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Cell Freezing and Preservation Media

Store Your Cells and Tissues with Optimized Cryopreservation Media

Storage and cryopreservation of cells and tissues are vital parts of the workflow for biological research. Your choice of freezing medium can influence the quality of your banked cells and future experiments. Ensure high cell viability and functional stability following storage and thawing by using a reliable cryopreservation medium offered 海角破解版.

Choose from cGMP-manufactured, protein- and/or serum-free freezing and biopreservation media to preserve your cells and tissues. For long-term storage of your cells in low temperature environments (-80掳C to -196掳C), opt for a ready-to-use freezing medium such as CryoStor庐 CS10 or 尘贵谤别厂搁鈩. For short-term hypothermic preservation (2 鈥 8掳C), you can use a preservation medium such as HypoThermosol庐 FRS. Explore all our cell freezing and preservation media to meet your cryopreservation workflow needs for different cell types.

Image showing a liquid nitrogen tank used to cryopreserve cells and tissues

Cryopreservation Basics: Protocols and Best Practices for Freezing Cells

Learn the fundamentals of cell cryopreservation and find best practices for freezing down your cells in this resource.

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cGMP-Manufactured Cell Freezing and Preservation Media

CryoStor庐 Freezing Media

Cell and Tissue Types:

  • Immune cells, hepatocytes, human peripheral blood mononuclear cells (PBMCs), Chinese Hamster Ovary (CHO) cells, myeloma cell lines, hybridomas, human mesenchymal stromal cells (MSCs), human embryonic and induced pluripotent stem cells (ES and iPS cells), mouse organoids, and other extremely sensitive cell and tissue types.

Recommended For:

  • Long-term storage of cells and tissues at low-temperature environments (-80掳C to -196掳C)

Features:

  • Designed to mitigate temperature-induced molecular stress responses during freezing and thawing

Formulation:

  • CryoStor庐 CS2, CryoStor庐 CS5, and CryoStor庐 CS10 are pre-formulated with 2%, 5%, and 10% USP-grade DMSO, respectively.
  • CryoStor庐 CSB is the DMSO-free base formulation of CryoStor庐 products that can be used in your workflow to reduce the level of cryopreservation-induced delayed-onset cell death.
  • cGMP-manufactured

BloodStor庐 Freezing Media

Cell Types:

  • Cord blood and tissue, peripheral blood and bone marrow

Recommended For:

  • Cryopreservation of stem cells and other cells isolated from umbilical cord blood, peripheral blood, bone marrow, and other biologics

Features:

  • Formulated to be compatible with many automated stem cell banking systems

Formulation:

  • BloodStor庐 55-5 is preformulated with 55% (w/v) DMSO USP, 5% (w/v) Dextran-40 USP, and water-for-injection (WFI)-quality water
  • BloodStor庐 100 contains 100% (w/v) DMSO USP
  • cGMP-manufactured

HypoThermosol庐 FRS Preservation Media

Cell Types:

  • All cells and tissues including pluripotent stem cells, hematopoietic stem and progenitor cells, and mesenchymal stromal cells

Recommended For:

  • Short-term storage and/or shipment of cells at 2 鈥 8掳C rather than at cryogenic temperatures

Features:

  • Uniquely formulated to address the molecular-biological response of cells during the hypothermic preservation process

Formulation:

  • HypoThermosol庐 FRS preservation media is a serum-, protein-, and animal component-free medium
  • cGMP-manufactured
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Why Use cGMP-Manufactured Freezing Media?

Smooth your path through the regulatory landscape with cGMP-manufactured freezing and preservation media formulated using USP-grade ingredients. By using cGMP-manufactured freezing media, you can ensure that the products are consistently produced and controlled according to quality standards; an important consideration when you plan to move to the clinic in the future.


Defined and Serum-Free Cryopreservation Media

尘贵谤别厂搁鈩 and FreSR-S鈩 Cryopreservation Media

Cell Types:

  • Human embryonic stem (ES) and induced pluripotent stem (iPS) cells

Recommended For:

  • Cryopreservation of ES and iPS cells cultured in TeSR鈩 media

Features:

  • Higher thawing efficiencies than with conventional methods using serum1-4
  • 贵谤别厂搁鈩-厂 is optimized for cryopreservation of cells in single cell suspension

Formulation:

  • 贵谤别厂搁鈩-厂 is an animal component-free (ACF) medium, optimized for cryopreservation of cells in single cell suspension

MesenCult鈩-ACF Cryopreservation Medium

Cell Types:

  • Mesenchymal stem cells (MSCs)

Recommended For:

  • Cryopreservation of MSCs, including human MSCs previously cultured in MesenCult鈩-XF or MesenCult鈩-ACF media

Features:

  • Thawed MSCs have reproducibly high recovery rates and maintain MSC multipotency and expansion capacities

Formulation:

  • MesenCult鈩-ACF Freezing Medium is a defined, serum-free and animal component-free medium that contains DMSO

STEMdiff鈩 Neural Progenitor Freezing Medium

Cell Types:

  • Neural progenitor cells (NPCs) derived from human pluripotent stem cells

Recommended For:

  • Cryopreservation of NPCs generated from ES or iPS cells using STEMdiff鈩 Neural Induction Medium

Features:

  • NPCs can be frozen at any point post-neural induction with reproducibly high recovery rates
  • Post-thaw, NPCs display healthy morphology, express NPC markers and retain the potential to expand and differentiate into neurons, astrocytes and other neural cell types

Formulation:

  • STEMdiff鈩 Neural Progenitor Freezing Medium as a defined and serum-free medium containing DMSO
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Why Use Serum-Free Cryopreservation Media?

Lab-made formulations of freezing medium often contain fetal bovine serum (FBS). However, FBS contains undefined components, such as growth factors and hormones, and its use in freezing media raises concerns about lot-to-lot variability and the risk of transmitting potentially infectious agents. FBS is usually not recommended for cell banking, commercial, or clinical applications, such as the production of biologicals.

Data

Immune Cells Cryopreserved in 颁谤测辞厂迟辞谤庐颁厂10 Show Reproducibly High Post-Thaw Cell Viability

Figure 1. Immune Cells Cryopreserved in 颁谤测辞厂迟辞谤庐颁厂10 Show Reproducibly High Post-Thaw Cell Viability

颁谤测辞厂迟辞谤庐颁厂10 effectively mitigates temperature-induced molecular cell stress responses to maximize post-thaw viability and recovery for a variety of immune cell types, including T cells (data not shown) and B cells. Here, human B cells from 6 different donors cryopreserved in 颁谤测辞厂迟辞谤庐颁厂10 show reproducibly high viability after thawing, as measured by Propidium Iodide staining (ranging from 94.3 - 97.9%).

Immune Cells Cryopreserved in 颁谤测辞厂迟辞谤庐颁厂10 Retain Functionality Post-Thaw

Figure 2. Immune Cells Cryopreserved in 颁谤测辞厂迟辞谤庐颁厂10 Retain Functionality Post-Thaw

(A) Human peripheral blood Pan-T cells cryopreserved in 颁谤测辞厂迟辞谤庐颁厂10 were thawed and cultured with or without the addition of T cell activating factors. Cells from Donors 1-3 were cultured in RPMI Medium supplemented with 10% FBS, with (activated) or without (control) 40 ng/mL PMA and 1 ug/mL Ionomycin for 24 hours. Cells from Donors 4-5 were cultured in ImmunoCult鈩-XF T Cell Expansion Medium (Catalog #10981), with (activated) or without (control) ImmunoCult鈩 Human CD3/CD28 T Cell Activator (Catalog #10971) for 48 hours. Supernatants were collected from the cultures, and concentrations of secreted cytokines were determined using the Human IL-2 ELISA Kit (Catalog #02006). Activation by either PMA and Ionomycin or ImmunoCult鈩 Human CD3/CD28 T Cell Activator led to increased secretion of IL-2 compared to unstimulated control cultures. (B) Human B cells (Donors 6 - 11) cryopreserved in 颁谤测辞厂迟辞谤庐颁厂10 were thawed and activated with 1 碌g/mL CD40 and 100 ng/mL IL-21 for 7 days. Supernatants were collected from the cultures and immunoglobulin G (IgG) production was measured using the Human IgG ELISA Antibody Pair Kit (Catalog #01994). Compared to unstimulated control cultures, B cell activation led to increased IgG鈥 鈥媠ecretion.

尘贵谤别厂搁鈩 Improves Thawing Efficiencies 5- to 10-Fold over Other Reported Methods

Figure 3. 尘贵谤别厂搁鈩 Improves Thawing Efficiencies 5- to 10-Fold over Other Reported Methods

H9 hESCs were cryopreserved in 尘贵谤别厂搁鈩 at the indicated passage number. Thawing efficiencies were analyzed by counting the number of surviving clumps after thawing.


Related Products to Complete Your Freezing & Thawing Workflow

Complete your cryopreservation workflow by preserving your cells and tissues in sterile, self-standing cryogenic vials of different sizes and cap colors. Or obtain consistent freezing profiles using an alcohol-free container ideal for the cryopreservation of most cells and cell lines. Explore products for sterile cryostorage and freezing below:

Product Name
Catalog #
Corning庐 Cryogenic Vials with Orange Caps
Corning庐 Cryogenic Vial Cap Inserts
Corning庐 CoolCell庐 LX Cell Freezing Container

For downstream processing, researchers can thaw their cryopreserved cells using the ThawSTAR庐 CFT2 Automated Thawing System鈥攁 water-free instrument that delivers cell thawing profiles similar to those of a water bath. Conveniently thaw your cells in the biosafety cabinet, in ~2.5 minutes, while you prepare for the next step in your experiment.


Standardize Your Cell Thawing Process

Increase confidence in your cell thawing workflow by ensuring sample sterility and consistent thawing performance with ThawSTAR庐 CFT2鈥攁 sensor-based automated thawing system.

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Cell Thawing Demonstration

Step-by-Step Cell Thawing Demonstration

Follow this step-by-step protocol video to see how ThawSTAR庐 CFT2 could fit in your laboratory鈥檚 cell thawing workflow.

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Protocols and Technical Tips for Freezing and Thawing Cells


References

  1. Fujioka T, et al. (2004) Int J Dev Biol 48(10): 1149-54
  2. Ha SY, et al. (2005) Hum Reprod 20(7): 1779-85
  3. Ji L, et al. (2004) Biotechnol Bioeng 88(3): 299-312
  4. Ware CB, et al. (2005) Biotechniques 38(6): 879-80, 882-3