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Key Documents

PCC300C15C

Millipore

Pellicon® Capsule with Ultracel® Membrane

C Screen, 1.5 m2 AseptiQuik® G connectors

Synonym(s):

Pellicon® Capsule with Ultracel® Membrane

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About This Item

UNSPSC Code:
23151806

material

EPDM rubber seal
PPO/PS blend (core)
PPO/PS blend housing
TPE seal
composite regenerated cellulose (CRC) membrane
epoxy adhesive
polyester screen
polypropylene screen
polyurethane adhesive

Quality Level

sterility

sterile; γ-irradiated

product line

Pellicon®

feature

holdup volume 456 mL (in feed channel)
holdup volume 741 mL (in permeate channel)

packaging

package of 1

parameter

max. inlet pressure at 75 psi (5.1 bar) and 4-30 °C
max. transmembrane pressure at 45 psi (3.1 bar) and 4-30 °C
4-6 L/min-m2 flow rate

technique(s)

ultrafiltration: suitable

diam.

10.3 cm (4.1 in.)

filtration area

1.5 m2

screen size

, Type C screen (coarse screen)

size

43.7 cm (17.2 in.) , Length

impurities

≤5 ppm Meets TOC (in retentate effluent, after a WFI flush of 20 L/m²)

matrix

Ultracel®

pore size

300 kDa

pH range

2-13

storage temp.

15-25°C

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General description

The Pellicon® Capsule is the first of its kind -- a true single-use TFF device that comes ready to process in minutes. Self-contained, it employs an easy-to-use, holderless format and is supplied sterilized by irradiation.
Feed: AseptiQuik® G Connector
Permeate: AseptiQuik® G Connector
Retentate: AseptiQuik® G Connector
Permeate: AseptiQuik® G Connector

Application

Viral Gene Therapies, Vaccines, Concentration, Diafiltration, Buffer exchange, Protein purification, mRNA

Features and Benefits

  • Plug ′n play, holderless design - easy to install, safe to remove
  • Gamma Sterilized and preseravtive-free - ready to process in minutes
  • True single-use, self-contained capusle - fast, safe, and flexible batch turnaround
  • Proven Ultracel® membrane and C screen - high recovery, superior mass transfer, solvent resistance
  • Pellicon® TFF proven performance - true linear scalability within Pellicon® TFF families

Packaging

A foam clamshell is inserted over the end caps on both ends of the capsule which is then double-bagged and vacuum sealed. The double-bagged capsule is placed on a tray and then individually boxed.

Other Notes

The Emprove® Program complements the product portfolio through

  • Comprehensive documentation to support qualification, risk assessment and process optimization needs.
  • Consolidation of product specific testing, quality and regulatory information to simplify compliance requirements.
  • Convenient 24/7 access to up-to-date product information.

Legal Information

AseptiQuik is a registered trademark of Colder Products Company
Emprove is a registered trademark of Merck KGaA, Darmstadt, Germany
Pellicon is a registered trademark of Merck KGaA, Darmstadt, Germany
ULTRACEL is a registered trademark of Merck KGaA, Darmstadt, Germany

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Articles

Our overview of scalable tangential flow filtration for viral vector production will provide key considerations for developing and optimizing your downstream process.

Our overview of scalable tangential flow filtration for viral vector production will provide key considerations for developing and optimizing your downstream process.

Our overview of scalable tangential flow filtration for viral vector production will provide key considerations for developing and optimizing your downstream process.

Our overview of scalable tangential flow filtration for viral vector production will provide key considerations for developing and optimizing your downstream process.

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