P3B030A01
Pellicon® 3 Cassette with Biomax® Membrane
30kDa, A Screen, 0.11 m2
Synonym(s):
Pellicon® 3 Cassette with Biomax 30 kDa Membrane, A screen, 0.11 m2
About This Item
Recommended Products
material
TPE seal
polyethersulfone
polypropylene cap (for end)
polypropylene screen
Quality Level
feature
holdup volume 9 mL (in feed channel)
manufacturer/tradename
Pellicon®
parameter
30 psi max. reverse press. exposure at 25 °C (for 24 hours)
4-6 L/min-m2 recirculation rate
40 psi max. transmembrane pressure at 4-50 °C
6.9 bar max. inlet pressure (100 psi)
80 psi max. transmembrane pressure at 4-40 °C
technique(s)
buffer exchange: suitable
protein purification: suitable (concentration)
H
2.16 cm (0.85 in.)
L
20.6 cm (8.1 in.)
W
5.6 cm (2.2 in.)
membrane area
0.11 m2
gravimetric extractables
≤1500 mg/m2
matrix
Biomax® (Membrane)
pore size
30 kDa NMWCO
pH
1-14
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General description
The Pellicon® 3 Cassette with Biomax® Membrane is perfect for the filtration of monoclonal antibodies and solutions containing albumin, hormones, vaccines and growth factors.
This P3B030A01 Pellicon® 3 ultrafiltration device features a pore size of 30 kDa NMWCO, a Biomax® 30 membrane, and dimensions measuring 2.16 cm (H) x 5.6 cm (W) x 20.6 cm (L).
Features and Benefits
- Rugged & reliable – ideally suited for today′s more demanding filtration processes
- High performance – produces excellent resolution, yields and back-pressure resistance
- Optimum product recovery – thanks to proven membrane technology
- Void-free technology – leading-edge membranes resolve virtually any separation challenge
- Defect-free, superior adhesion – Ultracel®uses composite membranes cast on a microporous substrate
- Automated manufacturing – delivers unbeatable performance, consistency and reliability
- Easy installation & care – simple to install and maintain
Other Notes
Analysis Note
Legal Information
Storage Class Code
8B - Non-combustible corrosive hazardous materials
WGK
WGK 1
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Certificates of Analysis (COA)
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Articles
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.
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.
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.
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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