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安全信息

HCDC0001L102

Millipore

Mobius Gold High Cell Density Cryopreservation Assembly

(-80C), 250 mL, sterile; γ-irradiated (at 25-40 kGy)

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别名:
Mobius® Gold High Cell Density Cryopreservation Assembly (-80C), 250 mL
UNSPSC代码:
41103801

物料

device (thermoplastic elastomer)
polyethylene device
polypropylene device
silicone device

质量水平

400

Agency

according to ISO 11137
meets EN 2.6.14
meets JP 4.01
meets USP 85

无菌性

sterile; γ-irradiated (at 25-40 kGy)

产品线

Mobius®

参数

-80-60 °C temp. range (-112-140 °F)
0.3 bar max. pressure (4.4 psi)
150 mL process volume

容量

250 mL

杂质

<0.25 EU/mL Aqueous extraction (LAL test)

应用

mAb

储存温度

2-30°C

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一般描述

Device configuration: 5 bags per assembly
Device configuration: 5 bags per assembly
Our Mobius® High Cell Density Cryopreservation (HCDC) Assembly (-196C) is a single-use assembly specially designed to facilitate the freeze and thaw of cryopreserved cells in liquid nitrogen vapor phase (? -196°C). Available in two assembly bag sizes of 100 mL and 250 mL, our Mobius® HCDC Assembly (-196C) enables seed train inoculation with cells at a higher cell density and larger volume compared to the traditional seed train process using vials, which significantly accelerates the cell expansion process. Our Mobius® single-use assembly also provides a closed processing environment preventing contamination while improving process reproducibility.
Our Mobius® High Cell Density Cryopreservation (HCDC) Assembly (-80°C) is a single-use assembly specially designed to facilitate the freeze and thaw of cryopreserved cells at -80°C. Available in two assembly bag sizes of 100 mL and 250 mL, our Mobius® HCDC Assembly (-80°C) enables seed train inoculation with cells at a higher cell density and larger volume compared to the traditional seed train process using vials, which significantly accelerates the cell expansion process. Our Mobius® single-use assembly also provides a closed processing environment preventing contamination while improving process reproducibility.

特异性

All component materials, in contact with sampling liquid, meet the criteria for Class VI testing based on USP <88> Biological Reactivity, in vivo.
All component materials, in contact with sampling liquid, meet the criteria for Class VI testing based on USP <88> Biological Reactivity, in vivo.
Application

应用

Croyopreserved storage of cells

包装

Five (5) assembies per package with each assembly containing five (5) 100 mL cryo bags
Five (5) assembies per package with each assembly containing five (5) 250 mL cryo bags

组分

Fluoropolymer bags: Tubing: Silicone and Thermoplastic ElastomerFittings: PolypropyleneNovaSeal Pinch Pipes: Nickel plated brass
Pinch clamp: Nylon
Polyethylene bags: Pureflex FilmTubing: Silicone and Thermoplastic ElastomerFittings: PolypropyleneNovaSeal Pinch Pipes: Nickel plated brassPinch clamp: Nylon

其他说明

Bags manufactured under ISO Clean Room Class 8 conditions in a facility certified to ISO 14644-1 standards. Assembly performed under ISO Clean Room Class 7 conditions in a facility certified to ISO 14644-1 standards.
Bags manufactured under ISO Clean Room Class 8 conditions in a facility certified to ISO 14644-1 standards. Assembly performed under ISO Clean Room Class 7 conditions in a facility certified to ISO 14644-1 standards.

法律信息

MOBIUS is a registered trademark of Merck KGaA, Darmstadt, Germany

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Impact of DMSO And Freezing Technique in Developing a High Cell Density Cryopreservation Process for Upstream Bioprocessing

Understand how considerations such as DMSO concentrations and freezing techniques are key in the successful implementation of high cell density cryopreservation (HCDC).

Seed Train Intensification Using High Cell Density Cryopreservation

High cell density cryopreservation (HCDC) is a closed processing alternative to the traditional seed train expansion process. Learn more about the benefits of HCDC.

Reducing the Need for Animal Testing for Biological Reactivity in Polymer Characterization

This page provides an overview of USP <87>, <88>, and <1031>, compares bioreactivity testing, and describes the transition of our organization towards in vitro test methods.

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