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H8898

Sigma-Aldrich

Halocarbon oil 700

Synonym(s):

Chlorotrifluoroethene homopolymer

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About This Item

CAS Number:
9002-83-9
MDL number:
MFCD00147324
UNSPSC Code:
12162002
PubChem Substance ID:
24895833
NACRES:
NA.75

form

liquid

InChI

1S/C2ClF3/c3-1(4)2(5)6

InChI key

UUAGAQFQZIEFAH-UHFFFAOYSA-N

General description

Halocarbon oil 700 is used for mounting worms on agarose pads. It facilitates movement of worms for microscopic view. The halocarbon acts as a source of oxygen and blocks desiccation during optical digital embryo sampling.

Application

Halocarbon oil 700 has been used:
  • to facilitate piercing of vitelline membranes with a glass capillary to make small holes on spider embryos
  • in microinjection procedure to track the vesicular stomatitis virus infection in Caenorhabditis elegans
  • for live imaging of embryo sample using Zeiss LSM710 confocal system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

H8898-50ML:
H8898-BULK:
H8898-VAR:
H8898-100ML:

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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Infection of Caenorhabditis elegans with Vesicular Stomatitis Virus via Microinjection
Martin A, et al.
Bio-protocol, 7(22) (2017)
Multi-color FISH facilitates analysis of cell-type diversification and developmental gene regulation in the Parasteatoda spider embryo
Akiyama-Oda Y and Oda H
Development, Growth & Differentiation, 58(2), 215-224 (2016)
C. elegans: A Practical Approach, 81-81 (1999)
Lunhao Chen et al.
Frontiers in neuroscience, 12, 324-324 (2018-06-06)
Here we described an experimental protocol for in vivo imaging of macropinocytosis and subsequent intracellular events. By microinjection, we delivered fluorescence dextrans together with or without ATPγS into transparent Drosophila melanogaster embryos. Using a confocal microscope for live imaging, we
Drosophila melanogaster: Practical Uses in Cell and Molecular Biology, 514-514 (1995)
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