S5519
Lipoprotein Deficient Serum from human plasma
sterile-filtered, frozen liquid
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About This Item
Codice UNSPSC:
12352202
NACRES:
NA.26
Prodotti consigliati
Origine biologica
human
Livello qualitativo
Sterilità
sterile-filtered
Stato
frozen liquid
Qualità
No banding correlating to lipoprotein observed by Agarose Electrophoresis
Composizione
protein, ≥50 mg/mL biuret
Origine
USA origin
Concentrazione
≥50 mg protein/mL Biuret
tecniche
cell culture | mammalian: suitable
Condizioni di spedizione
dry ice
Temperatura di conservazione
−20°C
Informazioni sul gene
human ... APOA1(335) , APOA4(337) , APOA5(116519) , APOB(338) , APOC1(341) , APOC3(345) , APOE(348)
Azioni biochim/fisiol
Lipoprotein deficient serum was shown to inhibit the transfer of unesterified cholesterol from LDL to HDL.
Nota sulla preparazione
Dialyzed against Dulbecco′s phosphate buffered saline, pH 7.2-7.3
Esclusione di responsabilità
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.
Codice della classe di stoccaggio
10 - Combustible liquids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
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I clienti hanno visto anche
E Velazquez et al.
Biomedica biochimica acta, 50(9), 1109-1114 (1991-01-01)
The in vitro transfer of radiolabelled unesterified cholesterol from human low- and very low- to high-density lipoproteins in the presence of either lipoprotein deficient serum or bovine serum albumin has been studied. The rate of transfer was faster from LDL
Inés Pineda Torra et al.
Molecular and cellular biology, 28(8), 2626-2636 (2008-02-06)
Dysregulation of liver X receptor alpha (LXRalpha) activity has been linked to cardiovascular and metabolic diseases. Here, we show that LXRalpha target gene selectivity is achieved by modulation of LXRalpha phosphorylation. Under basal conditions, LXRalpha is phosphorylated at S198; phosphorylation
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