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3M™ Zeta Plus™ BC Series Encapsulated Disposable Filter Capsule BC0025LVR06, 25 sq cm, EFA, Luer Lock, 4/Case

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3M™ Zeta Plus™ BC Series Encapsulated Disposable Filter Capsule BC0025LVR06, 25 sq cm, EFA, Luer Lock, 4/Case

About the product

3M™ Zeta Plus™ VR Series filter media is a family of cellulosic depth filtration media designed to retain contaminants by both physical entrapment and ion exchange absorption.

  • Overall Diameter (Imperial) : 2.63
  • Overall Diameter (Metric) : 66.8
  • End Modification : Luer
  • Filter Type : Depth
  • Grade : VR06
  • Application : Harvest and clarification
  • Filter Technology : Adsorbent
  • Industries : Biopharmaceutical manufacturing
  • Product Series : BC
  • Brand : Zeta Plus™

Product details

Zeta Plus VR Series Media are composed of high-area process filter aids embedded in a cellulose fiber depth matrix. During the manufacturing process, a cationic charge modifier is chemically bound to the matrix components, forming a permanent, interconnected, rigid depth filter with positively-charged electrokinetic capture sites. The resulting porous depth filter structure is a tortuous network of absorptive flow channels capable of retaining contaminating viruses through a combination of anion exchange absorption and mechanical entrapment. Cumulative viral titer reduction may also be attainable through a staged two-step Zeta Plus system.
  • Combined ion exchange & physical entrapment virus removal mechanisms
  • Viral log reduction
  • Economical purification product as adjunct or pre-fi lter to other viral clearance steps
  • Provides orthogonal method of viral clearance
  • Can replace or augment chromatography columns
  • Quality control tested for media ion exchange capacity provides assurance of filter media consistency and performance
  • FDA Drug Master File and USP Class VI Biological Safety that eases validation and regulatory submissions by providing vital documentation and traceability.
  • FDA Drug Master File and USP Class VI Biological Safety that eases validation and regulatory submissions by providing vital documentation and traceability.
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