CryoScarless DMSO-Free (Trial) (Only 1 Per Customer)

Product#: FNK-CPL-A1-Trial
$1.05
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CryoScarless DMSO-Free (*Only 1 Per Customer*)

Cat. No. FNK-CPL-A1-Trial
Size 100 ml
Storage 4°C
NIH NSN# 655000L129025
Note 
Containing no DMSO and proteins

Product ID and Size
 

Cat No. Size Link
FNK-CPL-A1 100ml Mammalian Cell Culture, Animal Cell Culture-Classic Media, Diagnocine
FNK-CPL-A1-Trial Trial Mammalian Cell Culture, Animal Cell Culture-Classic Media, Diagnocine



Description

Let’s preserve your cells in a “no DMSO and Serum" condition!
CPL-A1_fig3.jpg     VPL-A1_2.jpg 
[ For cryopreservation of Stem Cells = the "StemCell Keep" ]

Protocol
 
Cultured cells in a liquid suspension form can be cryo-preserved with minimal damages from freezing and thawing steps. CryoScarless DMSO-Free preserves them with high viability and physiological activity. CryoScarless DMSO-Free includes no DMSO and no animal proteins.
 
Usage
1. Freezing cell suspensions
  1. Centrifuge suspended media of cultured cells and pellet them by elimination of supernatant at 4 ~ 10 °C.
  2. Resuspend the cell pellet with CryoScarless DMSO-Free at a preferred concentration of 5 × 105 ~ 5 × 106 cell/mL.
  3. Pipette the cell suspension into a cryotube at 1mL/vial and freeze them at –80 °C.
  4. For longer preservation, transfer the cryotube into a liquid nitrogen chamber (-196 °C) on the following day
2. Restoring live tissues from preserved state
  1. Warm the cryotube containing the preserved cells in a water bath at 37 °C by gently shaking the tube and thaw the contents.
  2. Centrifuge the cells and wash in cold PBS before transferring the cells to an experimental medium. When the live cells are used for experiments or cultured, place them under proper physiological conditions as soon as possible (e.g. 37 °C).
Expiration
CryoScarless DMSO-Free can be used for 2 years after the manufacture date if stored properly at 4 °C or –20 °C
 
Storage
Left-over solution can be stored at 4 °C or –20 °C for 2 years without loosing its functional quality.

Quality Control:
Bacterial tests:
Bacteria, fungi or mycoplasma
contamination is all negative.

Chemical tests:
(1) pH = 6.7 ~ 8.0 at RT
(2) Endotoxin < 0.5 EU/mL
Memo
Existent problem of preservation media contains DMSO and What is vitrification?

Very old method of cryopreservation was “Slow Programmed Freezing” using by 10% DMSO contained solution. However, big ice crystal is formed by this method and this crystal causes very poor cell viability (0.1-1%) for primate ES and iPS cells. Improved method is “vitrification” using by DAP213 (DMSO 2M, Acetamide 1M, Propylene glycol 3M).

Vitrification is the new method for preventing ice crystal formation by rapid freezing (<15 sec) in LN2. However, this method requires rapid thawing to prevent recrystallization and experienced operators. It is known that DMSO has influence on OCT-4 expression and differentiation, Acetamide is identified as carcinogens. Moreover, DAP213 is high osmolarity solution – it means this solution has high toxicity. Therefore, development of low Toxicity, easy to use vitrification solution had been expected.StemCell Keep is the solution that overcomes these disadvantages of DAP213!

VPL-A1_3.jpg

Solution freezed by Liquid Nitrogen is heated by 50℃/min.
StemCell Keep does not have recrystallization during temperature rising.

Features

  • Animal-derived Protein-free, Serum-free and DMSO-free formulation. No risk of differentiation effect by DMSO.
  • Xeno-freee.
  • Maintain ES and iPS cells with colony formation by vitrification.
  • Maintain stem cell pluripotency after thawing.
  • High cytoprotection effect and vitrification technology by new original cryoprotectant material is allowed to cryopreserve ES and iPS cell colonies.
  • Sufficient for 100 vials.
  • Free of bacteria, fungi and mycoplasma contamination.
  • Long shelf life. The product is stable for 2 years at 4C after the date of manufacture.
  • Free Trial Sample is available! (Please contact us) 
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Comparison Data
VPL-A1_4.jpg 

Outline Video
 

Handling Video
 
 
 
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