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MCR40027H1

Millipore

Millistak+® Pod Depth Filter

CR40, cellulose (with active carbon), filtration area 0.027 m², Lab Scale

Synonym(s):

Millistak+ Pod Depth Filter, CR40 media series, 0.027 m2 surface area, 1/pack

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About This Item

UNSPSC Code:
23151806
eCl@ss:
32031690
NACRES:
NB.24
Pricing and availability is not currently available.

Product Name

Millistak+® Pod Depth Filter, CR40, cellulose (with active carbon), filtration area 0.027 m2, hydrophilic

material

cellulose (with active carbon)
polypropylene

Quality Level

400

description

Activated carbon is a very versatile process aid and has a high affinity and adsorption capacity for odorous compounds and color bodies over a wide range of molecular weights

feature

hydrophilic

manufacturer/tradename

Millistak+®

parameter

2.1 bar max. differential pressure (30 psid) at 37 °C (Forward)
2.1 bar max. differential pressure (30 psid) at 37 °C (Reverse)
2.1 bar max. differential pressure (30 psid) at 4 °C (Forward)

H

14 cm (5.3 in.)

L

22 cm (8.5 in.)

filtration area

0.027 m2

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32mm Round cell window KBr, Undrilled

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Z112178

32mm Round cell window

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material

KBr

material

KBr

material

BaF2

material

NaCl

packaging

pkg of (contains 1 window)

packaging

pkg of (contains 1 window)

packaging

pkg of (contains 1 window)

packaging

pkg of (contains 1 window)

technique(s)

IR spectroscopy: suitable

technique(s)

IR spectroscopy: suitable

technique(s)

IR spectroscopy: suitable

technique(s)

IR spectroscopy: suitable

diam. × thickness

32 mm × 3 mm

diam. × thickness

32 mm × 3 mm

diam. × thickness

32 mm × 3 mm

diam. × thickness

32 mm × 3 mm

General description

product water; post autoclave (1 cycle of 60 minutes at 123 °C) and pure water flush of 10 liters per ft²(100 L/m²) of media surface area

Specifications

Filter Grade: CR40

Preparation Note

Sterilization Method
Integrity is maintained after 2 autoclave cycles of 60 minutes @ 123 °C

Analysis Note

Total organic carbon (TOC) residue: post autoclave (1 cycle of 60 minutes at 123 °C) and pure water flush of 10 liters per ft<sup>2</sup> (100 L/m<sup>2</sup>) of media surface area

Legal Information

MILLISTAK+ is a registered trademark of Merck KGaA, Darmstadt, Germany

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Soonsang Yoon et al.
Journal of neuromuscular diseases, 5(1), 59-73 (2017-12-28)
Mutations in the LAMA2 gene encoding laminin-α2 cause congenital muscular dystrophy Type 1A (MDC1A), a severe recessive disease with no effective treatment. Previous studies have shown that aberrant activation of caspases and cell death through a pathway regulated by BAX
Jessica X Chong et al.
American journal of human genetics, 96(5), 841-849 (2015-05-11)
Multiple pterygium syndrome (MPS) is a phenotypically and genetically heterogeneous group of rare Mendelian conditions characterized by multiple pterygia, scoliosis, and congenital contractures of the limbs. MPS typically segregates as an autosomal-recessive disorder, but rare instances of autosomal-dominant transmission have
Catrin Sian Rutland et al.
Development (Cambridge, England), 138(18), 3955-3966 (2011-08-25)
The expression and function of embryonic myosin heavy chain (eMYH) has not been investigated within the early developing heart. This is despite the knowledge that other structural proteins, such as alpha and beta myosin heavy chains and cardiac alpha actin
Reha M Toydemir et al.
Nature genetics, 38(5), 561-565 (2006-04-28)
The genetic basis of most conditions characterized by congenital contractures is largely unknown. Here we show that mutations in the embryonic myosin heavy chain (MYH3) gene cause Freeman-Sheldon syndrome (FSS), one of the most severe multiple congenital contracture (that is
Sachiko Homma et al.
Skeletal muscle, 6(1), 42-42 (2016-12-03)
Nuclear bodies, such as nucleoli, PML bodies, and SC35 speckles, are dynamic sub-nuclear structures that regulate multiple genetic and epigenetic processes. Additional regulation is provided by RNA/DNA handling proteins, notably TDP-43 and FUS, which have been linked to ALS pathology.

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