporting the growth of cells in serum-free conditions.

Reference: NCS-1A

Newborn Calf Serum (NBCS) is collected from 3 to 10 day old calves and can be used as a high-grade replacement for Fetal Bovine Serum.

Reference: EX05-20

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.

Reference: C-12226

Human Dermal Blood Endothelial Cells (HDBEC) adult donor

Reference: IMDM-A

Iscove's Modified Dulbecco's Medium (IMDM) is suitable for high density cultures. This modified DMEM formulation supports growth of different cell types such as Jurkat, COS-7 or macropahges.

Reference: NCS-1B

Newborn Calf Serum (NBCS) is collected from 3 to 10 day old calves and can be used as a high-grade replacement for Fetal Bovine Serum.

Reference: EX05-100

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.

Reference: C-12231

Human Saphenous Vein Endothelial Cells (HSaVEC)

Reference: L15-XA

Leibovitz's L-15 Medium was developed for carbon dioxide free systems. It is suitable for the cultivation of tumor and embryonic cells as well as HeLa and Hep-2.