物料
TPE seal
composite regenerated cellulose (CRC)
polypropylene screen
stainless steel cap (for end; polypropylene-encapsulated)
质量水平
特点
holdup volume 170 mL (in feed channel)
制造商/商品名称
Pellicon®
参数
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
技术
analytical sample preparation: suitable
buffer exchange: suitable
protein purification: suitable (concentration)
高度
3.8 cm (1.51 in.)
长度
20.6 cm (8.1 in.)
宽度
17.8 cm (7 in.)
过滤面积
1.14 m2
膜面积
1.14 m2
重量萃取物
≤1500 mg/m2
基质
Ultracel® (Membrane)
孔径
30 kDa NMWCO
pH值(酸碱度)
2-13
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一般描述
The Pellicon® 3 Cassette with Ultracel® Membrane is designed for the filtration of therapeutic proteins (such as monoclonal antibodies) and recombinant and non-recombinant proteins.
This P3C030C10 Pellicon® 3 ultrafiltration device features a pore size of 30 kDa NMWCO, a filtration area of 1.14 m2, a PLCTK membrane, and dimensions measuring 2.4 cm (H) x 17.8 cm (W) x 20.6 cm (L).
特点和优势
- 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
其他说明
分析说明
法律信息
WGK
WGK 1
法规信息
商品
Find best practices for using Pellicon® Capsules in ADC processing as well as data from two studies using Pellicon® Capsules and Pellicon® cassettes in the ADC manufacturing process.
Get practical guidance on using single-pass tangential flow filtration in your downstream process and scaling between capsules and cassettes.
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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