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AABG01300

Millipore

MCE Membrane Filter, 0.8 μm Pore Size

MF-Millipore, filter diam. 13 mm, hydrophilic, black, gridded

Synonym(s):

MF-Millipore Membrane Filter, 0.8 µm pore size, gridded

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About This Item

UNSPSC Code:
40161507
eCl@ss:
32031602
NACRES:
NB.24

material

black filter
gridded
mixed cellulose esters (MCE) membrane

Quality Level

description

13 mm diameter, mixed cellulose esters (MCE) membrane, hydrophilic, black, gridded, 100 discs

sterility

non-sterile

feature

hydrophilic

manufacturer/tradename

MF-Millipore
Millipore

parameter

16 L/min-cm2 air flow rate
190 mL/min-cm2 water flow rate
75 °C max. temp.

filter diam.

13 mm

thickness

150 μm

gravimetric extractables

4%

color

black

matrix

MF-Millipore

pore size

0.8 μm pore size
82 % porosity

bubble point

≥1.0 bar, air with water at 23 °C

shipped in

ambient

General description

Biologically inert mixtures of cellulose acetate and cellulose nitrate have made MF-Millipore membrane filters one of the most widely used membranes in analytical and research applications.

MF-Millipore filters without Triton surfactant contain minimum amounts of wetting agent and have a lower water extractable content than standard MF-Millipore filters.

Features & Benefits:
- Versatile filter for biological and environmental monitoring applications
- Available in a range of pore sizes, colored black or white, with or without a gridded surface
- Compatible with ethylene oxide, gamma irradiation, and autoclave sterilization methods
Filter Code: AABG

Application

  • Fluorescent assays
  • Particle monitoring
  • Air monitoring
  • Microplastics

Legal Information

MF-Millipore is a trademark of Merck KGaA, Darmstadt, Germany

Signal Word

Danger

Hazard Statements

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2 - Flam. Sol. 1

WGK

WGK 3


Certificates of Analysis (COA)

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Craig S Pearson et al.
Experimental eye research, 190, 107859-107859 (2019-11-11)
The accumulation of chondroitin sulfate proteoglycans (CSPGs) in the glial scar following acute damage to the central nervous system (CNS) limits the regeneration of injured axons. Given the rich diversity of CSPG core proteins and patterns of GAG sulfation, identifying

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