产品名称
MF-Millipore™ 膜过滤装置, 0.8 µm 孔径，网格, MF-Millipore™, filter diam. 25 mm, hydrophilic, black, gridded
material
black filter
gridded
mixed cellulose esters (MCE) membrane
description
25 mm diameter, mixed cellulose esters (MCE) membrane, hydrophilic, black, gridded, 100 discs
sterility
non-sterile
feature
hydrophilic
manufacturer/tradename
MF-Millipore™
Millipore
sustainability
Greener Alternative Product
parameter
16 L/min-cm2 air flow rate
190 mL/min-cm2 water flow rate
75 °C max. temp.
diam.
25 mm
filter diam.
25 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
greener alternative category
shipped in
ambient
Quality Level
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Application
- 荧光测定
- 颗粒监测
- 空气监测
- 微塑料
Features and Benefits
- 适用于生物和环境样品。
- 可选择不同孔径，黑色或白色。
- 可高压灭菌，与环氧乙烷和伽马辐射相容
General description
MF-Millipore™膜滤器包括醋酸纤维素和硝酸纤维素。它广泛用于分析和研究应用。
我们竭诚为您带来经过重新设计的绿色替代产品，实现可持续性更高的研究方案。滤膜的内盒&外盒均由遵循ISCC质量平衡分配的生物循环材料制成。 点击此处以获取更多信息。
Legal Information
MF-Millipore is a trademark of Merck KGaA, Darmstadt, Germany
signalword
Danger
hcodes
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 2 - Eye Irrit. 2 - Flam. Sol. 1
存储类别
4.1B - Flammable solid hazardous materials
wgk
WGK 3
Tomofumi Oga et al.
Frontiers in neural circuits, 10, 74-74 (2016-10-07)
Neurons in the mammalian primary visual cortex (V1) are systematically arranged across the cortical surface according to the location of their receptive fields (RFs), forming a visuotopic (or retinotopic) map. Within this map, the foveal visual field is represented by
Tomofumi Oga et al.
Frontiers in neuroscience, 11, 118-118 (2017-03-30)
Pyramidal cells in the primate cerebral cortex, particularly those in layer III, exhibit regional variation in both the time course and magnitude of postnatal growth and pruning of dendrites and spines. Less is known about the development of pyramidal cell
Tatsuya Ueno et al.
Neurobiology of disease, 64, 142-149 (2014-01-09)
Levodopa-induced dyskinesia (LID) is a major complication of long-term dopamine replacement therapy for Parkinson's disease, and becomes increasingly problematic in the advanced stage of the disease. Although the cause of LID still remains unclear, there is accumulating evidence from animal
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