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SRE0012

Sigma-Aldrich

Apolipoprotein A−I human

histidine-tagged, recombinant, expressed in HEK 293 cells, ≥98% (SDS-PAGE), lyophilized powder

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Synonym(s):
Apolipoprotein A-I histidine-tagged, APOA1, Apo-AI, Apolipoprotein A-I, C117399, MGC117399
CAS Number:
UNSPSC Code:
12352202
NACRES:
NA.26

biological source

human

Quality Level

recombinant

expressed in HEK 293 cells

Assay

≥98% (SDS-PAGE)

form

lyophilized powder

UniProt accession no.

storage temp.

−20°C

Gene Information

human ... APOA1(335)

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Disclaimer

Ce produit, destiné à la recherche scientifique, est soumis à une réglementation spécifique en France, y compris pour les activités d′importation et d′exportation (Article L 1211-1 alinéa 2 du Code de la Santé Publique). L′acheteur (c′est-à-dire l′utilisateur final) est tenu d′obtenir une autorisation d′importation auprès du Ministère français de la Recherche, mentionné à l′article L1245-5-1 II du Code de la Santé Publique. En commandant ce produit, vous confirmez détenir l′autorisation d′importation requise.

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.

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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Nathalie Niyonzima et al.
Journal of immunology (Baltimore, Md. : 1950), 195(1), 257-264 (2015-05-31)
Chronic inflammation of the arterial wall is a key element in the development of atherosclerosis, and cholesterol crystals (CC) that accumulate in plaques are associated with initiation and progression of the disease. We recently revealed a link between the complement
Judit Cubedo et al.
Journal of lipid research, 56(9), 1762-1773 (2015-07-15)
Diabetic (DM) patients have exacerbated atherosclerosis and high CVD burden. Changes in lipid metabolism, lipoprotein structure, and dysfunctional HDL are characteristics of diabetes. Our aim was to investigate whether serum ApoA-I, the main protein in HDL, was biochemically modified in

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