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C-12202

Sigma-Aldrich

Human Umbilical Artery Endothelial Cells (HUAEC)

500,000 cryopreserved cells

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250 MG
₩188,080
1 G
₩566,066

About This Item

UNSPSC Code:
41106514
NACRES:
NA.81

₩188,080


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biological source

human umbilical cord artery

packaging

pkg of 500,000 cells

morphology

( endothelial)

technique(s)

cell culture | mammalian: suitable

shipped in

dry ice

storage temp.

−196°C

General description

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Cell Line Origin

Artery

Application

Primary Human Umbilical Artery Endothelial Cells (HUAEC) are isolated from the arteries of the umbilical cord and are provided in a cryopreserved format. They are often used for in vitro studies on atherosclerosis but also for endothelial cell-dependent lymphocyte activation and chemoattractant activity experiments. (Human Umbilical Vein Endothelial Cells (HUVEC) from the same donor are available on request).

Quality

Rigid quality control tests are performed for each lot of Endothelial Cells from large vessels. They are tested for cell morphology, adherence rate, and cell viability. Flow cytometric analyses for cell-type specific markers, e.g. von Willebrand Factor (vWF) and CD31, as well as Dil-Ac-LDL uptake assays are also carried out for each lot. Growth performance is tested through multiple passages up to 15 population doublings (PD) under culture conditions without antibiotics and antimycotics. In addition, all cells have been tested for the absence of HIV-1, HIV-2, HBV, HCV, HTLV-1, HTLV-2 and microbial contaminants (fungi, bacteria, and mycoplasma).

Warning

Although tested negative for HIV-1, HIV-2, HBV, HCV, HTLV-1 and HTLV-2, the cells – like all products of human origin – should be handled as potentially infectious. No test procedure can completely guarantee the absence of infectious agents.

Subculture Routine

Click here for more information.

Other Notes

Recommended Plating Density: 5000 - 10000 cells per cm2Passage After Thawing: P1Tested Markers: von Willebrand Factor (vWF) positive, CD31 positive, Dil-Ac-LDL uptake positiveGuaranteed population doublings: >15

Recommended products

Recommended Primary Cell Culture Media:Link

Disclaimer

RESEARCH USE ONLY. This product is regulated in France when intended to be used for scientific purposes, including for import and export activities (Article L 1211-1 paragraph 2 of the Public Health Code). The purchaser (i.e. enduser) is required to obtain an import authorization from the France Ministry of Research referred in the Article L1245-5-1 II. of Public Health Code. By ordering this product, you are confirming that you have obtained the proper import authorization.

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This Item
67213067192470023
mol wt

Mp 3,000

mol wt

Mp 5,000

mol wt

Mp 10,000

mol wt

-

reaction suitability

reagent type: cross-linking reagent

reaction suitability

-

reaction suitability

-

reaction suitability

reagent type: cross-linking reagent

Ω-end

hydroxyl

Ω-end

hydroxyl

Ω-end

hydroxyl

Ω-end

-

α-end

amine

α-end

amine

α-end

amine

α-end

-

Quality Level

100

Quality Level

200

Quality Level

100

Quality Level

100


Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable



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    Jeremiah A Johnson et al.
    Macromolecules, 43(24), 10326-10335 (2011-05-03)
    Graft-through ring-opening metathesis polymerization (ROMP) using ruthenium N-heterocyclic carbene catalysts has enabled the synthesis of bottle-brush polymers with unprecedented ease and control. Here we report the first bivalent-brush polymers; these materials were prepared by graft-through ROMP of drug-loaded polyethylene-glycol (PEG)
    Angela X Gao et al.
    ACS macro letters, 3(9), 854-857 (2014-09-23)
    A panel of acid-labile bis-norbornene cross-linkers was synthesized and evaluated for the formation of acid-degradable brush-arm star polymers (BASPs) via the brush-first ring-opening metathesis polymerization (ROMP) method. An acetal-based cross-linker was identified that, when employed in conjunction with a poly(ethylene
    Folic acid-decorated and PEGylated PLGA nanoparticles for improving the antitumour activity of 5-fluorouracil.
    El-Hammadi
    International Journal of Pharmaceutics, 516(1-2), 61-70 (2017)