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Merck
CN

56822

浸镜油

suitable for microscopy

别名:

光学显微镜用浸镜油

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关于此项目

UNSPSC Code:
12171500
NACRES:
NA.47
MDL number:
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产品名称

浸镜油, suitable for microscopy

biological source

synthetic

form

liquid

refractive index

n20/D 1.516

viscosity

100-120 mPa.s(20 °C)

density

1.025 g/mL at 20 °C

suitability

suitable for microscopy

application(s)

hematology
histology

storage temp.

room temp

Quality Level

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Application

浸泡油用于高分辨率(1000倍)光学显微镜工作,与油浸泡物镜结合使用,以在固定、嵌入、染色或反染色和安装后优化组织学、细胞学、血液学和细菌标本材料的显微检查。

Biochem/physiol Actions

将浸镜油滴加到染色的已安装或未安装的试样材料上,在试样与显微镜透镜之间形成一层透明膜,以消除入射光的偏转,从而大大提高透镜的光学效率。

General description

浸镜油是一种透明、粘稠的液体,具有优化的折射率,经过专门改性,使其尽可能接近玻璃的折射率(RI) (ne = 1.5)。将它与物镜配合使用,可提高分辨率。

Features and Benefits

  • Immersion oil for general use in light microscopy.
  • Excellent, defined refractive index eliminates refractive distortion.
  • Engineered for optimal viscosity and homogeneity.
  • Good UV transmission and low residual fluorescence.

wgk

WGK 2

pictograms

Environment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 2

存储类别

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

监管及禁止进口产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Theis Sommer et al.
Scientific reports, 8(1), 13104-13104 (2018-09-01)
The catalytic mechanism of the cyclic amidohydrolase isatin hydrolase depends on a catalytically active manganese in the substrate-binding pocket. The Mn2+ ion is bound by a motif also present in other metal dependent hydrolases like the bacterial kynurenine formamidase. The
Thomas P Burghardt et al.
Applied optics, 48(32), 6120-6131 (2009-11-12)
Total internal reflection fluorescence (TIRF) microscopy uses the evanescent field on the aqueous side of a glass/aqueous interface to selectively illuminate fluorophores within approximately 100 nm of the interface. Applications of the method include epi-illumination TIRF, where the exciting light
P L Appleton et al.
Journal of microscopy, 234(2), 196-204 (2009-04-29)
Visualizing overall tissue architecture in three dimensions is fundamental for validating and integrating biochemical, cell biological and visual data from less complex systems such as cultured cells. Here, we describe a method to generate high-resolution three-dimensional image data of intact

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