Category: Cell Culture

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  • Categories: Exosome 
  • Categories: Mycoplasma
  • Categories: Other Serum
  • Categories: Primary cells
  • Categories: Transfection
Reference: EX01-8

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: ciPTEC14.4

CiPTEC 14.4 is a human conditionally immortalized proximal tubular epithelial cell line. Stably transfected by SV40T and hTERT, subcloned and well-characterized. Expressing proximal tubular markers alkaline phosphatase, di-peptidiyl peptidase IV and ZO-1.

Reference: BLA-1X

Blasticidin S is used as a selection antibiotic that inhibits protein synthesis in bacteria and eukaryotes. Transformed cells containing the resistance genes bls, bsr, or BSD can be selected.

Reference: ABS-1A

Adult Bovine Serum (ABS), collected from adult cattle, is used to supplement cell culture media. It is highly suitable for in vitro cultivation of multiple cell types.

Reference: EX01-25

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.

Reference: cipTECOAT1

Based on ciPTEC 14.4, including expression and functional uptake via organic anion transporter 1 (SLC22A6)

Reference: BLA-5X

Blasticidin S is used as a selection antibiotic that inhibits protein synthesis in bacteria and eukaryotes. Transformed cells containing the resistance genes bls, bsr, or BSD can be selected.

Reference: ABS-1B

Adult Bovine Serum (ABS), collected from adult cattle, is used to supplement cell culture media. It is highly suitable for in vitro cultivation of multiple cell types.

Reference: EX01-25L

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: cipTECOAT3

Based on ciPTEC 14.4, including expression and functional uptake via organic anion transporter 3 (SLC22A8)

Reference: ABS-1D

Adult Bovine Serum (ABS), collected from adult cattle, is used to supplement cell culture media. It is highly suitable for in vitro cultivation of multiple cell types.