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SCNY00100

Millipore

Millipore® Steriflip® Vacuum Tube Top Filter

pore size 100.0 μm, Nylon membrane (net), funnel capacity 50 mL, pack of 25 ea

Synonym(s):

Steriflip® Nylon Net Sterile Centrifuge Tube Top Filter Unit, tube top sterile filter unit, tube top vacuum filter, tube top vacuum sterile filtering unit

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About This Item

UNSPSC Code:
41104914
eCl@ss:
32031602
NACRES:
NB.22

material

Nylon membrane (net)
acrylic housing
polypropylene

Quality Level

400

sterility

sterile

product line

Steriflip®

feature

holdup volume 0.6 mL
hydrophilic

packaging

pack of 25 ea

parameter

45 °C max. temp.

technique(s)

sterile filtration: suitable

H

138 mm

diam.

6.4 cm

filter diam.

4 cm

filtration area

7 cm2

funnel capacity

50 mL

pore size

100.0 μm pore size

fitting

double lead thread inlet (with vacuum port)
 double lead thread outlet for 50 mL centrifuge tube

shipped in

ambient

Related Categories

General description

Steriflip® filtration devices allow the separation of larger volumes of cellular material with the added advantage of maintaining a sterile environment ensuring sample sterility, an option that open-top gravity flow filter devices cannot guarantee. Steriflip Sterile Centrifuge Tube Top Filter Unit permits the passage of cells while retaining large tissue clumps. This improves recovery and reduces the time to collect the isolated cells.

Application

For Research Use Only.
Steriflip® Sterile Centrifuge Tube Top Filter Unit has been used in tumor procurement and processing. It has also been used in the isolation of cardiac stem cells (CSCs) from the extracted hearts of Balb/c mice.

Legal Information

Millipore is a registered trademark of Merck KGaA, Darmstadt, Germany
Steriflip is a registered trademark of Merck KGaA, Darmstadt, Germany

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Jingjin Liu et al.
Experimental and therapeutic medicine, 13(6), 3348-3354 (2017-06-08)
Cardiac stem cells (CSCs) are the most promising and effective candidates for the therapy of cardiac regenerative diseases; however, they have marked limitations. For instance, the implantation of CSCs is hampered by factors such as their sustainability and long-term durability.
Steven D Forsythe et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 27(18), 5141-5150 (2021-07-03)
Immunotherapy efficacy data on appendiceal cancer from clinical trials does not exist, due to appendiceal cancer incidence of 0.97 per 100,000. The goal of this study was to preclinically explore the application of immunotherapy in treating appendiceal cancer in a
Steven Forsythe et al.
Annals of biomedical engineering, 48(3), 940-952 (2019-04-26)
Colorectal cancer is subject to a high rate of mutations, with late stage tumors often containing many mutations. These tumors are difficult to treat, and even with the recently implemented methods of personalized medicine at modern hospitals aiming to narrow
Steven D Forsythe et al.
Annals of surgical oncology, 27(13), 4950-4960 (2020-07-08)
Chemotherapy dosing duration and perfusion temperature vary significantly in HIPEC protocols. This study investigates patient-derived tumor organoids as a platform to identify the most efficacious perfusion protocol in a personalized approach. Peritoneal tumor tissue from 15 appendiceal and 8 colon

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