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Key Documents

PEZGS0816

Millipore

Millicell® EZ Slide

8-well glass chamber slide, 0.7 cm2/well, 16/pk, sterile

Synonym(s):

8 well glass slide, Chamber slides

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About This Item

UNSPSC Code:
41104923
eCl@ss:
32011202
NACRES:
NB.22

material

polypropylene wells
soda-lime glass slide

Quality Level

200

sterility

ethylene oxide treated
sterile

feature

Raised corner ridges on the lid facilitate stacking of multiple units

packaging

box of 16 units (4 trays, 4 units/tray)

manufacturer/tradename

Millicell®

technique(s)

cell based assay: suitable
cell culture | mammalian: suitable
immunocytochemistry: suitable

H

13.9 mm , excluding lid
16.2 mm , including lid

L × W × H

75 mm × 25 mm × 1 mm, slide dimensions

L

77.8 mm

W

33.8 mm

size

8 wells

well surface area

0.7 cm2

well volume

200-700 μL

shipped in

ambient

General description

Millicell® EZ Slide allows the user to grow, fix, and stain cells directly on a microscope slide. There is no need to disassemble the unit or transfer cells from one device to another prior to analysis. The polypropylene wells are resistant to most fixatives used, so the cells can be grown on the slide and stained right in the well. Once stained, the microscope slide can be easily removed by pressing down the four side tabs of the unit and lifting the wells off of the slide. This easy slide removal reduces the risk of damaging the cells and no special tools are required to remove the wells from the slide. Raised corner ridges on the cover facilitate stacking of multiple units in the incubator, or they can be incubated in the tray supplied with the units.

Preparation Note

  1. Culture, fix, and stain the cells according to preferred protocol.
  2. To access the microscope slide, hold the Millicell® EZ SLIDE down on a flat surface and break the four tabs by pushing them down with the thumb. Remove the cover. Hold the slide down and lift the wells upward to remove. Remove slide from holder.

Legal Information

Millicell 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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Lulu Hou et al.
Investigative ophthalmology & visual science, 61(5), 7-7 (2020-05-12)
To investigate the effect and mechanism of Agrin on limbal stem cell proliferation and corneal wound healing. Limbal stem cells were isolated and treated with different concentrations of Agrin. CCK-8 and cell proliferation markers (Ki67 and pH3) were detected to
Guang-Chun Wang et al.
Journal of inflammation (London, England), 17, 2-2 (2020-01-09)
The relationship between chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) and erectile dysfunction (ED) has been shown in many studies. However, the specific mechanism remains unclear. This study was to investigate the corpus cavernosum smooth muscle cell function and phenotype transformation
Anna A Kondratova et al.
The EMBO journal, 39(11), e101573-e101573 (2020-04-24)
High expression of 2',5'-oligoadenylate synthetase 1 (OAS1), which adds AMP residues in 2',5' linkage to a variety of substrates, is observed in many cancers as a part of the interferon-related DNA damage resistance signature (IRDS). Poly(ADP-ribose) (PAR) is rapidly synthesized
Vahid Rajabali Zadeh et al.
The Journal of general virology, 101(6), 573-586 (2020-05-08)
Bone marrow stromal cell antigen-2 (BST-2), also known as tetherin, is an interferon-inducible membrane-associated protein. It effectively targets enveloped viruses at the release step of progeny viruses from host cells, thereby restricting the further spread of viral infection. Junin virus
Slim Mzoughi et al.
Science advances, 6(2), eaax9852-eaax9852 (2020-01-18)
Holoprosencephaly (HPE) is a congenital forebrain defect often associated with embryonic lethality and lifelong disabilities. Currently, therapeutic and diagnostic options are limited by lack of knowledge of potential disease-causing mutations. We have identified a new mutation in the PRDM15 gene
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