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제품정보 (DICE 배송 시 비용 별도)
UNSPSC Code:
41122107
NACRES:
NA.75
eCl@ss:
32190102
Material:
clear , clear bottom, flat bottom , polystyrene plate, round clear wells
Size:
6 wells
Sterility:
sterile
Binding type:
Tissue Culture (TC)-treated surface
Feature:
lid, skirt
material
clear , clear bottom, flat bottom , polystyrene plate, round clear wells
description
growth area 9.5 cm2
sterility
sterile
feature
lid, skirt
packaging
case of 50 (individually wrapped)
manufacturer/tradename
Corning 3516
size
6 wells
well diam.
34.8 mm
well volume
16.8 mL
well working volume
1.9-2.9 mL
binding type
Tissue Culture (TC)-treated surface
General description
Rings on lid prevent cross-contamination. All plates have a uniform footprint and a raised bead to aid stacking. Alphanumerics provide well identification. Polystyrene unless stated otherwise.
Application
Corning® Costar® TC-Treated Multiple Well Plates have been used to:
- cultivate SaOS-2cells
- construct stable cell lines
- seed and differentiate cells for real-time reverse transcription polymerase chain reaction (RT-PCR)
Features and Benefits
- Flat bottoms for enhanced stability.
- Specially treated to promote optimalcell attachment.
- Ensured sterility through gammairradiation.
- Free from pyrogens, ensuring a safe environmentfor cell culture.
Legal Information
Corning is a registered trademark of Corning, Inc.
Costar is a registered trademark of Corning, Inc.
Emad Tolba et al.
Journal of materials chemistry. B, 4(3), 376-386 (2016-01-21)
In human bone, amorphous calcium carbonate (ACC) is formed as a precursor of the crystalline carbonated apatite/hydroxyapatite (HA). Here we describe that the metastable ACC phase can be stabilized by inorganic polyphosphate (polyP) that is also used as a phosphate
Chintha Lankatillake et al.
Plant methods, 17(1), 3-3 (2021-01-08)
Enzyme assays have widespread applications in drug discovery from plants to natural products. The appropriate use of blanks in enzyme assays is important for assay baseline-correction, and the correction of false signals associated with background matrix interferences. However, the blank-correction
S Decembrini et al.
Scientific reports, 10(1), 10275-10275 (2020-06-26)
The development of improved methods to culture retinal organoids is relevant for the investigation of mechanisms of retinal development under pathophysiological conditions, for screening of neuroprotective compounds, and for providing a cellular source for clinical transplantation. We report a tissue-engineering